Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases (Genome Medicine, 2023)

(untitled) - Pagnamenta, AT; Camps, C; Giacopuzzi, E; Taylor, JM; Hashim, M; Calpena, E; Kaisaki, PJ; Hashimoto, A; Yu, J; Sanders, E; Schwessinger, R; Hughes, JR; et al.