Full clinical variant workup — gnomAD population frequency, ClinVar significance, protein domain impact, AlphaFold structure context, and PubMed literature
Compare a gene across multiple species — find orthologs, retrieve sequences, compute alignments, and summarize conservation
Druggability assessment — protein function, 3D structures, ligand-bound PDBs, binding sites, interaction network, disease associations, and literature
Functional analysis of a gene list — batch summaries, pathway mapping, protein interactions, tissue expression, and phenotype associations
Generate a comprehensive gene report by combining data from NCBI, Ensembl, UniProt, ClinVar, PDB, InterPro, STRING, and KEGG
Research session lab notebook — start, annotate, update, report, or check status
Search PubMed for relevant biomedical literature on a gene, variant, disease, or topic and produce a structured literature summary
Generate a pathway deep-dive report combining Reactome pathway data, member gene summaries, ClinVar variants, and PubMed literature