"Testing subscribe functionality on a Python server" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Official STRING database MCP server. Query for protein-protein interactions, enrichment, annotations, homology, and PPI networks.
Sovereign intelligence dossiers, daily briefings, RAG search, knowledge graph, codon optimizer.
Due diligence on life-science claims: omics, trials, gene therapy. Dimension by dimension.
Look up allele frequencies by ancestry, gene constraint, variants, and coverage over gnomAD.
Collaborative BrAPI v2.1 MCP workspace — studies, germplasm, genotypes across Breedbase, T3, more.
Link compounds to protein targets, rank bioactivity, and look up drug mechanisms and indications.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.
Protein research over UniProtKB — search by function, fetch curated records, map IDs, proteomes.
Search GBIF species taxonomy, occurrence records, datasets, and publishers.
HLA nomenclature and match checks against a pinned IPD-IMGT/HLA release. No patient identifiers.
A unified biomedical graph database that integrates 50+ primary data sources — genes, proteins, compounds, diseases, pathways, and clinical data — into a single queryable graph with billions of cross-reference edges. Its native MCP server gives LLMs direct access to structured, authoritative biomedical data, complementing their reasoning with reliable identifiers and up-to-date database content.
PatSnap Biology Modality MCP server — access biological sequences, modification records, and antibody-antigen interactions across 200M+ patents.
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
Serves the user's personal DNA wellness report to their AI: caffeine response, sleep timing, training, nutrient absorption. Built from a hand-checked evidence base (GWAS Catalog, PharmGKB); every finding states its effect size and links to its source paper. No disease risk scores. The raw DNA file is parsed in the user's browser and never uploaded.
