High-resolution mapping of copy-number alterations with massively parallel sequencing-Reference-Cited by-同舟云学术

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High-resolution mapping of copy-number alterations with massively parallel sequencing

Published:2008-11-30 Issue:1 Volume:6 Page:99-103
ISSN:1548-7091
Container-title:Nature Methods
language:en
Short-container-title:Nat Methods

Author:

Chiang Derek Y,Getz Gad,Jaffe David B,O'Kelly Michael J T,Zhao Xiaojun,Carter Scott L,Russ Carsten,Nusbaum Chad,Meyerson Matthew,Lander Eric S

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Biochemistry,Biotechnology

Link

http://www.nature.com/articles/nmeth.1276.pdf

Reference28 articles.

1. Freeman, J.L. et al. Copy number variation: new insights in genome diversity. Genome Res. 16, 949–961 (2006).

2. McCarroll, S.A. & Altshuler, D.M. Copy-number variation and association studies of human disease. Nat. Genet. 39, S37–S42 (2007).

3. Beckmann, J.S., Estivill, X. & Antonarakis, S.E. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability. Nat. Rev. Genet. 8, 639–646 (2007).

4. Beroukhim, R. et al. Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma. Proc. Natl. Acad. Sci. USA 104, 20007–20012 (2007).

5. Pinkel, D. & Albertson, D.G. Array comparative genomic hybridization and its applications in cancer. Nat. Genet. 37, S11–S17 (2005).

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