"Assistance with Generating Code for Graph Visualization" matching MCP connectors:
GET /v1/connectors – MCP directory API referenceMatching Connector Tools:
Scientific plotting for bioinformatics with about 160 free modules. Anonymous access supported.
Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
Sovereign intelligence dossiers, daily briefings, RAG search, knowledge graph, codon optimizer.
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.
Official answers about Helena Bioinformatics and its products, with citations to public sources.
Ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, with ClinVar.
Annotate and classify human genetic variants with GeneBe (ACMG, gnomAD, ClinVar). Research use only.
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.
PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.
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.
Biotech intelligence for AI agents: drugs, targets, diagnostics, PoS estimates, and writeups.
UCSC Genome Browser REST API — reference genome assemblies for ~250 species, the annotation tracks…
PubTator 3 MCP — biomedical entity search, literature search with entity highlighting, and…
g:Profiler (University of Tartu) — functional enrichment analysis for a gene list against GO…
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
Monarch Initiative MCP — biomedical knowledge graph.
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
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.
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。
Search public biomedical datasets, measured results, papers, trials and drug evidence with sources.
GPU-accelerated compute engine for BioTuring's biological databases
Fold proteins, co-fold ligands with binding affinity, design binders and embed sequences.
AI orchestration for computational chemistry and HPC workflows.
