Small Molecule & Simulation
Kinase selectivity, non-standard force-field parameters, and purchasable focused libraries converge on a finite experimental decision.
Explore Small Molecule & Simulation →19 CAT solutions
Convert molecular, omics, imaging, and materials data into calibrated shortlists, constrained experimental portfolios, and traceable delivery packages.
HLA-I/HLA-II presentation, clonality, tumor expression, immunogenicity, manufacturability, and junction risk are evaluated separately before a constrained portfolio is assembled.
Kinase selectivity, non-standard force-field parameters, and purchasable focused libraries converge on a finite experimental decision.
Explore Small Molecule & Simulation →19 CAT solutionsStructural, evolutionary, safety, immunogenicity, and manufacturability evidence is combined into experiment-ready biologic designs.
Explore Biologics Design →19 CAT solutionsVersion-controlled variant, transcript, HLA, and editing evidence is compiled into validation queues, guide sets, and therapeutic payloads.
Explore Genomics & Editing →24 CAT solutionsReference mapping, tissue safety, translational deconvolution, model audit, and immune-repertoire analysis are delivered with explicit validation gates.
Explore Single-cell & Tissue →26 CAT solutionssiRNA, ASO, mRNA, circRNA, and aptamer programs use modality-specific efficacy, safety, manufacturability, and assay constraints.
Explore Nucleic Acid Therapeutics →22 CAT solutionsIHC, multiplex pathology, H&E, spatial transcriptomics, MRI/CT, response imaging, and multimodal registration produce auditable regions, phenotypes, and validation panels.
Explore Bioimaging & Spatial Biology →24 CAT solutionsMachine-learning potentials, electronic structure, adsorption, interfaces, crystals, and electrochemistry narrow compositions and structures to experimentally tractable sets.
Explore AI-guided Materials R&D →24 CAT solutionsEvery CAT entry has a defined target, candidate funnel, evidence framework, execution plan, and downstream experimental endpoint.
Advance selective compounds and simulation-ready chemical assets.
MOL-PAR-001Covalent-warhead Parameter PlatformProject-defined target and comparator setMOL-PAR-ACR-001Acrylamide–Cysteine Parameter PackageDedicated route under MOL-PAR-001MOL-PAR-CYA-001Cyanoacrylamide Reversible-covalent Parameter PackageDedicated route under MOL-PAR-001MOL-PAR-SUF-001Sulfonyl-fluoride Residue-selective Parameter PackageDedicated route under MOL-PAR-001MOL-PAR-0022'-OMe, 2'-F, 2'-MOE, LNA, PS — Simulation-ready Force-field Parameters2'-OMe, 2'-F, 2'-MOE, LNA, PSMOL-PAR-003LNPSM-102, ALC-0315, MC3, C12-200MOL-PAR-004p Ser/p Thr/p Tyr, acK, meK — Simulation-ready Force-field Parametersp Ser/p Thr/p Tyr, acK, meKMOL-PAR-005Zn, Mg, Fe-heme, Cu, Mn — Simulation-ready Force-field ParametersZn, Mg, Fe-heme, Cu, MnMOL-PAR-006ADC linker-payloadvc-PAB, GGFG, MMAE, Dxd, DM1BIO-PEV-001Industrial Enzyme Activity–Stability Libraryω-/KRED and related targetsBIO-PEV-002Antibody Affinity–Expression LibraryIgG/VHH CDR and sitesBIO-PEV-003PETase Thermostability Variant LibraryPETase/FAST-PETaseBIO-PEV-004Cas9 Specificity Variant LibrarySp Cas9/Cas12aBIO-PEV-005Therapeutic Enzyme Stability–Immunogenicity LibraryProject-defined target and comparator setSelect sequences, chemistries, and construct architectures.
IMG-IHC-001Breast Cancer CD8 IHC Spatial QuantificationCD8+ cells × OncologyIMG-IHC-002PD-L1 TPS/CPS Computation and ReviewPD-L1 IHC × Oncologycells/cellsIMG-IHC-003HER2 Heterogeneity and Membrane-completeness AnalysisHER2 IHC × regionsIMG-IHC-004Multiplex IHC Immune-neighborhood AnalysisCD8/CD4/FOXP3/CD68/PanCKIMG-SPX-001Colorectal Cancer Immune–Tumor Boundary AtlasCRC tumor/adjacent Visium + scRNA referenceIMG-SPX-002Breast Cancer Immune-exclusion Nichebreast tumor spatial RNA + H&E + IHCIMG-SPX-003Liver Fibrosis Spatial Zonationfibrotic liver zonation + stellate/macrophage statesIMG-SPX-004Neuroinflammatory Cell Neighborhoodsbrain spatial transcriptomics + glial referenceIMG-HST-001H&E Immune-hot/Cold Phenotypebreast/NSCLC H&E + immune labelsIMG-HST-002Research-use Colorectal MSI PrescreenCRC H&E + MSI statusIMG-HST-003Digital Morphology Score for Liver Fibrosisliver biopsy H&E/trichromeIMG-HST-004Tumor Necrosis and Treatment-effect Quantificationresection H&E pre/post therapyIMG-RSP-001Breast Cancer Neoadjuvant DCE-MRI Early Responsebaseline/early-treatment DCE-MRI × pCR/RCBIMG-RSP-002ICI Lesion-level Response and Pseudoprogressionserial CT × lesion response × immune outcomesIMG-RSP-003ADC Treatment-response Imaging Heterogeneityserial CT/MRI × lesion-level responseIMG-RSP-004Drug Longitudinal Tissue Imagingpaired biopsy/SHG/MRIIMG-REG-001H&E–IHC– Trimodal Registrationserial sections/same-slide multimodal tissueIMG-REG-002MRI– slides Spatial Bridgingresection specimen × ex vivo/in vivo MRIIMG-REG-003cells Reference MappingIMC/CODEX × scRNA referenceIMG-REG-004Drug regions Cross-modal Validationspatial RNA × phospho-IHC × morphologyKinase selectivity, non-standard force-field parameters, and purchasable focused libraries converge on a finite experimental decision.
Turns ·/·Selectivity evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns ·Focused Library evidence into a capacity-matched experimental package.
Open product line →Structural, evolutionary, safety, immunogenicity, and manufacturability evidence is combined into experiment-ready biologic designs.
Turns ·/cells· evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Version-controlled variant, transcript, HLA, and editing evidence is compiled into validation queues, guide sets, and therapeutic payloads.
Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns ·structures evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Reference mapping, tissue safety, translational deconvolution, model audit, and immune-repertoire analysis are delivered with explicit validation gates.
Turns cells·Reference Atlas evidence into a capacity-matched experimental package.
Open product line →Turns cells· evidence into a capacity-matched experimental package.
Open product line →Turns cells· evidence into a capacity-matched experimental package.
Open product line →Turns cells· evidence into a capacity-matched experimental package.
