For Providers

Built for Every Stakeholder

Clinical genomics infrastructure that integrates with your existing workflows. Health systems, pharmacies, health plans, and pharma R&D.

Health Systems

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.

Complete genome resolution in under 30 seconds

FHIR-native export to existing EHR workflows

ACMG SF v3.2 secondary findings coverage

Estimated $10M+ annual savings per network

Pharmacies & PBMs (COMING SOON)

Real-time prescription interception at point of fill. Coverage spans CYP2D6, CYP2C19, DPYD, SLCO1B1 and all 362+ FDA drug-gene mandates.

Point-of-fill pharmacogenomic screening

Star allele dosing recommendations

Adverse drug reaction liability reduction

Integration with pharmacy management systems

Health Plans

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

Population-level PGx stratification

Automated prior authorization with genomic evidence

Preventable ADR hospitalization reduction

1.2M clinical rules applied per member

Pharma R&D

PROTEUS simulates 1,000 generations of genomic evolution for trial design and resistance prediction. Identify PGx stratification requirements and accelerate rare disease discovery 40–60%.

$10K–$500K per simulation vs $800M Phase III failure

Drug resistance pattern prediction

PGx stratification for trial design

40–60% rare disease discovery acceleration

Ready to Transform Your Genomics Workflow?

Give us 60 minutes and we'll show you something nobody else has.

Schedule a Demo