PhenoKG, a knowledge-graph-enhanced GNN and transformer model, achieves 24.64% MRR on the MyGene2 rare disease cohort versus 19.02% for SHEPHERD, and works without a candidate gene list.
Amelie speeds mendelian diagnosis by matching patient phenotype and genotype to primary literature
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PhenoKG: Knowledge Graph-Driven Gene Discovery and Patient Insights from Phenotypes Alone
PhenoKG, a knowledge-graph-enhanced GNN and transformer model, achieves 24.64% MRR on the MyGene2 rare disease cohort versus 19.02% for SHEPHERD, and works without a candidate gene list.