Atlas Baseline.
Sequence your genome once. Read it for the rest of your life.
Atlas Baseline sequences your full genome at our Berlin lab and interprets it with a dedicated AI agent. Significant findings, pharmacogenomic insights, and follow-on recommendations — built to share with your physician.

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.
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.
Everything included.
- Clinical-grade 30x whole genome sequencing
- AI-powered variant interpretation (ClinVar, PharmGKB, literature)
- Full raw data: VCF + FASTQ files, yours forever
- Structured findings report (significant variants, pharmacogenomics, screening recommendations)
- Clinician-readable summary (PDF, shareable)
- Optional pre-test genetic consultation (Germany)
One price.
Everything included.
One-time. Includes sequencing, AI interpretation, report, and full raw data.
Grounded in clinical infrastructure.
Atlas Baseline is processed through accredited laboratory partners. Reporting frameworks are developed in consultation with practicing physicians.
- Charité — Universitätsmedizin BerlinResearch-adjacent development context
- University Hospital BonnClinical advisory framework
- Processed at Atlas Biolabs, BerlinLaboratory processing

Structured outputs designed for clinical review
Questions.
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