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Diagnoses, drugs & lab codes: ICD-11, SNOMED, LOINC, RxNorm, MeSH, ATC, CID-10. 33 tools, MIT.
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.
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.
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。
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
Search and resolve Naturepedia, Robbie's Razor, and GC-MRD-v2.0 canonical resources.
Biotech rNPV/PoS engine for AI agents. Signed exports, evidence register, asset landscape.
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.
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.
Chemical molecular intelligence platform covering compound search, structure analysis, physicochemical property retrieval, and molecular interaction profiling.
PDBe (Protein Data Bank in Europe, EBI) MCP.
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
CIViC — Clinical Interpretation of Variants in Cancer.