Pricing
Project-based pricing. Gate-ready deliverables.
Each tier is a fixed-fee engagement with ranked targets and evidence dossiers. Resistance mapping, proprietary cohort integration, and custom GNN training are quoted per scope.
Explorer
$75K
2 weeks delivery
Single indication, public multi-omics data, up to 500 genes evaluated
- Multi-omics integration
- Ranked target list (top 8)
- Druggability + safety scores
- Evidence summary per target
- Email support
Most popular
Professional
$175K
3 weeks delivery
Multi-omics + proprietary cohorts, knowledge-graph GNN, gate package
- Everything in Explorer
- Up to 15 priority targets with dossiers
- Competitive landscape briefs
- Portfolio gate presentation deck
- Validation roadmap
- Priority support
Enterprise
Custom
Flexible delivery
Multi-indication franchise, resistance mapping, custom knowledge graphs
- Everything in Professional
- Dedicated project lead
- Proprietary cohort integration
- Resistance pathway mapping
- Quarterly model refinement
- On-site scientist exchange
Add-ons: Resistance pathway mapping, proprietary cohort integration, investor diligence packages, and custom knowledge-graph model training are quoted separately.
Frequently asked questions
- How do you validate target rankings?
- Across closed engagements, 75 to 90 percent of Priority A targets were supported by independent clinical or genetic evidence at portfolio review. Rankings are calibrated against gate outcomes, not public benchmarks alone.
- What data formats do you accept?
- GWAS summary statistics, bulk and single-cell RNA-seq (FASTQ or count matrices), proteomics tables, and structured CSV gene lists. We integrate public repositories (GEO, Open Targets) and client proprietary cohorts under NDA.
- Can you reconcile with our internal target lists?
- Yes. We produce reconciliation reports showing which internal hits are upgraded, downgraded, or confirmed—with documented rationale for each change.
- What's included in an evidence dossier?
- Each dossier covers genetic evidence, expression context, pathway role, druggability score, safety tier, competitive landscape, evidence concordance tier, and recommended validation experiments.
- Do you sign IP and confidentiality agreements?
- Always. We sign a mutual NDA before any technical discussion. All generated analysis and dossiers belong to the client by default.
