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Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
Official STRING database MCP server. Query for protein-protein interactions, enrichment, annotations, homology, and PPI networks.
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.
Official answers about Helena Bioinformatics and its products, with citations to public sources.
Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
Cancer gene co-occurrence and exclusivity in tumour cohorts, with confound controls and exact tests.
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.
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.
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
PubTator 3 MCP — biomedical entity search, literature search with entity
Chemical molecular intelligence platform covering compound search, structure analysis, physicochemical property retrieval, and molecular interaction profiling.
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。
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer