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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.
HLA nomenclature and match checks against a pinned IPD-IMGT/HLA release. No patient identifiers.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
Search and resolve Naturepedia, Robbie's Razor, and GC-MRD-v2.0 canonical resources.
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.
PatSnap Biology Modality MCP server — access biological sequences, modification records, and antibody-antigen interactions across 200M+ patents.
Gene expression experiments and the brain structure ontology from the Allen Institute's Brain…
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…
Serves the user's personal DNA wellness report to their AI: caffeine response, sleep timing, training, nutrient absorption. Built from a hand-checked evidence base (GWAS Catalog, PharmGKB); every finding states its effect size and links to its source paper. No disease risk scores. The raw DNA file is parsed in the user's browser and never uploaded.
