"Information or Uses for a Rag" 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.
Read-only MCP connector for The Dose Guy source-linked peptide and compound database. Search 260+ compounds, compare vendors and prices, inspect ranking evidence, and retrieve canonical page links. No authentication required.
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
Search biomedical papers, inspect publication records, and traverse citation or semantic graphs.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
Cited gene, variant (rsID) and CPIC drug–gene lookups for AI agents. Read-only, no key.
HLA nomenclature and match checks against a pinned IPD-IMGT/HLA release. No patient identifiers.
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
PubMed id shape, value discarded
Percent-triplet count, input discarded
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.
Biotech rNPV/PoS engine for AI agents. Signed exports, evidence register, asset landscape.
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
Public read-only MCP for the Y-chromosome haplogroup tree & Y-SNP resolution. 父系单倍群树查询与Y-SNP解析。
UCSC Genome Browser REST API — reference genome assemblies for ~250 species, the annotation tracks…
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.
