One careful re-analysis. Yours to keep.
Drop in the genetic file you already have. We detect whether it is a genotyping-chip export, whole-genome data, or aligned reads, then show you what your report will cover before you pay. We re-read it and attribute every finding to its source, so you can check where a result came from. Every report stays yours for good.
Choose your starting point
Not sure which file you have? Drop it in and we will tell you. Otherwise, pick below.
Most whole-genome reports on GRCh38 are ready 5–15 minutes after the upload finishes. A GRCh37 file is lifted to GRCh38 first, and a large gVCF on that build can take a couple of hours. Deep Read takes about half an hour once the reads are in.
Chip report
For 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, LivingDNA and similar genotyping-array raw-data exports. Everything your chip can call, fully attributed. Carrier status and the full clinical-findings panel need whole-genome data (WGS). MyHeritage kits sold since October 2025 may be sequenced rather than typed on an array, so check which file you have.
- Clinical findings your array covers
- Pharmacogenomics for the genes your chip typed and resolved
- Traits, ancestry and the Frontier module
- Polygenic scores and single-gene findings
- A one-page clinician hand-off, built from the same findings
- Plain-language explainers, save as PDF
Already on a chip report? Upgrade to the full WGS report for €20 any time. Chip plus upgrade comes to €39. The full report on its own is €39.
Full report (WGS)
Every module over your whole-genome file. Upload a gVCF for coverage-proven findings (a plain VCF also works). A one-time analysis, yours to keep.
- Clinical findings (ClinVar and ACMG SF)
- Carrier status and pharmacogenomics: 8 pharmacogenes from a plain VCF, 25 from a gVCF, each card stating how many defining positions your file examined
- Traits, ancestry, Frontier and the Fringe
- Polygenic risk scores, with your percentile against a reference population
- A one-page clinician hand-off, built from the same findings
- Pinned, attributed, reproducible sources
Full report + Deep Read
Deep Read works out to €60 here, vs €79 on its own. The full WGS report plus the Deep Read panel, prepaid together.
- Everything in the full report
- Deep Read: CYP2D6 copy number and star alleles, from your reads
- Per-gene callability, measured directly
- Two recurrent deletions called from depth; HLA-DQ typed
Add when you are ready
Deep Read
The answers only your aligned reads hold: the BAM or CRAM your sequencing provider gave you, on GRCh38 or GRCh37. A variant file cannot see a gene's copy number, cannot say how much of a gene it actually examined, and cannot type HLA. Deep Read reads all of that from the reads, resolves the full 29-target pharmacogene panel to CPIC star alleles on the way, and turns it into a one-page hand-off for your prescriber. It costs a little more than the full report because it reads tens of gigabytes of aligned data with lab-grade star-allele calling. Most people save by taking it in the bundle.
- CYP2D6 copy number and star alleles: the duplication a variant file cannot see
- Per-gene callability, measured directly from read depth
- Two recurrent deletions (TYROBP, CLN3) called from depth
- HLA-DQA1 and HLA-DQB1 typed from the reads, which is what a celiac rule-out needs
- G6PD read as a single copy where that is what you carry
- The full 29-target panel (CYP2C19, TPMT, DPYD, SLCO1B1 and more) and a one-page medication hand-off
- Reads processed, then deleted immediately
Why does this panel need aligned reads?
CYP2D6 is the clearest example. It governs how the body metabolises dozens of common drugs, from antidepressants to codeine, and its gene structure (duplications, deletions, pseudogene interference) means a variant file cannot see whether you carry one copy or three. Most of the rest of the panel can now be resolved from a gVCF inside the full report, so what stays with the reads is exactly what needs depth: copy number, how much of each gene was actually examined, the recurrent deletions, and HLA typing. Deep Read measures, gene by gene, the fraction of bases we could examine at read depth of 10× or more, turning "not found" into "examined, and not found".
Offered from your dashboard once your report is ready, so there is no large upload up front. Prepay it with the bundle to save €19.
Start with the full report · €39Re-analysis subscription
Your genome doesn't change. The science does. Keep any report live for €29/yr and we re-read your file as the science moves; your dashboard flags when new data is ready. Without it, your report stays the snapshot you bought.
