genomics-mcp
OfficialRelated Servers
Alternatives to genomics-mcp
No user-submitted related servers found.
Related Servers
- AlicenseNot gradedqualityBmaintenanceEnables researchers to query DigitalBrain data catalogs, brain region profiles, gene expression summaries, and paper evidence, and download approved results through MCP-compatible clients.MIT

mentu-navigator-mcpofficial
AlicenseNot gradedqualityCmaintenanceProvides read-only, provenance-first repository navigation for agents and humans, with ranked lexical retrieval, exact query, document handles, symbol context, and change impact analysis.63 npmApache 2.0- AlicenseNot gradedqualityCmaintenanceEnables querying the gnomAD genome aggregation database for variant, gene, and region information.2 npmMIT
- AlicenseNot gradedqualityCmaintenanceEnables querying GTEx gene expression, eQTL, and tissue data through an MCP gateway.2 npmMIT
- AlicenseNot gradedqualityCmaintenanceEnables local read-only search and retrieval of approved, current evidence via hybrid lexical and dense methods, with tools to get exact source spans, answer from cited passages, and create and verify recheckable evidence packets.MIT
- FlicenseAqualityDmaintenanceEnables interaction with synthetic NIH-style clinical research data through tools for searching publications, querying patient metadata, analyzing AAA measurements, and retrieving protocol guidance.5-
TDQS
Scored across 23 tools
Each tool describes a specific resource and action, so most are easy to distinguish. The only potential confusions are resolve_identifier versus lookup_variant/lookup_gene/lookup_protein and compare_samples overlapping with get_coverage/get_variants, but the descriptions resolve most ambiguity.
All 23 tools follow a consistent snake_case verb_noun pattern: list_sources, get_reads, fetch_file, lookup_variant, etc. Verbs vary by operation, but the naming convention is uniform and predictable.
23 tools is in the heavy 16-25 range and feels a bit large, though genomics data access is a broad domain that can justify many operations. Several read/query tools could be consolidated, but the count is not wildly excessive.
Although the planned set covers a wide range of genomics operations, 22 of 23 tools are explicitly not implemented in this build and return 'unsupported' errors. Agents can list sources but cannot actually search, fetch, query, or annotate anything, making the working surface severely incomplete.