Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly-Reference-Cited by-同舟云学术

Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly

Published:2011-08 Issue:8 Volume:29 Page:723-730
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Li Yingrui,Zheng Hancheng,Luo Ruibang,Wu Honglong,Zhu Hongmei,Li Ruiqiang,Cao Hongzhi,Wu Boxin,Huang Shujia,Shao Haojing,Ma Hanzhou,Zhang Fan,Feng Shuijian,Zhang Wei,Du Hongli,Tian Geng,Li Jingxiang,Zhang Xiuqing,Li Songgang,Bolund Lars,Kristiansen Karsten,de Smith Adam J,Blakemore Alexandra I F,Coin Lachlan J M,Yang Huanming,Wang Jian,Wang Jun

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.1904.pdf

Reference50 articles.

1. Lander, E.S. et al. Initial sequencing and analysis of the human genome. Nature 409, 860–921 (2001).

2. Venter, J.C. et al. The sequence of the human genome. Science 291, 1304–1351 (2001).

3. International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature 431, 931–945 (2004).

4. Hinds, D.A. et al. Whole-genome patterns of common DNA variation in three human populations. Science 307, 1072–1079 (2005).

5. Stefansson, H. et al. A common inversion under selection in Europeans. Nat. Genet. 37, 129–137 (2005).

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