Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing-Reference-Cited by-同舟云学术

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

Published:2010-04-04 Issue:5 Volume:42 Page:400-405
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.555.pdf

Reference23 articles.

1. Iafrate, A.J. et al. Detection of large-scale variation in the human genome. Nat. Genet. 36, 949–951 (2004).

2. Conrad, D.F. et al. Origins and functional impact of copy number variation in the human genome. Nature advance online publication, doi:10.1038/nature08516 (7 October 2009).

3. Perry, G.H. et al. The fine-scale and complex architecture of human copy-number variation. Am. J. Hum. Genet. 82, 685–695 (2008).

4. Redon, R. et al. Global variation in copy number in the human genome. Nature 444, 444–454 (2006).

5. Kim, J.I. et al. A highly annotated whole-genome sequence of a Korean individual. Nature 460, 1011–1015 (2009).

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