"Tools to generate Lucidchart diagrams from Java code" matching MCP connectors:

Diagnoses, drugs & lab codes: ICD-11, LOINC, RxNorm, MeSH, ATC, CID-10. 33 tools, MIT.

Run protein folding, docking, design and sequence analysis tools, and read their results.

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.

Look up genes, sequences, variants, homologs, and cross-database xrefs from Ensembl REST.

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…

Validated molecular biology tools: cloning, primers, CRISPR, Sanger, alignment, qPCR, phylogenetics

Find open biology and chemistry AI models, bioinformatics tools and databases, and run them online.

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.

PK serum simulation, reconstitution math and compound data for agents. Paid tools $0.01 via x402.

BioBTreeA

bio.sugi

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.

dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…

Hosted DNA/RNA/protein tools: primers, oligos, PCR, cloning, CRISPR, alignment, batch & pipelines.

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.