Open product line →Turns cells·Model Audit evidence into a capacity-matched experimental package.
Open product line →Turns cells· evidence into a capacity-matched experimental package.
Open product line →siRNA, ASO, mRNA, circRNA, and aptamer programs use modality-specific efficacy, safety, manufacturability, and assay constraints.
Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →IHC, multiplex pathology, H&E, spatial transcriptomics, MRI/CT, response imaging, and multimodal registration produce auditable regions, phenotypes, and validation panels.
Turns ·cellsand evidence into a capacity-matched experimental package.
Open product line →Turns ·statesandneighborhoods evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns · evidence into a capacity-matched experimental package.
Open product line →Turns ·Spatial Bridging evidence into a capacity-matched experimental package.
Open product line →Machine-learning potentials, electronic structure, adsorption, interfaces, crystals, and electrochemistry narrow compositions and structures to experimentally tractable sets.
Turns Catalysisand Catalysis evidence into a capacity-matched experimental package.
Open product line →Turns Catalysisand Catalysis evidence into a capacity-matched experimental package.
Open product line →Turns Catalysisand Catalysis evidence into a capacity-matched experimental package.
Open product line →Turns Materialsand evidence into a capacity-matched experimental package.
Open product line →Turns Materialsand evidence into a capacity-matched experimental package.
Open product line →Turns Materialsand evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns ai-guided materials r&d evidence into a capacity-matched experimental package.
Open product line →Turns ai-guided materials r&d evidence into a capacity-matched experimental package.
Open product line →Turns surfaces· · evidence into a capacity-matched experimental package.
Open product line →Turns surfaces· · evidence into a capacity-matched experimental package.
Open product line →Turns surfaces· · evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns and evidence into a capacity-matched experimental package.
Open product line →Turns ·MOF· evidence into a capacity-matched experimental package.
Open product line →Turns ·MOF· evidence into a capacity-matched experimental package.
Open product line →Turns ·MOF· evidence into a capacity-matched experimental package.
Open product line →Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
SDF/CSV/Parquet/PDB/HTML/JSON
MethodsKLIFS, RDKit, smina, gnina, ProLIF, MDAnalysis
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
MOL-KIN-001CDK9 vs. CDK2/7/12
1,284 compounds → 8 advancement candidates → 6 counter-screen targetsOpen solution →MOL-KIN-002JAK1 vs. JAK2/JAK3/TYK2
960 compounds → 9 advancement candidates → 5 counter-screen targetsOpen solution →MOL-KIN-003BTK vs. TEC/BMX/ITK
742 compounds → 7 advancement candidates → 5 counter-screen targetsOpen solution →MOL-KIN-004PI3Kα vs. PI3Kβ/δ/γ
1,116 compounds → 10 advancement candidates → 6 counter-screen targetsOpen solution →MOL-KIN-005CDK4/6 vs. CDK2/9
884 compounds → 8 advancement candidates → 4 counter-screen targetsOpen solution →Small Molecule & Simulation research and development
1,284 compounds → 8 advancement candidates → 6 counter-screen targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CDK9 vs. CDK2/7/12, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to kinase selectivity design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and
960 compounds → 9 advancement candidates → 5 counter-screen targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define JAK1 vs. JAK2/JAK3/TYK2, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to kinase selectivity design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
B cells
742 compounds → 7 advancement candidates → 5 counter-screen targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define BTK vs. TEC/BMX/ITK, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to kinase selectivity design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for B cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncologyand
1,116 compounds → 10 advancement candidates → 6 counter-screen targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PI3Kα vs. PI3Kβ/δ/γ, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to kinase selectivity design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncologyand.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
cells
884 compounds → 8 advancement candidates → 4 counter-screen targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CDK4/6 vs. CDK2/9, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to kinase selectivity design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
frcmod/mol2/itp/offxml/XML/SDF/JSON/HTML
MethodsAmber Tools, OpenFF, GROMACS, OpenMM, Parm Ed
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
MOL-PAR-001Project-defined target and comparator set
3 → 3 →Open solution →MOL-PAR-0022'-OMe, 2'-F, 2'-MOE, LNA, PS
18 → → 4 engine formatsOpen solution →MOL-PAR-003SM-102, ALC-0315, MC3, C12-200
12 → pH states → all-atom/coarse-grained versionsOpen solution →MOL-PAR-004p Ser/p Thr/p Tyr, acK, meK
24 → protonation calibration → protein example systemOpen solution →MOL-PAR-005Zn, Mg, Fe-heme, Cu, Mn
8 →/→ validationOpen solution →MOL-PAR-006vc-PAB, GGFG, MMAE, Dxd, DM1
20 linker/payload → →Open solution →Small Molecule & Simulation research and development
3 → 3 →
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Small Molecule & Simulation research and development
12 adducts → 2 charge/torsion routes → 5 engine formats
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Acrylamide–Cys Michael, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Small Molecule & Simulation research and development
8 free/adduct pairs → 2 state models → 5 engine formats
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Cyanoacrylamide–Cys states, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
SuFEx and
16 warhead–residue combinations → 4 adduct templates → 5 engine formats
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Sulfonyl fluoride and Lys/Tyr/Ser/Cys, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for SuFEx and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
siRNA/ASO/mRNA
18 → → 4 engine formats
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 2'-OMe, 2'-F, 2'-MOE, LNA, PS, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for siRNA/ASO/mRNA.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Deliveryand Vaccine
12 → pH states → all-atom/coarse-grained versions
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SM-102, ALC-0315, MC3, C12-200, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Deliveryand Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and
24 → protonation calibration → protein example system
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define p Ser/p Thr/p Tyr, acK, meK, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and CYP
8 →/→ validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Zn, Mg, Fe-heme, Cu, Mn, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and CYP.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC and Bioconjugation
20 linker/payload → →
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define vc-PAB, GGFG, MMAE, Dxd, DM1, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to simulation-ready force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC and Bioconjugation.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
XLSX/SDF/SMILES/PDBQT/Parquet/HTML
MethodsRDKit, Data Warrior, smina, ProLIF, Datamol
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
MOL-FOC-001KRAS G12D Switch-II pocket
50,000 candidates → 1,800 designs → 120Open solution →MOL-FOC-002WRN helicase/ATPase
32,000 candidates → 1,500 designs → 96Open solution →MOL-FOC-003PRMT5 MTA-cooperative pocket
28,000 candidates → 1,400 designs → 82Open solution →MOL-FOC-004TEAD1/4
20,000 candidates → 1,200 designs → 74Open solution →MOL-FOC-005SHP2 allosteric pocket
36,000 candidates → 1,600 designs → 105Open solution →KRAS
50,000 candidates → 1,800 designs → 120
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define KRAS G12D Switch-II pocket, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target-focused purchasable libraries.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for KRAS.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Small Molecule & Simulation research and development
32,000 candidates → 1,500 designs → 96
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define WRN helicase/ATPase, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target-focused purchasable libraries.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Small Molecule & Simulation research and development
28,000 candidates → 1,400 designs → 82
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PRMT5 MTA-cooperative pocket, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target-focused purchasable libraries.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Hippo
20,000 candidates → 1,200 designs → 74
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define TEAD1/4, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target-focused purchasable libraries.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Hippo.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Small Molecule & Simulation research and development
