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🧬 GWAS-MCP: Bioinformatics MCP Server

PyPI version License: MIT MCP

A powerful Model Context Protocol (MCP) server for GWAS and bioinformatics research. Seamlessly integrates with Claude Desktop and other MCP clients to provide AI-powered access to major biological databases.

30+ Tools 12+ Databases Python 3.10+


✨ Features

🔬 Protein & Gene Lookup

  • UniProt - Search proteins by name, gene, or ID
  • Ensembl - Gene information and variant details
  • NCBI Gene - Comprehensive gene database

🧪 Clinical & Variants

  • ClinVar - Clinical variant interpretations (pathogenic/benign)
  • GWAS Catalog - Genome-wide association studies
  • GTEx - Expression quantitative trait loci (eQTL)

🔗 Protein Interactions & Networks

  • STRING - Protein-protein interactions
  • InterPro - Protein domains and families

🏗️ Structures & Pathways

  • AlphaFold - AI-predicted protein structures
  • PDB - Experimental 3D structures
  • KEGG - Metabolic and signaling pathways

💊 Drug Discovery

  • Open Targets - Drug target validation & disease associations
  • PharmGKB - Pharmacogenomics & drug-gene interactions

🏥 Genetic Diseases

  • OMIM - Online Mendelian Inheritance in Man

🚀 Quick Start

Installation

pip install gwas-mcp

Claude Desktop Configuration

Add to your claude_desktop_config.json:

{
  "mcpServers": {
    "gwas-bioinformatics": {
      "command": "python",
      "args": ["-m", "gwas_mcp.server"]
    }
  }
}

Config file location:

  • Windows: %APPDATA%\Claude\claude_desktop_config.json
  • macOS: ~/Library/Application Support/Claude/claude_desktop_config.json
  • Linux: ~/.config/Claude/claude_desktop_config.json

Restart Claude Desktop

After adding the configuration, restart Claude Desktop to load the MCP server.


🛠️ Available Tools

Protein & Gene Tools

Tool Description
search_uniprot Search UniProt by protein name, gene, or ID
get_protein_details Get detailed protein info (function, domains, GO terms)
search_ncbi_gene Search NCBI Gene database
search_ensembl_gene Get gene location and details from Ensembl
get_variant_info Get SNP/variant info by rsID
get_interpro_domains Get protein domain information

Clinical & Variant Tools

Tool Description
search_clinvar Search ClinVar for clinical variants
get_clinvar_variant Get clinical interpretation for a variant
annotate_snps Annotate SNPs with functional consequences
query_gwas_catalog Query GWAS Catalog for associations
get_eqtl_data Get eQTL data from GTEx

Protein Interaction Tools

Tool Description
get_protein_interactions Find interacting proteins (STRING)
get_interaction_network Get network between multiple proteins
get_functional_enrichment Pathway/GO enrichment analysis

Structure & Pathway Tools

Tool Description
get_alphafold_structure Get AI-predicted structure
search_alphafold Search AlphaFold database
search_pdb_structures Search PDB for 3D structures
get_pdb_structure Get PDB structure details
search_kegg_pathway Search KEGG pathways
get_kegg_pathway Get pathway genes and details
get_gene_pathways Find pathways for a gene

Drug Discovery Tools

Tool Description
get_drug_targets Find drugs targeting a gene (Open Targets)
get_disease_associations Get disease associations with scores
search_open_targets Search genes, diseases, or drugs
search_pharmgkb Search PharmGKB database
get_drug_gene_interactions Get drug-gene interactions

Genetic Disease Tools

Tool Description
search_omim Search OMIM for genetic diseases
get_gene_diseases Get all diseases for a gene

💬 Example Prompts

Once configured, ask Claude naturally:

Protein & Gene Queries

"Get information about the BRCA1 gene"

"Search UniProt for hemoglobin"

"What protein has UniProt ID P53_HUMAN?"

Clinical Variants

"Is the BRCA1 variant rs80357906 pathogenic?"

"Search ClinVar for TP53 variants"

Protein Interactions

"What proteins interact with TP53?"

"Find functional enrichment for BRCA1, ATM, and CHEK2"

Structures & Pathways

"Get the AlphaFold structure for TP53"

"What pathways is BRCA1 involved in?"

"Search PDB for insulin structures"

Drug Discovery

"What drugs target EGFR?"

"What diseases is BRAF associated with?"

Genetic Diseases

"Search OMIM for cystic fibrosis"

"What diseases are linked to the CFTR gene?"


⚡ Performance Features

  • Smart Caching - API responses cached for 1 hour to improve speed
  • Async Operations - All API calls are non-blocking
  • Error Handling - Graceful handling of API failures

🔧 Development

From Source

# Clone the repository
git clone https://github.com/zaeyasa/gwas-mcp.git
cd gwas-mcp

# Install dependencies
pip install -e .

# Run the server
python -m gwas_mcp.server

Project Structure

gwas-mcp/
├── src/
│   └── gwas_mcp/
│       ├── server.py           # Main MCP server
│       ├── tools/
│       │   ├── protein_tools.py     # UniProt, NCBI, Ensembl
│       │   ├── clinical_tools.py    # ClinVar, STRING
│       │   ├── structure_tools.py   # PDB, KEGG, PharmGKB
│       │   └── advanced_tools.py    # AlphaFold, Open Targets, OMIM
│       └── resources/
│           └── db_resources.py      # Database resources
├── pyproject.toml
├── README.md
└── LICENSE

📊 Supported Databases

Database Type Description
UniProt Protein Protein sequences and annotations
Ensembl Gene/Variant Genome browser and variant data
NCBI Gene Gene Gene information database
ClinVar Clinical Clinical variant interpretations
GWAS Catalog GWAS Genome-wide association studies
GTEx Expression Expression QTL data
STRING Interactions Protein-protein interactions
InterPro Domains Protein families and domains
AlphaFold Structure AI-predicted structures
PDB Structure Experimental 3D structures
KEGG Pathways Metabolic and signaling pathways
Open Targets Drug Discovery Drug targets and disease associations
PharmGKB Pharmacogenomics Drug-gene interactions
OMIM Diseases Genetic disease database

🤝 Contributing

Contributions are welcome! Please feel free to submit a Pull Request.

  1. Fork the repository
  2. Create your feature branch (git checkout -b feature/amazing-feature)
  3. Commit your changes (git commit -m 'Add amazing feature')
  4. Push to the branch (git push origin feature/amazing-feature)
  5. Open a Pull Request

📄 License

This project is licensed under the MIT License - see the LICENSE file for details.


🙏 Acknowledgments

  • Model Context Protocol - The MCP specification
  • Anthropic - Claude AI and MCP development
  • All the amazing bioinformatics databases that make this possible

📬 Contact


Made with ❤️ for the bioinformatics community

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