Text mining for pharmacogenomic associations for PharmGKB

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.

A comprehensive genetic health analysis pipeline that processes 23andMe raw data to generate detailed health reports using Claude Code or other AI Agents.

MCP server for pharmacogenomics — ClinVar, PharmGKB, gnomAD, OpenTargets, and clinical trials from Claude

ClinVar-first VCF triage and reporting tool with optional PharmGKB enrichment.

Cross-referencing FDA FAERS drug safety signals with PharmGKB pharmacogenomic annotations to identify genotype-dependent adverse events with evidence-graded convergence scoring

Python toolkit for retrieving and integrating pharmacogenomic data from ClinVar, PharmGKB, and DGIdb.

Map disease, drug & gene interactions.

India-first, privacy-first genomics toolkit for local DNA analysis and personalized health insights — open-source Community Edition