Work

ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies

Year: 2022

Type: article

Source: European Journal of Human Genetics

DOI: 10.1038/s41431-022-01222-7

Authors: Joseph T. Glessner, Jin Li, Yichuan Liu, Munir Khan, Xiao Chang, Patrick M. A. Sleiman, Hakon Hakonarson

Institutions: Children's Hospital of Philadelphia, Tianjin Medical University, University of Pennsylvania

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: U.S. Department of Health and Human Services, Medical Research Council, National Human Genome Research Institute

Awards: Integrative Analysis of a GWAS Repository with EMRs from over 40,000 Children, G3546651291, Utilizing Polygenic Risk to Understand and Improve Outcomes: A Model For Overturning Health Disparities Through Minority-Enriched Genomics Healthcare, G5850737185

OpenAlex ID: W4307744818

FWCI: 1.055

Cites: 27

Cited by: 10

Related to: 10