Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.
Babadi M, Fu JM, Lee SK, Smirnov AN, Gauthier LD, Walker M, Benjamin DI, Zhao X, Karczewski KJ, Wong I, Collins RL, Sanchis-Juan A, Brand H, Banks E, Talkowski ME.
Babadi M, et al. Among authors: smirnov an.
Nat Genet. 2024 Mar;56(3):553. doi: 10.1038/s41588-024-01663-4.
Nat Genet. 2024.
PMID: 38263447
No abstract available.