36,000 candidates → 1,600 designs → 105
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SHP2 allosteric pocket, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target-focused purchasable libraries.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Small Molecule & Simulation research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
PDB/mmCIF/FASTA/CSV/Parquet/HTML/XLSX
MethodsCELLxGENE, HPA, Scanpy, PyMOL, ANARCI, Boltz
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
BIO-SEP-001TROP2/TACSTD2
58 surface patches → 4 epitopes → 4/validationOpen solution →BIO-SEP-002CLDN18.2 loops
34 surface patches → 4 epitopes → 3/validationOpen solution →BIO-SEP-0034Ig-B7-H3/CD276
64 surface patches → 5 epitopes → 3 competition assaysOpen solution →BIO-SEP-004GPC3
49 surface patches → 4 epitopes → 4 validationOpen solution →BIO-SEP-005DLL3
41 surface patches → 3 epitopes → 3 Neuro validationOpen solution →BIO-SEP-006GPRC5D
38 surface patches → 4 epitopes → 4/NeurovalidationOpen solution →ADC/TCE
58 surface patches → 4 epitopes → 4/validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define TROP2/TACSTD2, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC/TCE.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
CAR-T/ADC
34 surface patches → 4 epitopes → 3/validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CLDN18.2 loops, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for CAR-T/ADC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC
64 surface patches → 5 epitopes → 3 competition assays
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 4Ig-B7-H3/CD276, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Liver Cancer CAR-T/TCE
49 surface patches → 4 epitopes → 4 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define GPC3, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Liver Cancer CAR-T/TCE.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
SCLC ADC/TCE
41 surface patches → 3 epitopes → 3 Neuro validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define DLL3, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for SCLC ADC/TCE.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
38 surface patches → 4 epitopes → 4/Neurovalidation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define GPRC5D, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to target–epitope safety design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/CSV/Parquet/PDB/HTML
MethodsESM, FoldX, Rosetta, ProteinMPNN, PyMOL
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
BIO-PEV-001ω-/KRED and related targets
3,842 designs → 88 variants + 8 controls → 96 wellsOpen solution →BIO-PEV-002IgG/VHH CDR and sites
2,460 designs → 80 variants + 16 controls → 96 wellsOpen solution →BIO-PEV-003PETase/FAST-PETase
5,120 designs → 88 variants + 8 controls → 96 wellsOpen solution →BIO-PEV-004Sp Cas9/Cas12a
4,320 designs → 84 variants + 12 controls → 96 wellsOpen solution →BIO-PEV-005Project-defined target and comparator set
2,980 designs → 72 variants + 24 controls → 96 wellsOpen solution →Biologics Design research and development
3,842 designs → 88 variants + 8 controls → 96 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define ω-/KRED and related targets, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to protein variant library design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
2,460 designs → 80 variants + 16 controls → 96 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define IgG/VHH CDR and sites, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to protein variant library design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
5,120 designs → 88 variants + 8 controls → 96 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PETase/FAST-PETase, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to protein variant library design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
4,320 designs → 84 variants + 12 controls → 96 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Sp Cas9/Cas12a, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to protein variant library design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
2,980 designs → 72 variants + 24 controls → 96 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to protein variant library design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/PDB/CSV/Parquet/HTML/XLSX
MethodsANARCI, PROPKA, FreeSASA, Colab Fold, pandas
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
BIO-DEV-00110–30 IgG candidates
24 candidates → 6 advancement candidates → 4 CMCOpen solution →BIO-DEV-002Cross Mab/KiH/IgG-sc Fv
16 configurations → 4 advancement candidates → 5 riskOpen solution →BIO-DEV-003VHH/nanobody
32 candidates → 8 advancement candidates → 4Open solution →BIO-DEV-004IgG + sitescandidates
18/sitesdesigns → 5 advancement candidates → DAR/Open solution →Biologics Design research and development
24 candidates → 6 advancement candidates → 4 CMC
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 10–30 IgG candidates, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to antibody developability triage.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
16 configurations → 4 advancement candidates → 5 risk
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Cross Mab/KiH/IgG-sc Fv, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to antibody developability triage.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
32 candidates → 8 advancement candidates → 4
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define VHH/nanobody, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to antibody developability triage.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC
18/sitesdesigns → 5 advancement candidates → DAR/
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define IgG + sitescandidates, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to antibody developability triage.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/CSV/PDB/HTML/XLSX
MethodsNetMHCIIpan, MHCflurry, IEDB, ANARCI, FoldX
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
BIO-DIM-001Project-defined target and comparator set
27 → 42 → 8 constructsOpen solution →BIO-DIM-002VHH
18 → 36 → 6 constructsOpen solution →BIO-DIM-003AAV variants
31 → 48 → 10 constructsOpen solution →BIO-DIM-00420–80 aa
12 → 24 → 6 constructsOpen solution →Biologics Design research and development
27 → 42 → 8 constructs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to de-immunized construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
18 → 36 → 6 constructs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define VHH, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to de-immunized construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Gene Therapy
31 → 48 → 10 constructs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define AAV variants, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to de-immunized construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Gene Therapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Biologics Design research and development
12 → 24 → 6 constructs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 20–80 aa, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to de-immunized construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Biologics Design research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
VCF/TSV/Parquet/JSON/DuckDB/HTML
MethodsVEP, OpenCRAVAT, bcftools, DuckDB, FoldX
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-VAR-001EGFR/KRAS/TP53/PIK3CA and related targets
486 VUS → 18 → 6Open solution →GEN-VAR-002CFTR/DMD/HBB/F8/F9 and related targets
324 VUS → 16 → 5/validationOpen solution →GEN-VAR-003BRCA1/2 + MMR genes
188 VUS → 12 → 4 validationOpen solution →GEN-VAR-004UTR
742 → 20 candidates → 8Open solution →Oncology panel
486 VUS → 18 → 6
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define EGFR/KRAS/TP53/PIK3CA and related targets, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to vus triage and validation queue.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology panel.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Inherited Disease
324 VUS → 16 → 5/validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CFTR/DMD/HBB/F8/F9 and related targets, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to vus triage and validation queue.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Inherited Disease.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology
188 VUS → 12 → 4 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define BRCA1/2 + MMR genes, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to vus triage and validation queue.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and Gene Therapy
742 → 20 candidates → 8
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define UTR, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to vus triage and validation queue.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and Gene Therapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
VCF/TSV/JSON/CSV/HTML
MethodsPharmCAT, Aldy, Stargazer, VEP
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-PGX-001CYP2D6 SNV/CNV/hybrid
128 samples → 19 → 8Open solution →GEN-PGX-002DPYD
86 samples → 7 risk → 4Open solution →GEN-PGX-003TPMT + NUDT15
112 samples → 9 risk → 3Open solution →GEN-PGX-004HLA-B*57:01/*15:02/*58:01
240 samples → 16 risk → 6Open solution →and
