Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms-Reference-Cited by-同舟云学术

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms

Published:2015-06-01 Issue:1 Volume:6 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Abyzov Alexej,Li Shantao,Kim Daniel Rhee,Mohiyuddin Marghoob,Stütz Adrian M.,Parrish Nicholas F.^ORCID,Mu Xinmeng Jasmine,Clark Wyatt,Chen Ken,Hurles Matthew,Korbel Jan O.^ORCID,Lam Hugo Y. K.,Lee Charles,Gerstein Mark B.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms8256.pdf

Reference57 articles.

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3. Conrad, D. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704–712 (2009).

4. Stankiewicz, P. & Lupski, J. R. Structural variation in the human genome and its role in disease. Annu. Rev. Med. 61, 437–455 (2010).

5. Mefford, H. C. & Eichler, E. E. Duplication hotspots, rare genomic disorders, and common disease. Curr. Opin. Genet. Dev. 19, 196–204 (2009).

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