Re-analyse the genome you already own
No new sample, no sequencing: you bring the data, we re-interpret it against current science. Here's the whole journey before you spend a cent:
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1
Create your account
Email and password, or continue with Google. About a minute, plus a confirmation link we'll email you. Checkout and upload stay closed until you open it.
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2
Set your consent
Separate and revocable: one required permission to process your file, everything else optional and off by default.
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3
Upload your genome
Your gVCF (preferred, it proves coverage) or plain VCF from Nebula, Dante, Sequencing.com or similar, or raw genotyping-array data from 23andMe, AncestryDNA, MyHeritage (whose newer kits are sequenced instead), FamilyTreeDNA or LivingDNA, straight to EU storage, encrypted in transit. The report is €39 one-time for a whole genome, or €19 from a chip file.
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4
Read your report
A dozen modules, every finding attributed to its source and yours to keep. Add the €79 Deep Read later for a read-level 29-target pharmacogenomic panel including CYP2D6, plus a per-gene report of how much of each gene your file actually covered.
Your data stays in the European Union (Finland), encrypted in transit, and is never sold. Delete any time.