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:

1. 1
   Create your account

   One click with Google and this step is done: Google confirms your address, so there's no link to go and find. Email and password works too; we'll send a confirmation link. Your free preview opens once you've used it.

2. 2
   Set your consent

   Separate and revocable: one required permission to process your file, research use off by default, and a box to opt out of our occasional emails.

3. 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.

4. 4
   Read your report

   A dozen modules, every finding attributed to its source and yours to keep. Add the $49 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.