"Assistance with Cursor Development" matching MCP connectors:

Scientific plotting for bioinformatics with about 160 free modules. Anonymous access supported.

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.

PubTator 3 MCP — biomedical entity search, literature search with entity highlighting, and…

Annotate and classify human genetic variants with GeneBe (ACMG, gnomAD, ClinVar). Research use only.

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.

Cancer gene co-occurrence and exclusivity in tumour cohorts, with confound controls and exact tests.

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.

Search public biomedical datasets, measured results, papers, trials and drug evidence with sources.

Fold proteins, co-fold ligands with binding affinity, design binders and embed sequences.