Clinical genomics
in minutes,
not days
Transform raw genomic data into expert-level clinical narratives with AI that thinks like a molecular pathologist. Automate the cognitive heavy lifting while keeping clinicians in control.
End-to-end cognitive automation
for clinical genomics
Unlike legacy platforms that act as digital filing cabinets, GenomeX is an AI-native clinical reasoning agent that automates the most cognitively demanding aspects of genomic interpretation.
AI Clinical Reasoning
Our agent doesn't just pattern match—it applies clinical reasoning frameworks used by expert molecular pathologists to interpret variants in context.
Minutes, Not Days
Transform a complex genomic case from raw data to complete clinical narrative in under 15 minutes. What used to take 2-3 days now happens before your next meeting.
Pathologist Control
Every interpretation is presented with full evidence chains and confidence scores. Pathologists review, edit, and approve—the AI augments, never replaces.
Clinical Narratives
Generate publication-quality reports that communicate complex genomic findings clearly to oncologists, genetic counselors, and patients.
Evidence Traceability
Every conclusion links back to primary literature, clinical databases, and ACMG/AMP guidelines. Full audit trail for every interpretation.
LIS Integration
Seamlessly connects with your existing laboratory information system. Fits into your workflow without disruption or re-training.
From raw data to clinical insight
Data Ingestion
Upload VCF, BAM, or raw sequencing files. Our pipeline handles QC, annotation, and normalization automatically.
HIPAA-compliant, encrypted transferVariant Analysis
AI-powered variant calling and classification using integrated databases including ClinVar, gnomAD, and COSMIC.
Real-time database syncClinical Reasoning
Our reasoning engine applies ACMG/AMP guidelines, literature evidence, and clinical context to generate interpretations.
Explainable decision logicVariant Classification
Each variant receives a classification—Pathogenic, Likely Pathogenic, VUS, Likely Benign, or Benign—with confidence scores.
Evidence-linked classificationsReport Generation
Generate comprehensive clinical narratives ready for pathologist review, complete with actionable recommendations.
Customizable templatesPathologist Review
You review, modify if needed, and sign off. Every edit is tracked. Your clinical authority is preserved.
Full audit trailValidated against the
gold standard
We don't ask you to trust AI blindly. Our platform is rigorously validated against expert pathologist consensus and published clinical databases.
Agreement with gold-standard pathologist interpretations across 2,500+ validated cases
Correct ACMG classification of variants compared to expert panel consensus
Validated performance across solid tumors, hematological malignancies, and hereditary syndromes
From data upload to complete clinical narrative, with full evidence documentation
Validation Studies & Publications
Multi-site Validation Study
Prospective validation across 5 academic medical centers with 1,200 consecutive cases
CAP Proficiency Assessment
Blinded evaluation using College of American Pathologists survey samples
Hereditary Cancer Panel Study
Head-to-head comparison with leading commercial laboratories on 847 BRCA1/2 cases
Regulatory & Compliance Ready
GenomeX is designed with healthcare compliance at its core. Our platform maintains SOC 2 Type II certification, HIPAA compliance, and follows FDA guidance for clinical decision support software.
Trusted by leading
pathology teams
Hear from molecular pathologists and lab directors who are transforming their clinical genomics workflows with GenomeX.
“GenomeX has fundamentally changed how we approach complex oncology cases. What used to take our team 3 days now takes under 20 minutes, with the same level of clinical rigor.”
“The evidence traceability is exceptional. Every interpretation links back to primary literature and clinical databases. This gives us confidence to sign out reports faster.”
“As a lab director, I was skeptical of AI in clinical genomics. GenomeX changed my mind. The human-in-the-loop design means pathologists stay in control while dramatically reducing cognitive load.”
Partnering with leading institutions
Ready to transform your
genomics workflow?
Join leading molecular pathology labs in our design partner program. Get early access, shape product development, and be first to deploy when we launch in 2026.