128 samples → 19 → 8
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CYP2D6 SNV/CNV/hybrid, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to pharmacogenomic interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology
86 samples → 7 risk → 4
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define DPYD, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to pharmacogenomic interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Genomics & Editing research and development
112 samples → 9 risk → 3
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define TPMT + NUDT15, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to pharmacogenomic interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Drug
240 samples → 16 risk → 6
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define HLA-B*57:01/*15:02/*58:01, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to pharmacogenomic interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Drug.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
VCF/BED/Big Wig/FASTA/CSV/HTML
MethodsSpliceAI, Pangolin, VEP, IGV
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-SPL-001CFTR and
96 → 12 candidates → 6 minigeneOpen solution →GEN-SPL-002DMD
78/windows → 10 candidates → 5 RT-PCR/ASOOpen solution →GEN-SPL-003BRCA1/2
132 → 14 candidates → 6 RNA validationOpen solution →GEN-SPL-004SMN2 exon 7
44 windows → 8 candidates → 4 ASOOpen solution →Genomics & Editing research and development
96 → 12 candidates → 6 minigene
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CFTR and, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to splicing variant mechanism design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
DMD
78/windows → 10 candidates → 5 RT-PCR/ASO
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define DMD, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to splicing variant mechanism design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for DMD.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology
132 → 14 candidates → 6 RNA validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define BRCA1/2, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to splicing variant mechanism design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
SMA
44 windows → 8 candidates → 4 ASO
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SMN2 exon 7, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to splicing variant mechanism design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for SMA.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/TSV/BED/CSV/XLSX
MethodsCas-OFFinder, Prime Design, BE-Hive, CRISPResso2
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-EDT-001+ cells SNP
186 guide → 12 + 4 controls → 16 wellsOpen solution →GEN-EDT-002SNV
176 designs → 16 + 4 controlsOpen solution →GEN-EDT-003SNV/indel
240 pegRNA designs → 18 + 6 controlsOpen solution →GEN-EDT-00450–500 genes
24,000 guide → 4–6/+Open solution →validation
186 guide → 12 + 4 controls → 16 wells
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define + cells SNP, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to genome-editing design sets.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for validation.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Genomics & Editing research and development
176 designs → 16 + 4 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SNV, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to genome-editing design sets.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Genomics & Editing research and development
240 pegRNA designs → 18 + 6 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SNV/indel, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to genome-editing design sets.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Genomics & Editing research and development
24,000 guide → 4–6/+
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 50–500 genes, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to genome-editing design sets.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
BEDPE/TSV/FASTA/PDB/CSV/XLSX
MethodsArriba, STAR-Fusion, VEP, IGV, Boltz
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-FUS-001Lung Cancer Kinase Fusion
73 → 11 candidates → 5 validationOpen solution →GEN-FUS-002NTRK1-3/FGFR1-4
58 → 9 candidates → 4 validationOpen solution →GEN-FUS-003BCR-ABL1 isoforms
26 designs → 6 → 3 validationOpen solution →GEN-FUS-004EWSR1 partner fusions
44 → 8 candidates → 4 validationOpen solution →Lung Cancer panel
73 → 11 candidates → 5 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Lung Cancer Kinase Fusion, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to fusion breakpoint interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Lung Cancer panel.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
panel
58 → 9 candidates → 4 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define NTRK1-3/FGFR1-4, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to fusion breakpoint interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for panel.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology
26 designs → 6 → 3 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define BCR-ABL1 isoforms, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to fusion breakpoint interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Genomics & Editing research and development
44 → 8 candidates → 4 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define EWSR1 partner fusions, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to fusion breakpoint interpretation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Genomics & Editing research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
VCF/FASTA/CSV/Gen Bank/JSON/XLSX
MethodsNetMHCpan, NetMHCIIpan, MHCflurry, pVACtools
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
GEN-NEO-001paired tumor/normal WES + tumor RNA + HLA-I/II
388 somatic mutations → 26,118 peptide–HLA predictions → 34 neoantigens → 1 mRNAOpen solution →GEN-NEO-002patients/HLA and
1,240 candidates → 18 → 12 tetramerOpen solution →GEN-NEO-003KRAS/TP53/PIK3CA and related targets
3,600 –HLA vs. → 48 candidatesOpen solution →GEN-NEO-00413–25mer
2,180 → 20 candidates → 8 CD4Open solution →Personalized Cancer Vaccine
388 somatic mutations → 26,118 peptide–HLA predictions → 34 neoantigens → 1 mRNA
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusPublic-data case study
A research-use workflow connects paired tumor/normal sequencing, tumor expression, HLA-I/HLA-II presentation, immunogenicity, clonality, and manufacturability without collapsing them into a single opaque score.
Balance HLA-I/HLA-II coverage, mutation clonality, tumor expression, peptide diversity, manufacturability, and redundancy.
Optimize ordering and linkers to reduce junctional epitopes while retaining processing and payload stability.
Computed ranking is not immune-response validation. Candidate-specific tetramer, ELISpot, or T-cell assays remain required.
Define paired tumor/normal WES + tumor RNA + HLA-I/II, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to neoantigen portfolio and construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Personalized Cancer Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
TCR-T
1,240 candidates → 18 → 12 tetramer
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define patients/HLA and, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to neoantigen portfolio and construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for TCR-T.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Vaccine/TCR
3,600 –HLA vs. → 48 candidates
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define KRAS/TP53/PIK3CA and related targets, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to neoantigen portfolio and construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Vaccine/TCR.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Vaccine
2,180 → 20 candidates → 8 CD4
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 13–25mer, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to neoantigen portfolio and construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
h5ad/rds/h5mu/Zarr/Parquet/model weights
MethodsScanpy, Seurat, scVI, sc Arches, Cell Typist
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
SC-ATL-001NSCLC tumor microenvironment
1.2M cells → 42 states → 3/validationOpen solution →SC-ATL-002CRC Oncology
433,804 candidate cells → donor-aware reference model → customer mapping and validation subpopulationsOpen solution →SC-ATL-003HCC/iCCA
760k cells → 36 states → 3 validationOpen solution →SC-ATL-004RA synovium
420k cells → 31 states → 5Open solution →SC-ATL-005Crohn/UC
680k cells → 40 states → 4Open solution →Lung Cancer
1.2M cells → 42 states → 3/validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define NSCLC tumor microenvironment, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to disease reference atlases.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Lung Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Colorectal Cancer
433,804 candidate cells → donor-aware reference model → customer mapping and validation subpopulations
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusPublic-data case study
Public single-cell cohorts are harmonized without erasing donor structure. Customer cells are mapped with state probabilities, out-of-distribution flags, and an orthogonal marker plan.
