COSMIC (Catalogue Of Somatic Mutations In Cancer) is the authoritative curated database of somatic mutations driving human cancer, maintained by the Wellcome Sanger Institute. Use this skill for query
Use with AI
Install the MCP server or CLI to instantly fetch COSMIC documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/cosmic
LipidFinder routing skill for lipidomics LC-MS feature filtering and lipid annotation. Use this skill when users mention LipidFinder, LipidSearch, LIPID MAPS, LMSD, lipidomics feature annotation, lipi
1 shared topic • 3 shared operations
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
1 shared topic • 2 shared operations
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 • 2 shared operations
Tools for manipulating next-generation sequencing data stored in SAM/BAM/CRAM format, including sorting, indexing, and format conversion.
1 shared topic • 2 shared operations
Sarek — nf-core Nextflow pipeline for germline and somatic variant calling from whole-genome sequencing (WGS), whole-exome sequencing (WES), and targeted sequencing data. Supports multiple variant cal
1 shared topic • 2 shared operations