"How to create documents in Confluence 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.
Official answers about Helena Bioinformatics and its products, with citations to public sources.
Look up allele frequencies by ancestry, gene constraint, variants, and coverage over gnomAD.
Link compounds to protein targets, rank bioactivity, and look up drug mechanisms and indications.
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.
Cancer gene co-occurrence and exclusivity in tumour cohorts, with confound controls and exact tests.
Search GBIF species taxonomy, occurrence records, datasets, and publishers.
Sovereign intelligence dossiers, daily briefings, RAG search, knowledge graph, codon optimizer.
Collaborative BrAPI v2.1 MCP workspace — studies, germplasm, genotypes across Breedbase, T3, more.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
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.
CIViC — Clinical Interpretation of Variants in Cancer.
PDBe (Protein Data Bank in Europe, EBI) MCP.
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.
