"A database of diseases with associated genetic variants and sequencing information" matching MCP connectors:
GET /v1/connectors — MCP directory API referenceMatching Connector Tools:
Helena Bioinformatics MCP for clinical variant interpretation, ACMG/AMP evidence and literature.
Deterministic peptide reconstitution and dosing math, so assistants compute it instead of guessing.
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
Look up allele frequencies by ancestry, gene constraint, variants, and coverage over gnomAD.
Link compounds to protein targets, rank bioactivity, and look up drug mechanisms and indications.
Search GBIF species taxonomy, occurrence records, datasets, and publishers.
Search biomedical papers, inspect publication records, and traverse citation or semantic graphs.
Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.
Official answers about Helena Bioinformatics and its products, with citations to public sources.
Monarch biomedical knowledge graph — diseases, phenotypes, genes, variants
GWAS Catalog (EBI/NHGRI) MCP — curated catalog of genome-wide association studies.
PomBase MCP — the fission yeast (Schizosaccharomyces pombe) model-organism database.
UniProt MCP — protein sequence + function database.
Bioregistry — meta-registry of biomedical identifier prefixes
Search and resolve Naturepedia, Robbie's Razor, and GC-MRD-v2.0 canonical resources.
ChEMBL MCP — drug discovery database (EBI).
WikiPathways MCP — open community pathway database.
Broad Institute gnomAD genomic variant database (GraphQL)
Query STRING interactions, enrichment, annotations, homology, and PPI networks.
Reactome biological pathway database
