Atlas Baseline
Why this matters
A reference you build on.
You inherit your genome once.
Sequencing it gives you a permanent reference — a living dataset that becomes more valuable as science evolves.
AI is the right interpretation layer.
Variant-by-variant analysis against ClinVar, PharmGKB, and current literature. Not a template report — your specific mutations, investigated.
Your physician closes the loop.
High-impact findings are structured for clinical review. You do not interpret alone.
How it works
Three steps to your interpreted genome.

Order and complete intake.
Brief health questionnaire. Optional consultation with our medical geneticist in Germany.

At-home sample collection.
Saliva collection kit ships to your door. Painless, two-minute collection, prepaid return shipping.

Receive your interpreted genome.
Full raw data (VCF + FASTQ), structured findings report, clinician-readable summary. Delivered in 4–6 weeks.
What you get
Everything included.
Pricing
One price. Everything included.
One-time. Includes sequencing, AI interpretation, report, and full raw data.
Clinical context
Grounded in clinical infrastructure.
Atlas Baseline is processed through accredited laboratory partners. Reporting frameworks are developed in consultation with practicing physicians.

