nexonco-mcp

nexonco-mcp

48
research_and_datadatabases

Nexonco is an MCP server developed by Nexgene Research that enables advanced searches for clinical evidence from the CIViC database. It is designed to support precision oncology through flexible querying of medical domains. The project focuses on providing comprehensive reports for research purposes.

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Nexonco by Nexgene Research is an MCP server for accessing clinical evidence from the CIViC (Clinical Interpretation of Variants in Cancer) database. It enables fast, flexible search across variants, diseases, drugs, and phenotypes to support precision oncology.

PyPI NANDA License

Demo

https://github.com/user-attachments/assets/02129685-5ba5-4b90-89e7-9d4a39986210

Watch full video here: Youtube

Setup

Prerequisites

  • uv or Docker
  • Claude Desktop (for MCP integration)

Setup Guides

For detailed setup instructions, refer to the following documentation:

  • NANDA Host Setup
    See docs/nanda-server-setup.md for backend configuration and local registration of the NANDA Server.

  • Claude Desktop Setup
    See docs/claude-desktop-setup.md for guidance on configuring the local development environment and MCP integration.

These guides include all required steps, environment configurations, and usage notes to get up and running.

Tool List

search_clinical_evidence: A MCP tool for querying clinical evidence data that returns formatted reports.

Input Schema

The tool accepts the following optional parameters:

  • disease_name (str): Filter by disease (e.g., "Lung Non-small Cell Carcinoma").
  • therapy_name (str): Filter by therapy or drug (e.g., "Cetuximab").
  • molecular_profile_name (str): Filter by gene or variant (e.g., "EGFR L858R").
  • phenotype_name (str): Filter by phenotype (e.g., "Chest Pain").
  • evidence_type (str): Filter by evidence type (e.g., "PREDICTIVE", "DIAGNOSTIC").
  • evidence_direction (str): Filter by evidence direction (e.g., "SUPPORTS").
  • filter_strong_evidence (bool): If True, only includes evidence with a rating > 3 (max 5).

Output

The tool returns a formatted string with four sections:

  1. Summary Statistics:
    • Total evidence items
    • Average evidence rating
    • Top 3 diseases, genes, variants, therapies, and phenotypes (with counts)
  2. Top 10 Evidence Entries:
    • Lists the highest-rated evidence items with details like disease, phenotype, gene/variant, therapy, description, type, direction, and rating.
  3. Sources & Citations:
    • Citations and URLs for the sources of the top 10 evidence entries.
  4. Disclaimer:
    • A note stating the tool is for research purposes only, not medical advice.

Sample Usage

  • "Find predictive evidence for colorectal cancer therapies involving KRAS mutations."
  • "Are there studies on Imatinib for leukemia?"
  • "What therapies are linked to pancreatic cancer evidence?"

Acknowledgements

License

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

Disclaimer

⚠️ This tool is intended exclusively for research purposes. It is not a substitute for professional medical advice, diagnosis, or treatment.

Contributors