Mapping copy number variation by population-scale genome sequencing
Mapping copy number variation by population-scale genome sequencing
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Author / Creator
Mills, Ryan E. , Walter, Klaudia , Stewart, Chip , Handsaker, Robert E. , Chen, Ken , Alkan, Can , Abyzov, Alexej , Yoon, Seungtai Chris , Ye, Kai , Cheetham, R. Keira , Chinwalla, Asif , Conrad, Donald F. , Fu, Yutao , Grubert, Fabian , Hajirasouliha, Iman , Hormozdiari, Fereydoun , Iakoucheva, Lilia M. , Iqbal, Zamin , Kang, Shuli , Kidd, Jeffrey M. , Konkel, Miriam K. , Korn, Joshua , Khurana, Ekta , Kural, Deniz , Lam, Hugo Y. K. , Leng, Jing , Li, Ruiqiang , Li, Yingrui , Lin, Chang-Yun , Luo, Ruibang , Mu, Xinmeng Jasmine , Nemesh, James , Peckham, Heather E. , Rausch, Tobias , Scally, Aylwyn , Shi, Xinghua , Stromberg, Michael P. , Stütz, Adrian M. , Urban, Alexander Eckehart , Walker, Jerilyn A. , Wu, Jiantao , Zhang, Yujun , Zhang, Zhengdong D. , Batzer, Mark A. , Ding, Li , Marth, Gabor T. , McVean, Gil , Sebat, Jonathan , Snyder, Michael , Wang, Jun , Ye, Kenny , Eichler, Evan E. , Gerstein, Mark B. , Hurles, Matthew E. , Lee, Charles , McCarroll, Steven A. , Korbel, Jan O. and 1000 Genomes Project
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in extent, origin and functional impact. Despite progress in SV characterization, the nucleotide resolution architecture of most SVs remains unknown. We constructed a map of unbalanced SVs (that is, copy number variants) based on whole genome DNA seque...
Alternative Titles
Full title
Mapping copy number variation by population-scale genome sequencing
Authors, Artists and Contributors
Author / Creator
Walter, Klaudia
Stewart, Chip
Handsaker, Robert E.
Chen, Ken
Alkan, Can
Abyzov, Alexej
Yoon, Seungtai Chris
Ye, Kai
Cheetham, R. Keira
Chinwalla, Asif
Conrad, Donald F.
Fu, Yutao
Grubert, Fabian
Hajirasouliha, Iman
Hormozdiari, Fereydoun
Iakoucheva, Lilia M.
Iqbal, Zamin
Kang, Shuli
Kidd, Jeffrey M.
Konkel, Miriam K.
Korn, Joshua
Khurana, Ekta
Kural, Deniz
Lam, Hugo Y. K.
Leng, Jing
Li, Ruiqiang
Li, Yingrui
Lin, Chang-Yun
Luo, Ruibang
Mu, Xinmeng Jasmine
Nemesh, James
Peckham, Heather E.
Rausch, Tobias
Scally, Aylwyn
Shi, Xinghua
Stromberg, Michael P.
Stütz, Adrian M.
Urban, Alexander Eckehart
Walker, Jerilyn A.
Wu, Jiantao
Zhang, Yujun
Zhang, Zhengdong D.
Batzer, Mark A.
Ding, Li
Marth, Gabor T.
McVean, Gil
Sebat, Jonathan
Snyder, Michael
Wang, Jun
Ye, Kenny
Eichler, Evan E.
Gerstein, Mark B.
Hurles, Matthew E.
Lee, Charles
McCarroll, Steven A.
Korbel, Jan O.
1000 Genomes Project
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3077050
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3077050
Other Identifiers
ISSN
0028-0836
E-ISSN
1476-4687
DOI
10.1038/nature09708
