gnomancerSynthetic data · no real person

Your raw DNA file → a readable report.

A real run on an entirely synthetic sample. No upload or sign-in.

Try gnomancer
Your computer does the analysis

One command.
One local report.

Read an export from AncestryDNA, 23andMe, MyHeritage, FTDNA, LivingDNA, or a VCF.

This demo uses 20,342 synthetic sites generated with the repository’s example script. No personal DNA file was used.

Actual synthetic-sample run · shortened paths
$ gnomancer demo_AncestryDNA.txt \
    --out demo_report --no-y --no-mt \
    --no-clinvar --no-pharmcat

✓ AncestryDNA · build 37 · 20,342 SNPs
✓ Quality metrics
✓ Runs of homozygosity
✓ Marker panel

Report: demo_report/REPORT.html

This is illustrative synthetic data, not medical advice. Haplogroup callers, ClinVar, and PharmCAT were skipped in this lightweight run. The sample uses artificial genomic positions and is unsuitable for validating those analyses.

Watch the 28-second walkthrough

A captioned walkthrough of the four scenes above. All genotypes are synthetic. Download MP4 · Sample provenance