BioMCP (Typescript)
Agent-first rewrite of genomeoncology's BioMCP in TypeScript to provide next-gen biomedical data access for agents.
BioMCP
A high-performance MCP server that gives LLMs access to 24 biomedical tools federated across 50+ upstream APIs — genes, variants, drugs, diseases, literature, and clinical trials in a single integration.
Adapted from the BioMCP Rust with agent-first development approach and enhancements. Kudos to the original authors.
Highlights
- 24 tools across 7 domains — search, retrieve, and cross-reference biomedical entities
- 50+ upstream sources — MyGene, MyVariant, MyChem, MyDisease, ClinVar, gnomAD, UniProt, Reactome, OpenTargets, CIViC, OncoKB, DisGeNET, GTEx, STRING, DGIdb, ClinicalTrials.gov, PubMed, EuropePMC, Semantic Scholar, PubTator, LitSense, Monarch Initiative, OpenFDA, NIH Reporter, AlphaGenome, and more
- Section-based fetching —
entityGet(id, sections)fans out to multiple sources with per-section timeouts and graceful degradation (failed sections return{ _error }instead of crashing) - Federated article search — queries 5 literature backends simultaneously with PMID/PMCID/DOI deduplication
- Zero-config startup — works out of the box; optional API keys unlock higher rate limits and premium data
- 195 tests — 131 unit tests (mocked) + 64 integration tests (live APIs via in-process MCP client)
Quick Start
Install and build
git clone <repo-url> && cd biomcp-ts
make install build-bundle
Configure with Claude Desktop
Add to your Claude Desktop claude_desktop_config.json:
{
"mcpServers": {
"biomcp": {
"command": "npx",
"args": ["biomcp"]
}
}
}
Or from a local checkout:
{
"mcpServers": {
"biomcp": {
"command": "node",
"args": ["/path/to/biomcp-ts/dist/bundle.js"]
}
}
}
Direct stdio
npm start
Any MCP-compatible client
BioMCP speaks standard MCP over stdio. Point any MCP client at the biomcp binary or node dist/bundle.js.
Available Tools
Gene (7)
| Tool | Description |
|---|---|
gene_search | Search genes by symbol, name, or keyword with type/chromosome filters |
gene_get | Get detailed gene info by HGNC symbol with optional sections (pathways, protein, GO, interactions, expression, constraint, druggability, clinical evidence, disease associations, funding) |
gene_diseases | Get diseases associated with a gene (DisGeNET / OpenTargets) |
gene_drugs | Find drugs targeting a gene (OpenTargets) |
gene_trials | Find clinical trials for a gene |
gene_articles | Find articles about a gene |
gene_enrich | Pathway enrichment analysis for a gene list (Reactome) |
Variant (4)
| Tool | Description |
|---|---|
variant_search | Search variants by rsid, HGVS, gene, ClinVar significance, frequency, CADD |
variant_get | Get detailed variant info with optional sections (frequency, predictions, clinical, alphagenome_scores) |
variant_oncokb | Get OncoKB cancer variant annotations (requires ONCOKB_TOKEN) |
variant_trials | Find clinical trials for a variant |
Drug (3)
| Tool | Description |
|---|---|
drug_search | Search drugs by name, mechanism, or keyword |
drug_get | Get detailed drug info with optional sections (us_regulatory, eu_regulatory, who_regulatory, safety, targets, indications) |
drug_trials | Find clinical trials for a drug |
Disease (4)
| Tool | Description |
|---|---|
disease_search | Search diseases by name, phenotype, or keyword |
disease_get | Get detailed disease info by ID (DOID, MONDO, OMIM, etc.) with optional sections (gene_associations, phenotypes, pathways, survival) |
disease_drugs | Get drugs for a disease (OpenTargets) |
disease_trials | Get clinical trials for a disease (ClinicalTrials.gov) |
Article (2)
| Tool | Description |
|---|---|
article_search | Federated literature search across PubMed, EuropePMC, Semantic Scholar, PubTator, and LitSense |
article_get | Get detailed article info by PMID with optional sections (open_access, annotations, citation_graph) |
Trial (2)
| Tool | Description |
|---|---|
trial_search | Search clinical trials by condition, intervention, status, or phase |
trial_get | Get detailed trial info by NCT ID with optional sections (eligibility, locations, outcomes) |
Utility (2)
| Tool | Description |
|---|---|
discover | Free-text concept resolution across all entity types |
batch_get | Retrieve multiple entities in parallel |
Development
make # Show available targets
make install # Install dependencies
make build-bundle # Compile and bundle into dist/bundle.js
make typecheck # Type-check without emitting
make test # Run unit tests (fast, mocked)
make test-integration # Run integration tests (live APIs, ~60s)
make test-all # Run all tests
make clean # Remove build artifacts
Environment Variables
All keys are optional. BioMCP works without any keys — they unlock higher rate limits and additional data sources.
| Variable | Source | Benefit |
|---|---|---|
NCBI_API_KEY | NCBI | Higher PubMed / NCBI rate limits |
S2_API_KEY | Semantic Scholar | Semantic Scholar API access |
OPENFDA_API_KEY | OpenFDA | OpenFDA API access |
NCI_API_KEY | NCI CTS | NCI Clinical Trials API |
ONCOKB_TOKEN | OncoKB | OncoKB cancer variant annotations |
DISGENET_API_KEY | DisGeNET | Disease-gene associations |
UMLS_API_KEY | UMLS | UMLS terminology services |
ALPHAGENOME_API_KEY | AlphaGenome | AlphaGenome variant scores |
License
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