OpenAlex | Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Work

Year: 2018

Type: article

Abstract: Copy number variation (CNV) analysis is an integral component of the study of human genomes in both research and clinical settings. Array-based CNV analysis is the current first-tier approach in clini... more

Source: Journal of Medical Genetics

Authors Bo Zhou, Steve S. Ho, Xianglong Zhang, Reenal Pattni, Rajini Haraksingh +1 more

Institutions Stanford University, University of the West Indies

Cites: 41

Cited by: 93

Related to: 10

FWCI: 9.266

Citation percentile (by year/subfield): 80.04

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

Sustainable Development Goal Industry, innovation and infrastructure

Open Access status: green

Funders School of Medicine, Stanford University, National Heart, Lung, and Blood Institute, National Human Genome Research Institute