A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK Biobank

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Authors: Paras Garg, Bharati Jadhav, Mariya Shadrina, Alejandro Martin-Trujillo, Andrew J. Sharp
Cited by: 0
References: 60

Fields of Study & Subjects

Genetic Associations and Epidemiology Genomics and Rare Diseases RNA regulation and disease

Publication details

Journal / source
The American Journal of Human Genetics
Publisher
Elsevier BV
Volume
113
Issue
6
Pages
1297–1318
Publication date
20 May 2026
Language
EN