"Reading terminal outputs from a Next.js dev server while developing in Cursor" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.
CIViC — Clinical Interpretation of Variants in Cancer.
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
Gene expression experiments and the brain structure ontology from the Allen Institute's Brain…
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.
Agent research API for 15 disease areas, plus a T1D cure lab, sourced evidence ledger and models.
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...
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
HLA nomenclature and match checks against a pinned IPD-IMGT/HLA release. No patient identifiers.
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.
PubMed id shape, value discarded
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
Percent-triplet count, input discarded
PDBe (Protein Data Bank in Europe, EBI) MCP.
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
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.
