enrichr-mcp-server
Enrichr MCP Server
Documentation
Enrichr MCP Server
A Model Context Protocol (MCP) server that provides gene set enrichment analysis using the Enrichr API. This server supports all available gene set libraries from Enrichr and returns only statistically significant results (corrected-$p$ File -> Settings`, then drag and drop the file into the Settings window.
Cursor / VS Code
Use the buttons below to install with default settings:
Claude Code
claude mcp add enrichr-mcp-server -- npx -y enrichr-mcp-serverOr install as a Claude Code plugin:
/plugin install enrichr-mcp-serverSmithery
npx -y @smithery/cli install enrichr-mcp-server --client claudeManual Configuration
Add to your MCP client config (e.g., `.cursor/mcp.json`):
{
"mcpServers": {
"enrichr-server": {
"command": "npx",
"args": ["-y", "enrichr-mcp-server"]
}
}
}Features
- Two Tools: `enrichr_analysis` for running enrichment, `suggest_libraries` for discovering relevant libraries
- Custom Background Correction: Test against your own background gene set (e.g. only the genes expressed in your assay) instead of the whole genome
- Live Library Catalog: The library list is fetched from Enrichr at runtime, so new releases appear automatically and retired libraries are never suggested
- Guided Workflow: `enrichment_analysis` prompt for end-to-end analysis with interpretation
- 22 Library Categories: Programmatic category mapping for all libraries (pathways, cancer, kinases, etc.)
- Parallel Library Queries: All libraries queried in parallel for fast multi-database analysis
- Structured Output: Returns both human-readable text and structured JSON for programmatic use
- Configurable Output Formats: Detailed, compact, or minimal to manage token usage
- TSV Export: Save complete results to TSV files
Tools
`suggest_libraries`
Discover the most relevant Enrichr libraries for a research question. Use this before `enrichr_analysis` to pick the best libraries for your specific topic. Searches Enrichr's live library catalog, so it never recommends a library that Enrichr has retired. When two libraries are equally relevant, the newer vintage ranks first (`GO_Biological_Process_2026` over `..._2021`).
Parameters:
- `query` (required): Research context (e.g., "DNA repair", "breast cancer drug resistance")
- `category` (optional): Filter by category (e.g., `cancer`, `pathways`, `kinases`)
- `maxResults` (optional): Max results to return (default: 10, max: 50)
Returns:
- Ranked list of libraries with relevance scores, categories, and descriptions
- Structured JSON with suggestions array
`enrichr_analysis`
Perform enrichment analysis across multiple Enrichr libraries in parallel.
Parameters:
- `genes` (required): Array of gene symbols (e.g., `["TP53", "BRCA1", "EGFR"]`) — minimum 2
- `libraries` (optional): Array of Enrichr library names to query (defaults to configured libraries)
- `background` (optional): Custom background gene set — minimum 20 genes. See below.
- `description` (optional): Description for the gene list
- `maxTerms` (optional): Maximum terms per library (default: 50)
- `format` (optional): Output format: `detailed`, `compact`, `minimal`
- `outputFile` (optional): Path to save complete results as TSV file
Returns:
- Text content with formatted significant terms (name, p-values, odds ratio, combined score, overlapping genes)
- Structured JSON output with full result data, including `backgroundCorrected` per library
Background correction
By default Enrichr tests your gene list against the whole genome. If your genes
were drawn from a restricted universe — only the genes expressed in your tissue, or
a targeted panel — the whole-genome default overstates significance, often by many
orders of magnitude. Pass `background` with the universe the list was drawn from:
{
"genes": ["TP53", "BRCA1", "ATM", "CHEK2"],
"background": ["TP53", "BRCA1", "ATM", "CHEK2", "ACTB", "GAPDH", "..."],
"libraries": ["GO_Biological_Process_2026"]
}The difference is not cosmetic. For a 16-gene DNA-damage list, the top GO term moves
from an adjusted p of 1.2e-16 (whole genome) to 1.8e-5 (48-gene background), and the
number of "significant" terms drops from 359 to 10.
