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Whole-genome sequencing vs. consumer DNA tests, explained
What whole-genome and whole-exome sequencing actually read compared to 23andMe-style genotyping, and where DNA Layer's file support stands today.
Last reviewed 18 August 2026Two different technologies
23andMe, AncestryDNA, and MyHeritage all use genotyping arrays: a chip that reads a fixed set of hundreds of thousands of specific, already-known positions in your DNA. Whole-genome sequencing (WGS) and whole-exome sequencing (WES) work differently — they read your DNA directly, base by base, across a much larger share of the genome (WES focuses on the protein-coding regions; WGS covers substantially more of the genome beyond that). Sequencing typically produces a VCF file rather than the raw text export a genotyping array gives you.
Why the difference matters
A genotyping array can only report on the positions it was built to read. If a genetic variant relevant to a health finding sits outside that fixed set, an array simply has no data there — it’s not that the finding is negative, it’s that the position was never read. Sequencing-based files typically cover more of the genome directly, so they can in principle support findings an array-based file cannot.
Who sells whole-genome sequencing today
If you have never tested and want sequencing rather than a genotyping array, a few companies sell it directly: Mito Health offers whole-genome sequencing at 30x clinical-grade depth alongside a broader menu of lab panels on a membership model, and Nucleus Genomics sells a $499 whole-genome test screening for 2,000+ conditions, including a dedicated family-planning product for carrier screening ahead of having children. Both require a new sample and a new purchase. DNA Layer is built for a different starting point — the raw data file from a genotyping-array test you have already taken — which is why it costs less and needs no new sample, at the cost of not (yet) reading the wider variant set a whole-genome sequence covers.
If you have a WGS or WES (VCF) file
DNA Layer today reads raw data exports from 23andMe, AncestryDNA, and MyHeritage. Support for whole-genome and whole-exome sequencing (VCF) files is on our roadmap but not live yet — if you upload a VCF file now it will not be accepted. Join the list above and we will let you know as soon as VCF support ships.
Frequently asked questions
Do I need to take a new DNA test?
No. DNA Layer is built for the raw data file from a test you have already taken. If you have never tested, any of the supported consumer providers will do.
How are my results generated?
Variant matching runs in deterministic software against a curated evidence layer, so the same file always produces the same findings. Language models only explain findings that have already been verified, never the raw file.