Helps you browse through and interpret your genotype data
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Updated
Jan 29, 2023 - JavaScript
Helps you browse through and interpret your genotype data
🧬 Open-source genotype analysis toolkit
An Open Source Web Application for Genetic Data (SNPs) Data Crawling
🌳 Scalable ancestry from genomic data
Tools to work with 23andMe and AncestryDNA raw files
🧬 Open-source genotype analysis toolkit. The open-source Promethease replacement.
Privacy-first genetic exploration dashboard. Analyze raw DNA from 23andMe, AncestryDNA, MyHeritage, and Genera against ClinVar + PharmGKB — entirely on your machine. Optional local AI interpretation via Ollama and PT-BR neural translation via Argos.
Simple genetic data analysis for GEDKeeper
A fun oracle for Eurogenes K13.
Collection of scripts and Jupyter Notebooks created for working with DNA matches
Convert 23andMe DNA raw data to AncestryDNA, MyHeritage, FamilyTreeDNA formats
convert genotype array output into annotated IBD segments
Local-first desktop DNA explorer for AncestryDNA and 23andMe. Trait reports, pharmacogenomics, optional Ollama chat, and an MCP server — DNA stays on your machine.
Which SNPs are actually present in consumer DNA raw data: rsID coverage across 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA and LivingDNA chips, built from public chip manifests. Includes notable gaps where a reported result is structurally impossible.
Read raw DNA exports from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA and LivingDNA: detect service and chip, count markers, check rsID coverage. Go library and CLI, fully local — your genome file never leaves your machine.
Your DNA, decoded on your device — turn your 23andMe/AncestryDNA raw data into a beautiful traits report, 100% in your browser. Nothing uploaded.
Turn raw 23andMe/AncestryDNA data into a private, local HTML health report — clinical variants (ClinVar, AlphaMissense), pharmacogenomics (PharmGKB), and polygenic risk scores (PGS Catalog), plus an optional AI summary. Runs 100% locally; your genome is never uploaded.
Personal genomics analysis toolkit: ingest consumer DNA raw data, impute against 1000 Genomes, and produce an evidence-graded ledger of pharmacogenomic, carrier-screening, trait, polygenic-score, and haplogroup findings — all locally.
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