"Developing an application by analyzing specified development and API documentation" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
Query STRING interactions, enrichment, annotations, homology, and PPI networks.
Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
Due diligence on life-science claims: omics, trials, gene therapy. Dimension by dimension.
Sovereign intelligence dossiers, daily briefings, RAG search, knowledge graph, codon optimizer.
Run protein folding, docking, design and sequence analysis tools, and read their results.
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.
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.
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.
Resolve WoRMS marine species names; fetch classifications, synonyms, distributions, traits, and IDs.
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
Search InterPro entries, map domains onto proteins and PDB structures, and scan raw sequences.
Biomedical data: compounds, drug info, and molecular targets
Find pharmacogenomics guidelines, translate diplotypes, and retrieve prescribing recommendations.
Protein research over UniProtKB: search by function, fetch curated records, map IDs, proteomes.
Search GBIF species taxonomy, occurrence records, datasets, and publishers.
Agent research API for 15 disease areas, plus a T1D cure lab, sourced evidence ledger and models.
Annotate and classify human genetic variants with GeneBe (ACMG, gnomAD, ClinVar). Research use only.