Background correction runs against Enrichr's separate `speedrichr` service, which is
intermittently unavailable. Failures are retried; if they persist, the library falls
back to uncorrected whole-genome p-values, and the result is flagged
`backgroundCorrected: false` with a loud `WARNING` in the text output. **A fallback
result is never presented as if it were background-corrected.**
Resources
| URI | Description |
|---|---|
| `enrichr://libraries` | Full library catalog organized by category |
| `enrichr://libraries/{category}` | Libraries for a specific category (e.g., `enrichr://libraries/cancer`) |
Prompts
`enrichment_analysis`
Guided workflow for gene set enrichment analysis. Accepts a gene list and optional research context, then walks through library selection, analysis, and interpretation.
Arguments:
- `genes` (required): Gene symbols, comma or newline separated
- `context` (optional): Research context for library selection (triggers `suggest_libraries` step)
Library Categories
All 200+ libraries are organized into 22 categories:
| Category | Examples |
|---|---|
| `transcription` | ChEA_2022, ENCODE_TF_ChIP-seq_2015, TRANSFAC_and_JASPAR_PWMs |
| `pathways` | KEGG_2021_Human, Reactome_2022, WikiPathways_2023_Human, MSigDB_Hallmark_2020 |
| `ontologies` | GO_Biological_Process_2025, GO_Molecular_Function_2025, Human_Phenotype_Ontology |
| `diseases_drugs` | GWAS_Catalog_2023, DrugBank_2022, OMIM_Disease, DisGeNET |
| `cell_types` | GTEx_Tissue_Expression_Up, CellMarker_2024, Tabula_Sapiens |
| `microRNAs` | TargetScan_microRNA_2017, miRTarBase_2022, MiRDB_2019 |
| `epigenetics` | Epigenomics_Roadmap_HM_ChIP-seq, JASPAR_2022, Cistrome_2023 |
| `kinases` | KEA_2015, PhosphoSitePlus_2023, PTMsigDB_2023 |
| `gene_perturbations` | LINCS_L1000_CRISPR_KO_Consensus_Sigs, CRISPR_GenomeWide_2023 |
| `metabolomics` | HMDB_Metabolites, Metabolomics_Workbench_2023, SMPDB_2023 |
| `aging` | Aging_Perturbations_from_GEO_down, GenAge_2023, Longevity_Map_2023 |
| `protein_families` | InterPro_Domains_2019, Pfam_Domains_2019, UniProt_Keywords_2023 |
| `computational` | Enrichr_Submissions_TF-Gene_Coocurrence, ARCHS4_TF_Coexp |
| `literature` | Rummagene_signatures, AutoRIF, GeneRIF |
| `cancer` | COSMIC_Cancer_Gene_Census, TCGA_Mutations_2023, OncoKB_2023, GDSC_2023 |
| `single_cell` | Human_Cell_Landscape, scRNAseq_Datasets_2023, SingleCellSignatures_2023 |
| `chromosome` | Chromosome_Location, Chromosome_Location_hg19 |
| `protein_interactions` | STRING_Interactions_2023, BioGRID_2023, IntAct_2023, MINT_2023 |
| `structural` | PDB_Structural_Annotations, AlphaFold_2023 |
| `immunology` | ImmuneSigDB, ImmPort_2023, Immunological_Signatures_MSigDB |
| `development` | ESCAPE, Developmental_Signatures_2023 |
| `other` | MSigDB_Computational, HGNC_Gene_Families, Open_Targets_2023 |
Use `suggest_libraries` to search across all categories, or read `enrichr://libraries/{category}` for the full list in any category.
Configuration
Command Line Options
| Option | Short | Description | Default |
|---|---|---|---|
| `--libraries ` | `-l` | Comma-separated list of Enrichr libraries to query | `pop` |
| `--max-terms ` | `-m` | Maximum terms to show per library | `50` |
| `--format ` | `-f` | Output format: `detailed`, `compact`, `minimal` | `detailed` |
| `--output ` | `-o` | Save complete results to TSV file | _(none)_ |
| `--compact` | `-c` | Use compact format (same as `--format compact`) | _(flag)_ |
| `--minimal` | Use minimal format (same as `--format minimal`) | _(flag)_ | |
| `--help` | `-h` | Show help message | _(flag)_ |
Format Options
- `detailed`: Full details including p-values, odds ratios, and gene lists (default)
- `compact`: Term name + p-value + gene count (saves ~50% tokens)
- `minimal`: Just term name + p-value (saves ~80% tokens)
Environment Variables
| Variable | Description | Example |
|---|---|---|
| `ENRICHR_LIBRARIES` | Comma-separated list of libraries | `GO_Biological_Process_2025,KEGG_2021_Human` |
| `ENRICHR_MAX_TERMS` | Maximum terms per library | `20` |
| `ENRICHR_FORMAT` | Output format | `compact` |
| `ENRICHR_OUTPUT_FILE` | TSV output file path | `/tmp/enrichr_results.tsv` |
Note: CLI arguments take precedence over environment variables.
