Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
Sarah L. Stenton, Melanie O’Leary, Gabrielle Lemire, Grace E. VanNoy, Stephanie P. DiTroia, Vijay S. Ganesh, Emily Groopman, Emily O’Heir, Brian E. Mangilog, Ikeoluwa Osei‐Owusu, Lynn S. Pais, Jillian Serrano, Moriel Singer‐Berk, Ben Weisburd, Michael W. Wilson, , Anne O’Donnell‐Luria
The paper evaluates variant prioritization methods for rare disease diagnosis using data from the Rare Genomes Project, finding that top models identify causal variants in most solved families and uncover potential candidates in unsolved ones.
Human Genomics · Apr 29, 2024Peer-reviewedGenetic & Genomic Medicine