"A guide for reducing token count in AI requests" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Read-only MCP connector for The Dose Guy source-linked peptide and compound database. Search 260+ compounds, compare vendors and prices, inspect ranking evidence, and retrieve canonical page links. No authentication required.
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
Cited gene, variant (rsID) and CPIC drug–gene lookups for AI agents. Read-only, no key.
HLA nomenclature and match checks against a pinned IPD-IMGT/HLA release. No patient identifiers.
Public read-only MCP for the Y-chromosome haplogroup tree & Y-SNP resolution. 父系单倍群树查询与Y-SNP解析。
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
Hosted DNA language models: promoter, splice, enhancer, chromatin, expression, annotation
Percent-triplet count, input discarded
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.
Biotech rNPV/PoS engine for AI agents. Signed exports, evidence register, asset landscape.
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
PDBe (Protein Data Bank in Europe, EBI) MCP.
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
BioBricks: the site's own MCP server — dataset, enquiry (enquiry = a human handoff, not a...
UCSC Genome Browser REST API — reference genome assemblies for ~250 species, the annotation tracks…
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
CIViC — Clinical Interpretation of Variants in Cancer.
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.
Protein analysis: ESM-2/ESMC embeddings, mutation scoring, landscape scans, ESMFold structure.
