aimosti

Compared

Five services that read the file you own, and where each one wins

If you already hold a DNA file, you have choices, and some of them are cheaper or broader than this one. These pages say so. Each compares Aimosti with one other service, read from that service's own pages on a stated day, and leads with what the other service does better before it gets to what a 30x genome makes possible here.

  • $25PrometheaseThe cheapest literature match there is, and the fastest. Wins on price and on the size of SNPedia. Does not grade, attribute or refuse.
  • LOCALGenetic LifehacksReads your chip file inside your own browser and never receives it. Wins on custody outright. Array files only; a genome must be converted down to one first.
  • 1500+SelfDecodeThe broadest consumer report set, with lab-result integration and an AI coach. Wins on breadth. Imputes, and says so; no reads, no copy number.
  • $64Gene2RxA 111-medication pharmacogenetics report from a whole-genome VCF for $64. Wins on VCF-only pharmacogenomics per dollar. Its own guide says copy number needs raw alignment files.
  • ANYSequencing.comTakes every raw format, stores it free, and screens sixteen thousand conditions at the top tier. Wins on format breadth and storage. Marketplace, subscription, and an AI that sends raw data to OpenAI.

How these pages are written

Every sentence about another service comes from that service's own public pages, and each page states the day it was read. Where a rival's own pages disagree with each other, we say which one we quoted. We concede the categories the other service wins, because a reader who already holds a file can check, and a comparison that only ever finds for its author is not worth reading. None of this is a review; it is a description you can verify.

What this service is, in one paragraph, so the comparisons have something to compare against: a one-time re-analysis of a file you already own, from €49 for a chip export and €89 for a whole genome, with an optional €109 pharmacogenomic panel read from your aligned reads. A fixed, named panel, listed before you pay; every finding attributed to a pinned source; processed and stored in Finland and deleted after analysis by default; and a report that says where it looked and declines where the file cannot answer. No imputation and no chat.