The impact and origin of copy number variations in the Oryza species-Reference-Cited by-同舟云学术

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The impact and origin of copy number variations in the Oryza species

Published:2016-03-29 Issue:1 Volume:17 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Bai Zetao,Chen Jinfeng,Liao Yi,Wang Meijiao,Liu Rong,Ge Song,Wing Rod A.,Chen Mingsheng

Funder

the National Natural Science Foundation of China

the State Key Laboratory of Plant Genomics

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/s12864-016-2589-2

Reference101 articles.

1. Girirajan S, Campbell CD, Eichler EE. Human copy number variation and complex genetic disease. Annu Rev Genet. 2011;45:203–26.

2. Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C, et al. Mapping copy number variation by population-scale genome sequencing. Nature. 2011;470(7332):59–65.

3. Weischenfeldt J, Symmons O, Spitz F, Korbel JO. Phenotypic impact of genomic structural variation: insights from and for human disease. Nat Rev Genet. 2013;14(2):125–38.

4. Zhang F, Gu W, Hurles ME, Lupski JR. Copy number variation in human health, disease, and evolution. Annu Rev Genomics Hum Genet. 2009;10:451–81.

5. Iskow RC, Gokcumen O, Lee C. Exploring the role of copy number variants in human adaptation. Trends Genet. 2012;28(6):245–57.

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