Clinical-Grade Genomics. Priced for Every Lab.
Affordable variant interpretation, AI-powered clinical reports, and modular genomics tools — built for clinical labs, academic centers, and genetic testing companies.
Everything You Need for Genomic Interpretation
A modular, cloud-native platform designed for clinical genomics workflows.
How It Works
From raw data to clinical report in four steps.
Upload Your Data
Upload VCF or FASTQ files with automated format validation and quality checks.
Annotate & Score
Variants annotated with ClinVar, gnomAD, CADD, SpliceAI and prioritized via HPO scoring.
Interpret & Classify
Interactive workbench for variant review with ACMG/AMP classification guidance.
Generate Report
AI-generated clinical reports with evidence citations and mandatory human review.
Simple, Transparent Pricing
Genomics interpretation shouldn't break the budget.
Pay Per Sample
Only pay for what you use. No seat licenses, no minimum commitments.
No Lock-In
Export your data anytime. Standard formats, open APIs, zero vendor lock-in.
Volume Discounts
Automated tiered pricing that scales with your throughput.
Early access labs receive special founding pricing.
Ready to Transform Your Genomics Workflow?
Join the next generation of clinical labs using Clarigenome for faster, more affordable genomic interpretation.