Built for Every Stakeholder

Eliminate the 14-day diagnostic lag in NICU, oncology, and rare disease. SMART on FHIR integration with Epic and Cerner delivers court-defensible reports with full PMID traceability.

Real-time prescription interception at point of fill. Coverage spans CYP2D6, CYP2C19, DPYD, SLCO1B1 and all 608+ FDA drug-gene mandates.

Population pharmacogenomics stratification with automated prior authorization backed by genomic evidence. Reduce preventable ADR hospitalizations across your covered lives.

PROTEUS simulates up to 5,000 generations of genomic evolution for trial design and resistance prediction. 1,000-generation benchmarks in 130 seconds, scaling to 5,000-generation extended discovery runs. Identify PGx stratification requirements and accelerate rare disease discovery 40–60%. The Study Dossier production layer turns that evidence into research-grade artifacts with cryptographic provenance and validator-gated export.