INTERPRET. EXPLAIN. ORIGINS.
Genome Insights, Not Lab Work
Upload your genome, and we translate it into mutation insights, trait context, and a clear story of where you come from.
100%
Your data ownership
Health & ancestry
Focus areas
$15
Expert review upgrade
AES-256
Data security
Interpretation without lab work
We are a genome intelligence team, not a wet lab. Every insight starts with the digital data you already own.
- No sample kits, swabs, or hidden specimen processing.
- Encrypted upload or courier drive options for your completed genome files.
- Integrity checks confirm your files arrive untouched and ready for review.
Mutation insights you can act on
We focus on the variants that matter: health, wellness, and trait markers you care about.
- Variant curation surfaces pathogenic, likely pathogenic, and notable VOUS findings.
- Clear explanations and next-step suggestions for discussing results with your physician.
- Interactive variant graphs spotlight hotspots and highlight where action is recommended.
Origins mapped with context
We translate your genome into an origin narrative covering ancestral migration paths, haplogroups, and regional affinities.
- Mitochondrial and Y-chromosome haplogroup analysis where data allows.
- Regional breakdowns anchored in peer-reviewed population references.
- Story-driven summaries you can share with family or keep for your records.
Visual stories that make sense
We turn complex data into intuitive visuals so you can explore every insight at a glance.
- Dynamic ancestry graphs show maternal and paternal lineages side by side.
- Trait dashboards layer bar charts, heat maps, and timelines for fast comparisons.
- Word-map narratives surface the key themes and descriptors tied to your genome.
Everything stays under your control
You decide what we interpret, when we start, and how long your data remains with us.
- Analysis begins only after you approve the exact questions we answer.
- Isolated compute environments keep your genome separated from every other client.
- Request secure deletion or extended vaulting the moment you have what you need.
Frequently Asked Questions
Do you collect or process biological samples?
No. We are not a lab. We only work with the digital genome files you already have from sequencing providers.
What do I need to get started?
Upload your whole-genome or exome data in FASTQ, BAM/CRAM, or VCF format and select the insights you want: mutations, traits, and history.
Can you explain both mutations and ancestry?
Yes. We flag clinically relevant variants, translate trait impacts, and decode ancestry signals into an accessible origin story.
Ready for genome interpretation?
Share your data, choose your focus areas, and receive interactive graphs, dashboards, and word maps that bring your genome story to life.