aimosti

Compared · Genetic Lifehacks

Genetic Lifehacks never receives your file. That is a real advantage, and it has a cost.

Genetic Lifehacks reads a chip export inside your own browser and matches it to several hundred articles written by one person over a decade. On custody it wins outright. What it cannot read is a genome, and that is the whole difference.

Where Genetic Lifehacks wins

Custody. Its own pages say it plainly: "When you connect your file, it's read inside your own browser, on your own device. We never receive it, never see it, and never store it." Our free file check works the same way, but our report does not: the file is uploaded, analysed in Finland and deleted after analysis by default. For the core report tool, Genetic Lifehacks holds nothing, and no custodial service can match that claim. We do not try to.

Price for an ongoing read. Its membership page lists $11.99 a month, $49.99 a year, or $119 for life, and a professional tier at $179.99 a year. A year of membership costs less than a chip report here, and a lifetime costs about the same as a whole-genome report.

Depth of explanation. The homepage counts "over 420 in-depth genotype reports and 20 summary reports", written and curated by its founder. They are long, sourced and readable, and they cover nutrition and lifestyle ground our panel does not touch.

Where the two differ

Genetic LifehacksAimosti
Price$11.99/month · $49.99/year · $119 lifetime (its membership page)€49 chip · €89 whole genome · €109 reads panel, each one-time
What it reads23andMe, AncestryDNA, MyHeritage and similar array exports as .txt, .csv or .zip; "Whole-genome data (VCF or BAM files need conversion first)" (its compatibility page)Chip exports, VCF, gVCF, and BAM or CRAM for the reads panel, as delivered
Where the file goesNowhere: read in the browser and gone when the tab closes (its own words), for the report toolUploaded to Finland, analysed, deleted after analysis by default
What the report isYour genotypes shown inside topic articles, plus summary reportsFixed, named panels graded into three evidence tiers, each finding attributed to a pinned source version
PharmacogenomicsGenotypes inside articles; no star-allele or guideline claim on its pagesCPIC star alleles from a VCF; a 29-gene panel called from reads, CYP2D6 copy number included
Clinician hand-offPrintable summaries for members; client reports on the professional tierA one-page clinician hand-off with every analysed report
EntityMoon Consulting, LLC, Kalispell, Montana (its privacy policy)Aimosti Oy, Finland

What "conversion first" costs a genome

A whole-genome VCF carries a few million positions. Converting it to an array-style file keeps the few hundred thousand that a chip would have typed and discards the rest, including the rare variants that the clinical and carrier panels turn on. The result is a good chip file made from a genome, read well. It is not a genome read. Here, a 30x VCF is read as what it is, and the aligned reads add what no genotype list can carry: whether each gene was covered, and the true structure of CYP2D6. A variant-only file's silence is reported as silence; a gene the reads cannot cover is declined.

If you hold a chip file and custody is your first concern, Genetic Lifehacks is the honest recommendation, and our free in-browser file check shows what your particular export can and cannot support before you spend anything anywhere. If you hold a genome, conversion throws away the reason you sequenced.

Genetic Lifehacks is described from its own public pages as read on 3 September 2026. Prices are quoted as displayed that day, in the currency shown there, and features change. We do not speak for Genetic Lifehacks. If something here is out of date, tell us and we will correct it.

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.

See what your file supports, in your browser, before you decide.

Other comparisons: Promethease · SelfDecode · Gene2Rx · Sequencing.com · all five