"How to interact with Ghost.org blogging platform" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Query STRING interactions, enrichment, annotations, homology, and PPI networks.
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.
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
Biomedical data: compounds, drug info, and molecular targets
Annotate and classify human genetic variants with GeneBe (ACMG, gnomAD, ClinVar). Research use only.
A molecular biology bench for AI assistants: cloning and assembly, PCR and primer design, CRISPR, Sanger verification, qPCR and dPCR, alignment and phylogenetics, genomics, proteins and cheminformatics. Calculated by engines checked against the field's reference tools, with every result explained. No auth, stateless, free.
Cancer gene co-occurrence and exclusivity in tumour cohorts, with confound controls and exact tests.
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
Deterministic peptide reconstitution and dosing math, so assistants compute it instead of guessing.
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.
PubTator 3 MCP — biomedical entity search, literature search with entity
Chemical molecular intelligence platform covering compound search, structure analysis, physicochemical property retrieval, and molecular interaction profiling.
MCP gateway federating 22 biomedical MCP servers behind one endpoint: gnomAD, ClinVar, HPO, VEP.
Fold proteins, co-fold ligands with binding affinity, design binders and embed sequences.
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.