- Silent re-matching of your variant file
- "What changed" updates as the science moves
- Only your normalised variants are kept
- You keep every report you have ever had. The subscription only adds new updates
- Cancel any time
Add it at any time, before or after your report. How updates work.
No hidden fees. No data resale (that is how the "free" services pay). One transparent price for a careful, attributed re-analysis you own.
What each file type can tell you
The same coverage table we show you before you pay. A number is how many items we examine in a module; a tick means included; a dash means that file type cannot deliver it.
| What you get | Chip | WGS | WGS + Deep Read |
|---|---|---|---|
| Clinical findings | 2 examined | 39 examined | 39 examined |
| Carrier status | Not available | 55 examined | 55 examined |
| Pharmacogenomics | 8 examined[1], see note 1 | 8 examined | 8 examined |
| Traits | 26 examined | 26 examined | 26 examined |
| Frontier | 38 examined | 38 examined | 38 examined |
| The Fringe | 20 examined | 20 examined | 20 examined |
| Archaic ancestry | 9 examined | 9 examined | 9 examined |
| Polygenic scores | 6 examined | 6 examined | 6 examined |
| Ancestry: maternal (mtDNA) | 11 examined | 11 examined | 11 examined |
| Ancestry: paternal (Y-DNA) | 14 examined[2], see note 2 | 14 examined | 14 examined |
| Ancestry composition | 30 examined | 30 examined | 30 examined |
| APOE risk allele (e4) | Included | Included | Included |
| Lp(a) level | Included | Included | Included |
| Hemochromatosis (HFE) variants | Included | Included | Included |
| ABO blood type | Not available | Included | Included |
| APOL1 risk variants | Included | Included | Included |
| Celiac HLA types (DQ2.5 / DQ8) | Included[3], see note 3 | Included | Included |
| Deep Read: 29-target PGx panel + callability | Not available | Not available | 29 examined |
| Recurrent deletion calls (from read depth) | Not available | Not available | 2 examined |
[1]Note 1: Array-dependent: only the genes whose defining SNPs your chip both typed and could resolve. DPYD needs a sequenced file.
[2]Note 2: Needs your export's genome build, which 23andMe and AncestryDNA files give us. MyHeritage and FamilyTreeDNA exports don't state it, so for those we report the paternal line as unreadable rather than guess at it.
[3]Note 3: Array-dependent: both marker positions must be on your chip and readable from it. When they are not, the result reads as not called rather than as a negative.
A number is how many items we examine; means included; a dash () means that file type can't deliver it. Counts are the most a file of that type can give you, not a promise for every file.
These are curated, reviewed panels, not a comprehensive genome-wide screen, and the absence of a finding is not a clean result. A chip only reports the specific variants it typed, so its counts are an upper bound; full clinical findings and carrier status need whole-genome data (WGS). Counts are version-stamped (2026-08-08) from the analysis registries. Polygenic scores are calibrated to broad ancestry groups and report your percentile against a reference population, not a personal probability of disease. Drop your file to see what yours covers.
Where Aimosti sits
| Service | Price | Updates | Input | Note |
|---|---|---|---|---|
| Genetic Genie | Free | Frozen | chip / VCF | Ad-supported, stale curation |
| Promethease | ~€23 | Frozen | chip / VCF | One-time SNPedia report, dense |
| SelfDecode | ~€92 / yr | Rented | chip (imputed) | Access stops when you stop paying |
| Aimosti | €39 once | Current & yours | whole-genome / chip | WGS-native (chip welcome), attributed, EU-sovereign |
Every other option hands you a one-time report frozen at the day you run it, or rents you ongoing access. Aimosti re-reads your file as the science moves, and the report stays yours. We charge more than the options above. That buys WGS-native depth, pinned curation you can re-check, and data that stays in the EU. And we never impute: where others fill in the genotypes a chip missed with a statistical guess, nothing in our pipeline invents a genotype. A no-call in your file reaches your report as a no-call.
One report. Yours to keep.
Read in Finland, attributed to the source, never sold.
See what your file covers