"Guidelines for Managing File Structures" 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.
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.
Search InterPro entries, map domains onto proteins and PDB structures, and scan raw sequences.
Find pharmacogenomics guidelines, translate diplotypes, and retrieve prescribing recommendations.
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
AlphaFold DB MCP — predicted protein structures.
Agent research API for 15 disease areas, plus a T1D cure lab, sourced evidence ledger and models.
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.
RCSB PDB MCP — experimentally determined macromolecular structures.
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
Biotech rNPV/PoS engine for AI agents. Signed exports, evidence register, asset landscape.
UCSC Genome Browser REST API — reference genome assemblies for ~250 species, the annotation tracks…
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
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。
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
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.
AI orchestration for computational chemistry and HPC workflows.
