Use when working with PharmVar (Pharmacogene Variation Consortium) to access curated pharmacogenomics variant data for CYP2D6, CYP2C19, CYP2C9, CYP3A5, DPYD, SLCO1B1, and other clinically actionable p
Use with AI
Install the MCP server or CLI to instantly fetch PharmVar Tools documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/pharmvar-tools
DPYD tools for pharmacogenomics analysis of dihydropyrimidine dehydrogenase variants. Supports star allele calling, diplotype-to-phenotype translation, and fluoropyrimidine (5-FU, capecitabine, tegafu
3 shared topics • 1 shared operation
Tools and workflows for accessing, querying, and analyzing data from the 1000 Genomes Project (1KGP) — the largest public catalog of human genetic variation with whole-genome sequences from 3,202 indi
2 shared topics • 1 shared operation
cyvcf2 — fast Cython-wrapped htslib library for reading, writing, and querying VCF/BCF variant files in Python. Provides numpy-backed genotype arrays (gt_types, gt_ref_depths, gt_alt_depths, gt_quals,
2 shared topics • 1 shared operation
Poetry is the Python dependency management and packaging tool for creating reproducible projects with pyproject.toml and poetry.lock. Use this skill for dependency resolution, virtual environment isol
2 shared topics • 1 shared operation
PubMed Database — NCBI's comprehensive biomedical literature database providing free access to over 37 million citations from MEDLINE, life science journals, and online books. Query via E-utilities RE
2 shared topics • 1 shared operation