BioMCP is a server implementation that provides structured access to key biomedical databases through a unified interface. Developed by GenomOncology, it connects to ClinicalTrials.gov, PubMed (via PubTator3), and MyVariant.info to enable searching and retrieving information about clinical trials, research articles, and genetic variants. The server exposes these capabilities as MCP tools that can be used by AI assistants to access up-to-date biomedical data, overcoming knowledge cutoff limitations. BioMCP handles entity normalization, intelligent rendering of complex data as Markdown, and transparent attribution of sources, making it valuable for biomedical research, clinical decision support, and literature review workflows.
No reviews yet. Be the first to review!
Sign in to join the conversation
Highlight AISearch for articles by genes, diseases, variants, or keywords.
Get detailed article information including abstracts and full text.
Advanced trial search with filtering by condition, intervention, phase, etc.
Get detailed trial protocol information.
Retrieve trial site locations and contact information.
Get results and outcome measures from clinical trials.
Access related publications for clinical trials.
Search for genetic variants with sophisticated filtering.
Obtain comprehensive annotations from multiple sources (CIViC, ClinVar, COSMIC, dbSNP, etc.).
