aimosti

MyHeritage raw data analysis

Re-read your MyHeritage DNA file — without it leaving the EU

MyHeritage gave you ethnicity estimates and relatives. The same raw genotype file also carries clinical and pharmacogenomic variants worth reading properly. Re-analyse the file you already own against current evidence — processed and stored in Finland, attributed to every source.

Re-analyse my MyHeritage file · €79 See a sample report first

€79 one-time · the report is yours to keep · processed in the EU, never sold.

A European service for a file you already own

Aimosti is based in Finland and keeps your data inside the EU — which matters if data sovereignty is part of why you tested with MyHeritage in the first place. We don't sequence you again; we re-interpret the raw genotype file MyHeritage produced, against today's ClinVar, ACMG and CPIC, and return a report you keep. Whatever health features exist in your MyHeritage account, the raw file holds variants that a re-analysis can surface and attribute.

How to download your MyHeritage DNA raw data

  1. Sign in at MyHeritage and open the DNA menu, then Manage DNA kits.
  2. For your kit, open its options and choose Download (MyHeritage walks you through a short consent step).
  3. Confirm; MyHeritage emails you a secure download link.
  4. Follow the link to get the raw file (a zipped .csv/.txt). That archive is what we re-analyse — store it somewhere private.

What a MyHeritage chip can — and can't — show

MyHeritage genotyping arrays read a fixed panel of positions; the exact set has changed across chip versions, so coverage of specific pharmacogenomic and carrier variants varies from file to file. We handle whichever version you have, and stay honest about the limits:

  • We read your file's actual positions and attribute every finding to a primary source.
  • No-calls are shown as no-calls — we don't impute over positions the chip didn't read.
  • Structural variation isn't resolvable from array data — CYP2D6 copy-number is the classic example — so where a metabolizer status would be uncertain, we mark it indeterminate.

For coverage beyond any chip, a whole-genome re-analysis goes deeper — but the MyHeritage file is an honest, useful place to start.

Where your file lives

Processed and stored in Finland, never leaving the EU (GDPR Article 9). The raw upload is deleted after analysis by default, and there's no genome vault to be sold — see the security architecture. For the wider context on why "who holds your DNA" became the question everyone's asking, read the 23andMe bankruptcy explainer.

Aimosti performs a bioinformatic re-analysis of data you already own. We never take a sample, sequence, test, or diagnose. Every finding is a literature match to confirm with a clinician, not a diagnosis.

Why not the €23 option?

Promethease and Genetic Genie read the same public databases we do. The difference is time. They hand you a report frozen on the day you run it, built from the few thousand positions a genotyping chip happens to type. We read your whole genome where you have it, attribute every finding to the guideline it came from, and re-read your file as those guidelines change. You buy the careful version once, and it stays current. You keep it either way.

Named services are described from their public product pages; features change and we don't speak for them. Cheaper isn't the problem. What "frozen the day you ran it" costs you three years later is.

A one-time MyHeritage re-analysis is €79. The report is yours to keep.

See a sample report Re-analyse my MyHeritage data: €79

Other file types: 23andMe raw data · AncestryDNA raw data · Choosing a service that never holds your genome.