M-CAP (Mendelian Clinically Applicable Pathogenicity) is a clinical-grade pathogenicity classifier for rare human missense variants. Developed at the Bejerano Lab (Stanford), it applies a gradient-boo
Use with AI
Install the MCP server or CLI to instantly fetch M Cap documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/m-cap
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2 shared topics • 1 shared operation
VEP (Ensembl Variant Effect Predictor) — gold-standard tool for annotating and predicting the functional effects of genomic variants on genes, transcripts, and protein sequences. Provides consequence
1 shared topic • 1 shared operation
Ensembl Database — EMBL-EBI's comprehensive genome annotation database covering 300+ species with gene models, variants, regulatory features, and comparative genomics. Query via REST API at rest.ensem
1 shared topic
TCGAbiolinks for searching, downloading, and analyzing cancer genomics data from the NCI Genomic Data Commons (GDC). Routes tasks for GDCquery/GDCdownload, data preparation with GDCprepare, differenti
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Zarr — chunked, compressed N-dimensional arrays for Python with cloud-native storage. Provides hierarchical groups, pluggable compression codecs (Blosc, Zstd, Gzip), sharding for large-scale datasets,
1 shared topic