Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de...
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
About this item
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Author / Creator
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 and Wang, Jun
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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More information
Scope and Contents
Contents
Identification of genomic structural variation from short-read sequencing data is typically accomplished by mapping reads to a reference genome. Li
et al
. show that
de novo
assembly of the reads followed by whole-genome alignment to the reference is a more comprehensive method that can also resolve complex rearrangements.
Here we us...
Alternative Titles
Full title
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
Authors, Artists and Contributors
Author / Creator
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
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_893287309
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_893287309
Other Identifiers
ISSN
1087-0156,1546-1696
E-ISSN
1546-1696
DOI
10.1038/nbt.1904
