Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals-Reference-Cited by-同舟云学术

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

Published:2014-10-14 Issue:11 Volume:24 Page:1311-1327
ISSN:1001-0602
Container-title:Cell Research
language:en
Short-container-title:Cell Res

Author:

Huang August Y,Xu Xiaojing,Ye Adam Y,Wu Qixi,Yan Linlin,Zhao Boxun,Yang Xiaoxu,He Yao,Wang Sheng,Zhang Zheng,Gu Bowen,Zhao Han-Qing,Wang Meng,Gao Hua,Gao Ge,Zhang Zhichao,Yang Xiaoling,Wu Xiru,Zhang Yuehua,Wei Liping

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/cr2014131.pdf

Reference68 articles.

1. Lupski JR . Genome mosaicism — one human, multiple genomes. Science 2013; 341:358–359.

2. De S . Somatic mosaicism in healthy human tissues. Trends Genet 2011; 27:217–223.

3. Poduri A, Evrony GD, Cai X, Walsh CA . Somatic mutation, genomic variation, and neurological disease. Science 2013; 341:43.

4. Lawrence MS, Stojanov P, Polak P, et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature 2013; 499:214–218.

5. Nik-Zainal S, Alexandrov LB, Wedge DC, et al. Mutational processes molding the genomes of 21 breast cancers. Cell 2012; 149:979–993.

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