Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly-Reference-Cited by-同舟云学术

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Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly

Published:2012-07-15 Issue:8 Volume:30 Page:771-776
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Lam Ernest T,Hastie Alex,Lin Chin,Ehrlich Dean,Das Somes K,Austin Michael D,Deshpande Paru,Cao Han,Nagarajan Niranjan,Xiao Ming,Kwok Pui-Yan

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/nbt.2303.pdf

Reference38 articles.

1. Ley, T.J. et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 456, 66–72 (2008).

2. Li, R. et al. De novo assembly of human genomes with massively parallel short read sequencing. Genome Res. 20, 265–272 (2010).

3. Fernando, M.M.A. et al. Defining the role of the MHC in autoimmunity: a review and pooled analysis. PLoS Genet. 4, e1000024 (2008).

4. Sebat, J. et al. Large-scale copy number polymorphism in the human genome. Science 305, 525–528 (2004).

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

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