Multiple Server Instances
Set up different instances for different research contexts:
{
"mcpServers": {
"enrichr-pathways": {
"command": "npx",
"args": ["-y", "enrichr-mcp-server", "-l", "GO_Biological_Process_2025,KEGG_2021_Human,Reactome_2022"]
},
"enrichr-disease": {
"command": "npx",
"args": ["-y", "enrichr-mcp-server", "-l", "Human_Phenotype_Ontology,OMIM_Disease,ClinVar_2019"]
}
}
}Popular Libraries (Default)
When using the default `-l pop` configuration:
| Library | Description |
|---|---|
| `GO_Biological_Process_2026` | Current Gene Ontology biological process terms. |
| `KEGG_2026` | Current KEGG metabolic and signaling pathways. |
| `Reactome_Pathways_2024` | Current Reactome release — curated, peer-reviewed pathways. |
| `MSigDB_Hallmark_2020` | Hallmark gene sets representing well-defined biological states and processes. |
| `ChEA_2022` | ChIP-seq experiments identifying transcription factor-gene interactions. |
| `GWAS_Catalog_2025` | Genome-wide association study results linking genes to traits. |
| `Human_Phenotype_Ontology` | Standardized vocabulary of phenotypic abnormalities associated with human diseases. |
| `PPI_Hub_Proteins` | Highly connected hub proteins from protein-protein interaction networks. |
| `DGIdb_Drug_Targets_2024` | Drug-gene interactions from the Drug Gene Interaction Database. |
| `CellMarker_2024` | Manually curated cell type markers for human and mouse. |
API Details
This server uses the Enrichr API:
- Add List: `https://maayanlab.cloud/Enrichr/addList`
- Enrichment: `https://maayanlab.cloud/Enrichr/enrich`
- Library Catalog: `https://maayanlab.cloud/Enrichr/datasetStatistics` — fetched at runtime and cached for 24h, so the library list is never stale
- Background-corrected enrichment: `https://maayanlab.cloud/speedrichr/api/{addList,addbackground,backgroundenrich}`
- Supported Libraries: Every library Enrichr currently serves (228 at time of writing)
Note: Enrichr emits bare `Infinity` literals for the odds ratio when a term's overlap
with the background is complete — which is not valid JSON. This server parses those
responses correctly; a naive `JSON.parse` on the raw response will throw.
Development
npm run build # Build TypeScript
npm test # Run tests (unit + integration + MCP protocol)
npm run test:watch # Run tests in watch mode
npm run watch # Auto-rebuild on file changes
npm run inspector # Debug with MCP inspectorRequirements
- Node.js 18+
- Internet connection for Enrichr API access
License
MIT
References
- Chen EY, Tan CM, Kou Y, Duan Q, Wang Z, Meirelles GV, Clark NR, Ma'ayan A. Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool. BMC Bioinformatics. 2013; 128(14).
- Kuleshov MV, Jones MR, Rouillard AD, Fernandez NF, Duan Q, Wang Z, Koplev S, Jenkins SL, Jagodnik KM, Lachmann A, McDermott MG, Monteiro CD, Gundersen GW, Ma'ayan A. Enrichr: a comprehensive gene set enrichment analysis web server 2016 update. Nucleic Acids Research. 2016; gkw377.
- Xie Z, Bailey A, Kuleshov MV, Clarke DJB., Evangelista JE, Jenkins SL, Lachmann A, Wojciechowicz ML, Kropiwnicki E, Jagodnik KM, Jeon M, & Ma'ayan A. Gene set knowledge discovery with Enrichr. Current Protocols, 1, e90. 2021. doi: 10.1002/cpz1.90
Frequently asked questions
What is enrichr-mcp-server?
enrichr-mcp-server is Enrichr MCP Server
How do I install enrichr-mcp-server?
Open the GitHub repository and follow its README. Most MCP servers are added to your client's MCP config, then called by your agent.
Is enrichr-mcp-server open source?
Yes — it is hosted on GitHub at https://github.com/tianqitang1/enrichr-mcp-server and has 15 stars.
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