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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-$p$ < 0.05) for LLM tools to interpret.

Smithery

Installation

Claude Desktop

Download the latest MCPB bundle (.mcpb file) and install it via ☰ (top left) -> File -> Settings, then drag and drop the file into the Settings window.

Cursor / VS Code

Use the buttons below to install with default settings:

Install MCP Server Add to VS Code Add to VS Code Insiders

Claude Code

claude mcp add enrichr-mcp-server -- npx -y enrichr-mcp-server

Or install as a Claude Code plugin:

/plugin install enrichr-mcp-server

Smithery

npx -y @smithery/cli install enrichr-mcp-server --client claude

Manual 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

  • Library Catalog: Browse 200+ libraries by category via MCP resources

  • 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. No network call needed — searches locally across all library names and descriptions.

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)

  • 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

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 <libs>

-l

Comma-separated list of Enrichr libraries to query

pop

--max-terms <num>

-m

Maximum terms to show per library

50

--format <format>

-f

Output format: detailed, compact, minimal

detailed

--output <file>

-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"]
    }
  }
}

When using the default -l pop configuration:

Library

Description

GO_Biological_Process_2025

Gene Ontology terms describing biological objectives accomplished by gene products.

KEGG_2021_Human

Metabolic and signaling pathways from KEGG for human.

Reactome_2022

Curated and peer-reviewed pathways covering signaling, metabolism, and disease.

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_2023

Genome-wide association study results linking genes to traits.

Human_Phenotype_Ontology

Standardized vocabulary of phenotypic abnormalities associated with human diseases.

STRING_Interactions_2023

Protein interactions from STRING including experimental and predicted.

DrugBank_2022

Drug targets from DrugBank including approved and experimental compounds.

CellMarker_2024

Manually curated cell type markers for human and mouse.

API Details

This server uses the Enrichr API:

  • Add List Endpoint: https://maayanlab.cloud/Enrichr/addList

  • Enrichment Endpoint: https://maayanlab.cloud/Enrichr/enrich

  • Supported Libraries: All libraries available through the Enrichr web interface

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 inspector

Requirements

  • 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

  • Enrichr

  • Model Context Protocol

  • MCP TypeScript SDK

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security – no known vulnerabilities
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license - not found
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quality - not tested

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