"Tools for Creating Tasks Without Needing an API Key" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Diagnoses, drugs & lab codes: ICD-11, LOINC, RxNorm, MeSH, ATC, CID-10. 33 tools, MIT.
Official STRING database MCP server. Query for protein-protein interactions, enrichment, annotations, homology, and PPI networks.
Run protein folding, docking, design and sequence analysis tools, and read their results.
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.
Due diligence on life-science claims: omics, trials, gene therapy. Dimension by dimension.
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
Search biomedical papers, inspect publication records, and traverse citation or semantic graphs.
Official answers about Helena Bioinformatics and its products, with citations to public sources.
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.
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。
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
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…
DrugBank MCP — wraps the DrugBank Clinical API (api.drugbank.com)
UMLS MCP — wraps the NLM UMLS Terminology Services REST API (uts-ws.nlm.nih.gov/rest)
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