Version donors, tissues, assays, diagnoses, and ontologies before integration.
State probabilities, nearest references, unknown-cell flags, and candidate validation markers.
Reference labels guide interpretation; they do not replace pathology or functional validation.
Define CRC Oncology, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to disease reference atlases.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Colorectal Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Liver Cancer
760k cells → 36 states → 3 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define HCC/iCCA, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to disease reference atlases.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Liver Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
420k cells → 31 states → 5
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define RA synovium, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to disease reference atlases.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
680k cells → 40 states → 4
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Crohn/UC, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to disease reference atlases.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CSV/Parquet/h5ad/JSON/HTML/XLSX
MethodsCELLxGENE, HPA, Scanpy, cellxgene
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
SC-SAF-001CLDN18.2
152 cells → 7 sentinel risks → 5 validationOpen solution →SC-SAF-002TROP2/TACSTD2
152 cells → 9 sentinel risks → 6 validationOpen solution →SC-SAF-003CD276/B7-H3
152 cells → 8 sentinel risks → 5 validationOpen solution →SC-SAF-004GPRC5D
152 cells → 6 sentinel risks → 5 validationOpen solution →SC-SAF-005DLL3
152 cells → 5 sentinel risks → 4 validationOpen solution →CAR-T/ADC
152 cells → 7 sentinel risks → 5 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CLDN18.2, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to normal-tissue target safety maps.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for CAR-T/ADC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC/TCE
152 cells → 9 sentinel risks → 6 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define TROP2/TACSTD2, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to normal-tissue target safety maps.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC/TCE.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC/CAR-T
152 cells → 8 sentinel risks → 5 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CD276/B7-H3, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to normal-tissue target safety maps.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC/CAR-T.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
152 cells → 6 sentinel risks → 5 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define GPRC5D, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to normal-tissue target safety maps.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
152 cells → 5 sentinel risks → 4 validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define DLL3, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to normal-tissue target safety maps.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for SCLC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CSV/Parquet/h5ad/DuckDB/HTML/XLSX
MethodsDep Map, Scanpy, DuckDB, decoupleR
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
SC-MOD-001KRAS mutant backgrounds
64 models → 4 models + 2 controlsOpen solution →SC-MOD-002EGFR L858R/T790M/C797S
52 models → 5 models + 2 controlsOpen solution →SC-MOD-003T/NK/myeloid models
46 models → 4 models + 3 controlsOpen solution →SC-MOD-004hepatocyte/organoid models
38 models → 4 models + 2 controlsOpen solution →KRAS
64 models → 4 models + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define KRAS mutant backgrounds, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cell-line and organoid selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for KRAS.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Lung Cancer
52 models → 5 models + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define EGFR L858R/T790M/C797S, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cell-line and organoid selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Lung Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
46 models → 4 models + 3 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define T/NK/myeloid models, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cell-line and organoid selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
38 models → 4 models + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define hepatocyte/organoid models, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cell-line and organoid selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CSV/RDS/Parquet/h5ad/HTML
MethodsBayes Prism, Insta Prism, Mu SiC, decoupleR
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
SC-DEC-001NSCLC FFPE/RNA-seq
46 → 9 → 4 validationdesignsOpen solution →SC-DEC-002breast cancer cohorts
44 → 8 → 4 validationdesignsOpen solution →SC-DEC-003IBD mucosa bulk
38 → 7 → 3 validationdesignsOpen solution →SC-DEC-004MASH liver bulk
35 → 6 → 3 validationdesignsOpen solution →Immunotherapy biomarker
46 → 9 → 4 validationdesigns
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define NSCLC FFPE/RNA-seq, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell to clinical cohort translation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy biomarker.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Breast Cancer
44 → 8 → 4 validationdesigns
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define breast cancer cohorts, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell to clinical cohort translation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Breast Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
38 → 7 → 3 validationdesigns
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define IBD mucosa bulk, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell to clinical cohort translation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
35 → 6 → 3 validationdesigns
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define MASH liver bulk, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell to clinical cohort translation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
h5ad/Parquet/HTML/IPYNB/model cards
MethodsscGPT, Geneformer, sc Foundation, scVI, scib
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
cells
4 models + 3 → 1
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define annotation task, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell foundation-model audit.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
4 models + 3 → 2
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define integration task, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell foundation-model audit.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
cells
4 models + 2 → 1
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define perturbation task, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell foundation-model audit.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
4 models + 3 → 1
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define rare-cell task, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-cell foundation-model audit.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
AIRR TSV/h5ad/Parquet/FASTA/CSV
Methodsscirpy, MiXCR, TCRdist3, Dandelion
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
SC-REP-001pre/post ICI scRNA+TCR
8,420 → 96 candidates → 18 TCROpen solution →SC-REP-002CAR-T longitudinal VDJ
3,600 → 42 → 12 markerOpen solution →SC-REP-003RA/SLE BCR
6,200 → 84 candidates → 16 BCROpen solution →SC-REP-004viral antigen + HLA
4,800 → 72 candidates → 20 TCROpen solution →Immunotherapy
8,420 → 96 candidates → 18 TCR
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define pre/post ICI scRNA+TCR, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to tcr/bcr clone selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
cells
3,600 → 42 → 12 marker
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CAR-T longitudinal VDJ, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to tcr/bcr clone selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Single-cell & Tissue research and development
6,200 → 84 candidates → 16 BCR
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define RA/SLE BCR, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to tcr/bcr clone selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Single-cell & Tissue research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and Vaccine
4,800 → 72 candidates → 20 TCR
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define viral antigen + HLA, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to tcr/bcr clone selection.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/TSV/Parquet/BED/CSV/XLSX
MethodsViennaRNA, Bowtie, BLAST, RNAduplex
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
NA-SIR-001PCSK9
2,146 windows → 84 high-activity candidates → 10 designsOpen solution →NA-SIR-002ANGPTL3
1,988 windows → 76 high-activity candidates → 10 designsOpen solution →NA-SIR-003LPA
2,420 windows → 92 high-activity candidates → 12 designsOpen solution →NA-SIR-004TTR
1,640 windows → 68 high-activity candidates → 8 designsOpen solution →NA-SIR-005HBV conserved regions
3,200 windows → 110 conserved candidates → 12 designsOpen solution →Nucleic Acid Therapeutics research and development
2,146 windows → 84 high-activity candidates → 10 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PCSK9, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to sirna portfolio design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
1,988 windows → 76 high-activity candidates → 10 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define ANGPTL3, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to sirna portfolio design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
2,420 windows → 92 high-activity candidates → 12 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define LPA, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to sirna portfolio design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
1,640 windows → 68 high-activity candidates → 8 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define TTR, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to sirna portfolio design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
3,200 windows → 110 conserved candidates → 12 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define HBV conserved regions, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to sirna portfolio design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
HELM/FASTA/TSV/BED/CSV/XLSX
MethodsViennaRNA, RNAplfold, Bowtie, SpliceAI
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
NA-ASO-001SOD1
842 windows → 42 feasible ASOs → 10 designsOpen solution →NA-ASO-002HTT SNP-linked windows
1,120 windows → 36 and related targets candidates → 10 designsOpen solution →NA-ASO-003SMN2 exon 7
628 windows → 38 feasible ASOs → 10 + 4 controlsOpen solution →NA-ASO-004DMD selected exons
760 windows → 44 feasible ASOs → 12 designsOpen solution →NA-ASO-005MAPT isoforms
920 windows → 40 candidates → 10 designsOpen solution →842 windows → 42 feasible ASOs → 10 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SOD1, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aso gapmer and splice design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ALS.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Huntington
1,120 windows → 36 and related targets candidates → 10 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define HTT SNP-linked windows, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aso gapmer and splice design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Huntington.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
SMA
628 windows → 38 feasible ASOs → 10 + 4 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define SMN2 exon 7, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aso gapmer and splice design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for SMA.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
DMD
760 windows → 44 feasible ASOs → 12 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define DMD selected exons, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aso gapmer and splice design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for DMD.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Neuro
920 windows → 40 candidates → 10 designs
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define MAPT isoforms, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aso gapmer and splice design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Neuro.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
Gen Bank/FASTA/CSV/JSON/structure files/XLSX
MethodsViennaRNA, Linear Design, DNA Chisel, Biopython
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
NA-MRN-001viral/tumor antigen ORF
240 constructs → 12 Pareto constructs →/Open solution →NA-MRN-002secreted therapeutic protein
216 constructs → 10 constructs →/Open solution →NA-MRN-003membrane antigen/receptor
192 constructs → 10 constructs → surfacesOpen solution →NA-MRN-004Cas9/base editor ORF
264 constructs → 12 constructs →/Open solution →Vaccine
240 constructs → 12 Pareto constructs →/
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define viral/tumor antigen ORF, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to mrna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
216 constructs → 10 constructs →/
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define secreted therapeutic protein, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to mrna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
cells
192 constructs → 10 constructs → surfaces
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define membrane antigen/receptor, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to mrna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for cells.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Delivery
264 constructs → 12 constructs →/
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Cas9/base editor ORF, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to mrna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Delivery.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
Gen Bank/FASTA/CSV/HTML/XLSX
MethodsViennaRNA, Linear Fold, Biopython
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
NA-CIR-001vaccine antigen ORF
96 designs → 10 circRNA + 2 controlsOpen solution →NA-CIR-002cytokine ORF
88 designs → 10 circRNA + 2 controlsOpen solution →NA-CIR-003intracellular protein ORF
104 designs → 12 circRNA + 2 controlsOpen solution →NA-CIR-004luciferase/GFP
72 designs → 8 circRNA + 4 controlsOpen solution →Vaccine
96 designs → 10 circRNA + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define vaccine antigen ORF, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to circular rna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Vaccine.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Immunotherapy
88 designs → 10 circRNA + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define cytokine ORF, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to circular rna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
104 designs → 12 circRNA + 2 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define intracellular protein ORF, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to circular rna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Nucleic Acid Therapeutics research and development
72 designs → 8 circRNA + 4 controls
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define luciferase/GFP, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to circular rna construct design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Nucleic Acid Therapeutics research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
FASTA/CSV/PDB/SDF/HTML
MethodsViennaRNA, Boltz, Biopython, PyMOL
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
NA-APT-001PD-L1 extracellular domain
12,000 candidates → 480 structures seed → 12Open solution →NA-APT-002VEGF-A
10,000 candidates → 420 seed → 10Open solution →NA-APT-003thrombin exosites
8,000 candidates → 360 seed → 9Open solution →NA-APT-004EpCAM extracellular domain
11,000 candidates → 450 seed → 11Open solution →Diagnostics
12,000 candidates → 480 structures seed → 12
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PD-L1 extracellular domain, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aptamer seed-pool design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Diagnostics.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Diagnostics
10,000 candidates → 420 seed → 10
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define VEGF-A, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aptamer seed-pool design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Diagnostics.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Sensor
8,000 candidates → 360 seed → 9
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define thrombin exosites, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aptamer seed-pool design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Sensor.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology Diagnostics
11,000 candidates → 450 seed → 11
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define EpCAM extracellular domain, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to aptamer seed-pool design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology Diagnostics.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
OME-TIFF/SVS/DICOM-WSI/GeoJSON/CSV/Parquet/HTML
MethodsQu Path, Cellpose, Star Dist, MONAI, Open Slide, Squidpy
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-IHC-001CD8+ cells × Oncology
120 WSI → 2.8M cells → 3 → 1Open solution →IMG-IHC-002PD-L1 IHC × Oncologycells/cells
180 WSI → 12 → cases TPS/CPS +Open solution →IMG-IHC-003HER2 IHC × regions
96 WSI → 640 regions → 4 → 24Open solution →IMG-IHC-004CD8/CD4/FOXP3/CD68/PanCK
72 slides → 11 cells → 8 neighborhoods → 5 validation markerOpen solution →and
120 WSI → 2.8M cells → 3 → 1
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CD8+ cells × Oncology, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to ihc and multiplex pathology quantification.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Immunotherapy
180 WSI → 12 → cases TPS/CPS +
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define PD-L1 IHC × Oncologycells/cells, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to ihc and multiplex pathology quantification.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
96 WSI → 640 regions → 4 → 24
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define HER2 IHC × regions, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to ihc and multiplex pathology quantification.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Oncology
72 slides → 11 cells → 8 neighborhoods → 5 validation marker
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CD8/CD4/FOXP3/CD68/PanCK, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to ihc and multiplex pathology quantification.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
h5ad/Zarr/OME-TIFF/GeoJSON/CSV/Parquet/HTML
MethodsScanpy, Squidpy, cell2location, Tangram, Giotto, Seurat
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-SPX-001CRC tumor/adjacent Visium + scRNA reference
18 slides → 14 states → 6 → 10-marker validationOpen solution →IMG-SPX-002breast tumor spatial RNA + H&E + IHC
24 slides → 9 spatial domains → 4 → 8-marker panelOpen solution →IMG-SPX-003fibrotic liver zonation + stellate/macrophage states
20 slides → 12 states → 5 neighborhoods → 6Open solution →IMG-SPX-004brain spatial transcriptomics + glial reference
16 regions → 10 states → 4 lesionsneighborhoods → 8 validation markerOpen solution →Colorectal Cancer
18 slides → 14 states → 6 → 10-marker validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CRC tumor/adjacent Visium + scRNA reference, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to spatial transcriptomic states and niches.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Colorectal Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ICI
24 slides → 9 spatial domains → 4 → 8-marker panel
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define breast tumor spatial RNA + H&E + IHC, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to spatial transcriptomic states and niches.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ICI.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
20 slides → 12 states → 5 neighborhoods → 6
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define fibrotic liver zonation + stellate/macrophage states, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to spatial transcriptomic states and niches.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Neuro and
16 regions → 10 states → 4 lesionsneighborhoods → 8 validation marker
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define brain spatial transcriptomics + glial reference, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to spatial transcriptomic states and niches.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Neuro and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
SVS/OME-TIFF/GeoJSON/Parquet/ONNX/HTML
MethodsOpen Slide, timm, MONAI, UNI/CONCH, scikit-learn
