Chromosome visualization for the web
Easy genetic ancestry predictions in Python
A tool to create genomic reports based on 23andMe data.
Telomere-2-Telomere Genome from Saudi Arabia
Tool and library with ui to compute polygenic risk scores
Whole genome sequencing analysis pipeline for consumer hardware. 100% local, Docker-powered, free and open source.
Privacy-first polygenic risk score analysis. Upload your DNA, get trait scores — all processing happens on your device. Built on DuckDB WASM, Web Components, and the PGS Catalog. No accounts, no servers, no data leaves your browser.
Self-hosted genetics processing platform: VCF generation, imputation merging, PGS calculation. 60× faster than R, LUKS encrypted, air-gapped worker. Rust + PostgreSQL.
🧬 Open-source genetic analysis toolkit. Analyze your WGS/VCF data locally and privately. 500+ variants across fitness, health, traits & more. For education & fun only - not for clinical use.
Local-first 23andMe and DTC DNA raw data to VCF 4.2 converter with PySide6 GUI, GRCh37/GRCh38 detection, and dbSNP/FASTA REF lookup
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.
Yale Gradute School module CBB752 final group project by Jiaqi Li, Keyi Li, and Anna Su.
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.
Analyze whole genome sequencing data on consumer hardware with no cloud accounts, subscriptions, or bioinformatics degree needed
Local-first pipeline for annotating consumer DNA raw data against ClinVar, GWAS Catalog, and SNPedia/Promethease. Reconciles multiple arrays, enriches variants, assigns haplogroups — and runs entirely on your machine, so raw genomes never leave it.
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