Aimosti The European alternative to Genomelink
SubmittedGenome re-analysis from Finland based on existing DNA data
About Aimosti
Aimosti is a service for re-analyzing existing DNA data that users upload themselves. Variants are matched against current clinical and research databases and presented with versioning. The provider emphasizes that this is not a medical test or diagnosis.
Highlights
- ✓ Analyzes existing genome or genotyping raw data, no test kit
- ✓ Modules for clinical findings, carrier status and pharmacogenomics
- ✓ Automatic re-analysis when the evidence changes
- ✓ Results with source attribution and versioning
- ✓ Raw data is deleted by default after the analysis
Why European?
- → Genetic data as a special category stays in Finland and the EU
- → Explicit and revocable consent under GDPR Article 9
- → Data is not sold or shared according to the provider
- → EU jurisdiction for highly sensitive health data
Pricing
Chip report from EUR 49 · whole-genome report EUR 89 (one-time) · update subscription EUR 29/year.
Frequently asked questions about Aimosti
What is Aimosti and what is it used for? +
Aimosti is a service from Aimosti Oy in Finland that re-analyzes existing DNA data. Users upload raw data they already own, for example from whole-genome sequencing or genotyping chips. Aimosti matches the variants against databases such as ClinVar, CPIC and the GWAS Catalog and shows what the current evidence says about a variant. No test kit is sold; the service works exclusively with data that already exists.
Does Aimosti run on European infrastructure? +
According to the provider, data is processed and stored in Finland and does not leave the EU, with encrypted transfer. A specific cloud provider is not named on the public pages. Aimosti processes genetic data as a special category under GDPR Article 9 and obtains explicit, revocable consent for this. Raw data is deleted by default after the analysis, and deletion on request is possible.
Is Aimosti a medical test? +
Aimosti explicitly states that it is not a medical test or diagnosis. The service restates the existing scientific evidence on variants and points users to confirm findings with medical professionals and a validated test. It does not replace medical advice or a clinical examination. The results are for information and are presented with sources and version status.
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Entry verified on 05.08.2026