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-HST-001breast/NSCLC H&E + immune labels
480 WSI → 42 candidates → 6 robust features → 1 modelsOpen solution →IMG-HST-002CRC H&E + MSI status
1,200 WSI → → ROI +Open solution →IMG-HST-003liver biopsy H&E/trichrome
320 WSI → 7 structures → +Open solution →IMG-HST-004resection H&E pre/post therapy
210 WSI → Oncology//→ casesOpen solution →Immunotherapy
480 WSI → 42 candidates → 6 robust features → 1 models
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define breast/NSCLC H&E + immune labels, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to h&e morphology and weakly supervised models.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
1,200 WSI → → ROI +
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CRC H&E + MSI status, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to h&e morphology and weakly supervised models.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
NASH
320 WSI → 7 structures → +
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define liver biopsy H&E/trichrome, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to h&e morphology and weakly supervised models.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for NASH.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
210 WSI → Oncology//→ cases
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define resection H&E pre/post therapy, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to h&e morphology and weakly supervised models.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
DICOM/NIfTI/SEG/CSV/Parquet/ONNX/HTML
Methodspydicom, SimpleITK, MONAI, Py Radiomics, nnU-Net, scikit-learn
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-RAD-001DCE-MRI × CD8 IHC/TIL/RNA-seq
182 → 91 → AUC 0.567/0.713 → validationOpen solution →IMG-RAD-002CT × PD-L1/CD8/RNA immune signature
620 → 84 robust features → 1 modelsOpen solution →IMG-RAD-003multiparametric MRI × fibrosis/spatial transcriptomics
240 → 5 → + ROIOpen solution →IMG-RAD-004multisequence MRI × IDH/immune microenvironment
410 → QC →/models +Open solution →Breast Cancer
182 → 91 → AUC 0.567/0.713 → validation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusReal-data feasibility and model-audit case
The published 182-case DCE-MRI design was audited and then rerun on 91 real multicenter MRI cases with expert segmentations and paired RNA evidence. The workflow was executable, but the locked-test evidence did not support clinical-grade prediction.
DICOM ingestion, segmentation audit, feature lineage, leakage-free train/test evaluation, and RNA label checks.
AUC 0.567 with wide uncertainty and permutation p=0.18 did not clear the predeclared evidence gate.
Prioritize trusted labels, larger center-diverse cohorts, and frozen external validation before adding model complexity.
Define DCE-MRI × CD8 IHC/TIL/RNA-seq, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to imaging-to-microenvironment prediction.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Breast Cancer.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Immunotherapy
620 → 84 robust features → 1 models
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define CT × PD-L1/CD8/RNA immune signature, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to imaging-to-microenvironment prediction.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Drug
240 → 5 → + ROI
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define multiparametric MRI × fibrosis/spatial transcriptomics, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to imaging-to-microenvironment prediction.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Drug.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Neuro Oncology
410 → QC →/models +
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define multisequence MRI × IDH/immune microenvironment, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to imaging-to-microenvironment prediction.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Neuro Oncology.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
DICOM/NIfTI/SEG/CSV/Parquet/HTML
MethodsSimpleITK, MONAI, Py Radiomics, lifelines, scikit-learn
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-RSP-001baseline/early-treatment DCE-MRI × pCR/RCB
260 → 3 → 8 delta → riskmodelsOpen solution →IMG-RSP-002serial CT × lesion response × immune outcomes
380 patients/1,420 lesions → 5 → patientsOpen solution →IMG-RSP-003serial CT/MRI × lesion-level response
210 patients → lesions vs. → 4 → casesOpen solution →IMG-RSP-004paired biopsy/SHG/MRI
160 vs.samples → 6 →Open solution →Bioimaging & Spatial Biology research and development
260 → 3 → 8 delta → riskmodels
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define baseline/early-treatment DCE-MRI × pCR/RCB, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to longitudinal imaging and treatment response.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Immunotherapy
380 patients/1,420 lesions → 5 → patients
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define serial CT × lesion response × immune outcomes, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to longitudinal imaging and treatment response.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Immunotherapy.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
ADC
210 patients → lesions vs. → 4 → cases
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define serial CT/MRI × lesion-level response, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to longitudinal imaging and treatment response.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ADC.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
160 vs.samples → 6 →
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define paired biopsy/SHG/MRI, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to longitudinal imaging and treatment response.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
OME-TIFF/DICOM/NIfTI/GeoJSON/Zarr/Parquet/HTML
MethodsANTs, Elastix, SimpleITK, Valis, Squidpy, MONAI
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
IMG-REG-001serial sections/same-slide multimodal tissue
12 samples → 3 → → ROIOpen solution →IMG-REG-002resection specimen × ex vivo/in vivo MRI
36 → → – → regionsOpen solution →IMG-REG-003IMC/CODEX × scRNA reference
2.4M cells → 16 states → neighborhoods + OODOpen solution →IMG-REG-004spatial RNA × phospho-IHC × morphology
18 slides → regions → 6 ROI → validation panelOpen solution →Bioimaging & Spatial Biology research and development
12 samples → 3 → → ROI
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define serial sections/same-slide multimodal tissue, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cross-modal registration and label transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
36 → → – → regions
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define resection specimen × ex vivo/in vivo MRI, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cross-modal registration and label transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
2.4M cells → 16 states → neighborhoods + OOD
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define IMC/CODEX × scRNA reference, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cross-modal registration and label transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Bioimaging & Spatial Biology research and development
18 slides → regions → 6 ROI → validation panel
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define spatial RNA × phospho-IHC × morphology, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to cross-modal registration and label transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Bioimaging & Spatial Biology research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
OER/ORR Catalysis
1,240 × → 380 surfaces → 22 → 3 to synthesize Catalysis
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define candidates +, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to catalyst adsorption screening.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for OER/ORR Catalysis.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
AI-guided Materials R&D research and development
860 sites → 190 relaxations → 14 Selectivitycandidates → 2 formulations
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define sites, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to catalyst adsorption screening.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for AI-guided Materials R&D research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Catalysis
5,000 → 640 → 30 |ΔG_H|<0.1 eV → 5 to test
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to volcano maps and reaction barriers.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Catalysis.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Catalysis
220 surfaces → 48 → 6 → 2 candidates
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define surfaces, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to volcano maps and reaction barriers.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Catalysis.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
ORR Catalysis
135 configurations → 41 → 7 → 3 synthesis targets
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define 27 ×, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to single-atom and doped catalysts.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for ORR Catalysis.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
AI-guided Materials R&D research and development
96 → 40 stable phases → 8 → 2 to synthesize
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to electrode intercalation voltage.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for AI-guided Materials R&D research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Liquid Electrolyte
360 → 120 relaxations → 12 → 3 formulations
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define × designs, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to electrolyte stability window and solvation.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Liquid Electrolyte.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Solid-state Battery
44 structures → 18 → 4 candidates → 1
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define candidatesstructures +, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to solid-electrolyte ion migration.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Solid-state Battery.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Drugand
3 → FMO/IP → PCET(pH 7) →
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusReproduced computational demonstration
This demonstration uses reproducible structure relaxation and electronic-structure descriptors to establish a relative ranking and a testable mechanism. Absolute energies or affinities are not presented as experimental truth.
