Now accepting design partners for 2026

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.

98.7%
Concordance with gold standard
<15 min
Average report generation
Platform Capabilities

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.

Thinks like an expert

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.

95% time reduction

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.

Human-in-the-loop

Pathologist Control

Every interpretation is presented with full evidence chains and confidence scores. Pathologists review, edit, and approve—the AI augments, never replaces.

Clear communication

Clinical Narratives

Generate publication-quality reports that communicate complex genomic findings clearly to oncologists, genetic counselors, and patients.

Complete transparency

Evidence Traceability

Every conclusion links back to primary literature, clinical databases, and ACMG/AMP guidelines. Full audit trail for every interpretation.

Zero friction

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

01

Data Ingestion

Upload VCF, BAM, or raw sequencing files. Our pipeline handles QC, annotation, and normalization automatically.

HIPAA-compliant, encrypted transfer
02

Variant Analysis

AI-powered variant calling and classification using integrated databases including ClinVar, gnomAD, and COSMIC.

Real-time database sync
03

Clinical Reasoning

Our reasoning engine applies ACMG/AMP guidelines, literature evidence, and clinical context to generate interpretations.

Explainable decision logic
04

Variant Classification

Each variant receives a classification—Pathogenic, Likely Pathogenic, VUS, Likely Benign, or Benign—with confidence scores.

Evidence-linked classifications
05

Report Generation

Generate comprehensive clinical narratives ready for pathologist review, complete with actionable recommendations.

Customizable templates
06

Pathologist Review

You review, modify if needed, and sign off. Every edit is tracked. Your clinical authority is preserved.

Full audit trail
Clinical Evidence

Validated 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.

98.7%
Concordance Rate

Agreement with gold-standard pathologist interpretations across 2,500+ validated cases

99.2%
Classification Accuracy

Correct ACMG classification of variants compared to expert panel consensus

40+
Cancer Types

Validated performance across solid tumors, hematological malignancies, and hereditary syndromes

12 min
Median TAT

From data upload to complete clinical narrative, with full evidence documentation

Validation Studies & Publications

Completed 2024

Multi-site Validation Study

Prospective validation across 5 academic medical centers with 1,200 consecutive cases

98.3% concordance with institutional pathologist interpretations
Ongoing

CAP Proficiency Assessment

Blinded evaluation using College of American Pathologists survey samples

100% correct on all proficiency testing challenges
Published 2024

Hereditary Cancer Panel Study

Head-to-head comparison with leading commercial laboratories on 847 BRCA1/2 cases

99.1% concordance, 23% reduction in VUS rate

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.

HIPAA Compliant
SOC 2 Type II
CLIA Ready
From Our Partners

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.

Dr. Sarah Chen
Dr. Sarah Chen
Director of Molecular Pathology
Memorial Cancer Institute

The evidence traceability is exceptional. Every interpretation links back to primary literature and clinical databases. This gives us confidence to sign out reports faster.

Dr. Michael Torres
Dr. Michael Torres
Chief of Laboratory Medicine
University Medical Center

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.

Dr. Rebecca Okonkwo
Dr. Rebecca Okonkwo
Lab Director
Regional Health System

Partnering with leading institutions

Academic Medical Centers
Cancer Research Institutes
Reference Laboratories
Health Systems
Limited Design Partner Slots

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.

No commitment required
30-minute demo

Design Partner Benefits

Priority access before general availability
Direct input on product roadmap
Dedicated implementation support
Preferential launch pricing
Co-marketing opportunities
Early validation study participation
Design Partner Slots
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