Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.

doi:10.1038/ng.555

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Article

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.

Nature genetics - 1 May 2010

Park Hansoo, Kim Jong-Il, Ju Young Seok, Gokcumen Omer, Mills Ryan E, Kim Sheehyun, Lee Seungbok, Suh Dongwhan, Hong Dongwan, Kang Hyunseok Peter, Yoo Yun Joo, Shin Jong-Yeon, Kim Hyun-Jin, Yavartanoo Maryam, Chang Young Wha, Ha Jung-Sook, Chong Wilson, Hwang Ga-Ram, Darvishi Katayoon, Kim Hyeran, Yang Song Ju, Yang Kap-Seok, Kim Hyungtae, Hurles Matthew E, Scherer Stephen W, Carter Nigel P, Tyler-Smith Chris, Lee Charles, Seo Jeong-Sun

Abstract excerpt

Copy number variants (CNVs) account for the majority of human genomic diversity in terms of base coverage. Here, we have developed and applied a new method to combine high-resolution array comparative genomic hybridization (CGH) data with whole-genome DNA sequencing data to obtain a comprehensive catalog of common CNVs in Asian individuals. The genomes of 30 individuals from three Asian populations (Korean,...

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PMID: 20364138
DOI: 10.1038/ng.555
PMCID: PMC3329635

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