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Official answers about Helena Bioinformatics and its products, with citations to public sources.
UniProt protein data: find proteins, map genes to proteins, function and disease links
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
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.
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
Gene expression experiments and the brain structure ontology from the Allen Institute's Brain…
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.
Educational insights from your lab results, DNA files and wearable data. EU-hosted, GDPR-first.
Auditable multi-agent topology generator from Drosophila MaleCNS connectome motifs.
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.
