First public release. A genomic-report generator that turns raw consumer DNA data into a ~50-page research/educational PDF across 33 domains and 413 annotated SNPs.
Validated
End-to-end on real exports from FTDNA, AncestryDNA (V2.0), 23andMe (v5), and MyHeritage — all GRCh37 — plus the AncestryDNA + MyHeritage dual-dataset merge. .gz inputs are handled transparently.
Not yet supported / untested
VCF is not implemented; LivingDNA is experimental and untested; build-38 files and other platform vintages are unvalidated (see README → Supported Input Formats).
Highlights
- ROH corrected — terminal runs emitted, autosomes-only scan, and a 1 Mb max-gap split so centromere SNP-deserts no longer inflate F_ROH. (F_ROH values differ from earlier builds — re-baseline if you compare across reports.)
- Cross-platform robustness — AncestryDNA platform label fixed; §35 key-finding checks made allele-order-insensitive (AncestryDNA reports arbitrary allele order).
- Safety — a CYP2C9 no-call is no longer reported as a normal warfarin metaboliser.
- Honesty — report coverage labels disambiguated; supported-format claims corrected.
Not medical advice
Research and informational use only. Confirm any finding with an accredited clinical laboratory. See the disclaimer in README and the per-report disclaimer.