About Nexonco Mcp
Nexonco is an MCP server that provides access to clinical evidence from the CIViC database. It is aimed at precision oncology and research use, with flexible search across variants, diseases, drugs and phenotypes.
Key features
- 01Search evidence by variant, disease, drug or phenotype
- 02Filter by evidence type, direction and rating
- 03Summary statistics and top ten evidence entries
- 04Source citations and research-only disclaimer
Use cases
- 01Find predictive evidence for colorectal cancer therapies with KRAS mutations
- 02Review studies on a specific drug in leukemia
- 03Survey therapies linked to pancreatic cancer evidence
MCP support
Nexonco exposes a search_clinical_evidence tool over MCP, which MCP clients can call to receive a formatted evidence report.
Configuration
Local server config is the same for every client. Copy it into your client’s MCP config file.
We haven’t collected a package or remote endpoint for this server. Follow the instructions in the project README.
Tools
Local servers expose tools only once running on your machine, and the maintainer has not provided a tool list.
Details
From the project READMEDemo
https://github.com/user-attachments/assets/02129685-5ba5-4b90-89e7-9d4a39986210
Setup
Prerequisites
- uv or Docker
- Claude Desktop (for MCP integration)
Setup Guides
For detailed setup instructions, refer to the following documentation:
-
NANDA Host Setup
Seedocs/nanda-server-setup.mdfor backend configuration and local registration of the NANDA Server. -
Claude Desktop Setup
Seedocs/claude-desktop-setup.mdfor 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): IfTrue, only includes evidence with a rating > 3 (max 5).
Output
The tool returns a formatted string with four sections:
- Summary Statistics:
- Total evidence items
- Average evidence rating
- Top 3 diseases, genes, variants, therapies, and phenotypes (with counts)
- Top 10 Evidence Entries:
- Lists the highest-rated evidence items with details like disease, phenotype, gene/variant, therapy, description, type, direction, and rating.
- Sources & Citations:
- Citations and URLs for the sources of the top 10 evidence entries.
- 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
- Model Context Protocol
- NANDA: The Internet of AI Agents
- CIViC - Clinical Interpretation of Variants in Cancer
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
- Obada Qasem (@obadaqasem), Nexgene AI
- Kutsal Ozkurt (@Goodsea), Nexgene AI
Comments
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