"Gathering Context from an Ubuntu Server" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
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.
Look up allele frequencies by ancestry, gene constraint, variants, and coverage over gnomAD.
Search GBIF species taxonomy, occurrence records, datasets, and publishers.
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...
Query STRING interactions, enrichment, annotations, homology, and PPI networks.
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.
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
Gene expression experiments and the brain structure ontology from the Allen Institute's Brain…
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.
