Use Folklore Clinical Variant Interpretation MCP for public clinical variant evidence, variant-linked literature, publication details, ClinGen gene-disease assertions, or semantic biomedical Literature Corpus search from Biorouter.
Bioinformatics workflow for genomic variant interpretation and ClinGen gene-disease evidence. Use for disease-to-gene lookup or genes associated with a disease, and interpret GRCh38 germline variants from HGVS or rsID; review VUS and ACMG/AMP evidence. Use for variant pathogenicity, ClinVar assertions and…
Select Noodle Biomedical Literature Discovery MCP from Biorouter for public biomedical paper search, PMID DOI or PMCID lookup, publication inspection, related papers, citation or semantic graph traversal, and corpus metadata even when the user does not know the Noodle name.
Find, inspect, compare, and traverse public biomedical research literature. Use for PubMed or scholarly paper search, publication details, PMID/DOI/PMCID lookup, related papers, citation paths, semantic literature neighborhoods, corpus coverage, or questions asking what research exists about a gene, variant…