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.
Simple genetic data analysis for GEDKeeper
A fun oracle for Eurogenes K13.
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.
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
Your DNA, decoded on your device — turn your 23andMe/AncestryDNA raw data into a beautiful traits report, 100% in your browser. Nothing uploaded.
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.
Open-source, privacy-first DNA analyzer — upload your raw DNA data (23andMe, AncestryDNA, MyHeritage) and get AI-powered health & trait insights. All processing runs in your browser.
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.
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.
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