Converge candidate structures, identify stable configurations, and expose the descriptors that drive the ranking.
3 → FMO/IP → PCET(pH 7) →
Final performance requires project-specific synthesis, electrochemical, surface, binding, or release validation.
Define SMILES + pH +, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to redox potentials and pcet.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Drugand.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
AI-guided Materials R&D research and development
Materials× → ΔEads/Δφ → selective pairs → formulations
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Materials ×, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to recognition materials and array deconvolution.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for AI-guided Materials R&D research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Neuro and
3 → PCET → → electrode-modification recommendation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusReproduced computational demonstration
This demonstration uses reproducible structure relaxation and electronic-structure descriptors to establish a relative ranking and a testable mechanism. Absolute energies or affinities are not presented as experimental truth.
Converge candidate structures, identify stable configurations, and expose the descriptors that drive the ranking.
3 → PCET → → electrode-modification recommendation
Final performance requires project-specific synthesis, electrochemical, surface, binding, or release validation.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to interferent separation design.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Neuro and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
FF-PAR-001Project-defined target and comparator set
N → QM →/→ multi-engine formatsOpen solution →FF-PAR-002Project-defined target and comparator set
12 → → → 5Open solution →FF-PAR-003+ surfaces
configurations → → parameterization → MDOpen solution →and
N → QM →/→ multi-engine formats
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to materials and interface force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
AI-guided Materials R&D research and development
12 → → → 5
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to materials and interface force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for AI-guided Materials R&D research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
and
configurations → → parameterization → MD
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define + surfaces, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to materials and interface force-field parameters.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
parameterization
Project-specific candidate funnel and validation package
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to torsion and conformer reference data.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for parameterization.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
AI-guided Materials R&D research and development
4 configurations → 4 UMA relaxations → N-down → mechanism report
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusReproduced computational demonstration
This demonstration uses reproducible structure relaxation and electronic-structure descriptors to establish a relative ranking and a testable mechanism. Absolute energies or affinities are not presented as experimental truth.
Converge candidate structures, identify stable configurations, and expose the descriptors that drive the ranking.
4 configurations → 4 UMA relaxations → N-down → mechanism report
Final performance requires project-specific synthesis, electrochemical, surface, binding, or release validation.
Define candidates, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to corrosion-inhibitor adsorption screening.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for AI-guided Materials R&D research and development.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
and
2 → 2 relaxations → ΔGbind → p
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusReproduced computational demonstration
This demonstration uses reproducible structure relaxation and electronic-structure descriptors to establish a relative ranking and a testable mechanism. Absolute energies or affinities are not presented as experimental truth.
Converge candidate structures, identify stable configurations, and expose the descriptors that drive the ranking.
2 → 2 relaxations → ΔGbind → p
Final performance requires project-specific synthesis, electrochemical, surface, binding, or release validation.
Define Drug ×, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to interface binding and charge transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
and
→ relaxations →/→ formulations
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to coatings, passivation, and antifouling.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
and Materials
→ FMO → → candidates
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to frontier-orbital and reactivity fingerprints.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and Materials.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
and
designs → relaxations/→ ΔG/Ka → Selectivity
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define × designs, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to host–guest and cluster binding.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
structures
→ ρ → per-atom →
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to difference density and charge transfer.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for structures.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
and
N wells Materials → adsorption sites → adsorption-energy window → candidates
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define wells Materialsstructures, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to porous-material adsorption screening.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for and.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
Drugpolymorphs
candidatespolymorphs → → stability ranking → crystallization recommendation
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define candidatespolymorphs, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to molecular-crystal polymorph ranking.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for Drugpolymorphs.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
Designed to answer one actionable R&D question: which candidates, controls, and validation experiments should advance together?
CIF/POSCAR/XYZ/SDF/JSON/CSV/Parquet/HTML/scripts
Methodsfairchem UMA, ASE, PySCF, Quantum ESPRESSO, pymatgen
EngagementProject-scoped quotation based on data readiness and assay capacity.
Lock the input, endpoint, controls, and exclusions
Generate a traceable candidate space
Calibrate orthogonal evidence and uncertainty
Select a diverse set under experimental constraints
Deliver assay-ready files and a data-return schema
New Materials Discovery
→ formation energy → distance to hull → candidates
Decision endpointA capacity-matched candidate set, controls, validation matrix, and auditable evidence package.
Evidence statusIllustrative planning example
The displayed candidate counts illustrate the operating scale and expected decision funnel. They are replaced by versioned customer data, explicit assay controls, and prespecified acceptance gates at project start.
Define Project-defined target and comparator set, success metrics, controls, data versions, and hard exclusions.
versioned project manifestGenerate a traceable candidate space appropriate to formation energy and phase stability.
candidate-space file and provenanceScore orthogonal evidence streams separately; preserve uncertainty, disagreement, and applicability limits.
evidence matrix with uncertaintyApply predeclared quality gates, leakage checks, robustness tests, and benchmark comparisons.
decision gate and exclusion logSelect a diverse, capacity-matched set for New Materials Discovery.
ranked experimental packageReturn raw measurements, QC flags, controls, batches, and failures in the supplied schema.
assay-ready data-return templateRetrain or recalibrate only after assay QC; propose the next experiment on a Pareto basis.
updated recommendation and next-round designRanked candidates, controls, sequence/structure/image identifiers, and selection rationale.
Separate evidence channels, uncertainty, applicability domain, exclusions, and version lineage.
Plate map or sample/ROI matrix, assay metadata, replicates, randomization, and QC rules.
Raw signal, normalized endpoint, batch, failure reason, and analysis-ready tables for the next round.
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