Sequencing and automated whole-genome optical mapping of the genome of a domestic goat (Capra hircus)

Yang Dong(Kunming Institute of Zoology), Min Xie(BGI Group (China)), Yu Jiang(Kunming Institute of Zoology), Nianqing Xiao(OpGen (United States)), Xiaoyong Du(Huazhong Agricultural University), Wenguang Zhang(Chinese Academy of Sciences), Gwenola Tosser‐Klopp(Laboratoire de Génétique Cellulaire), Jinhuan Wang(BGI Group (China)), Shuang Yang(BGI Group (China)), Jie Liang(BGI Group (China)), Wenbin Chen(BGI Group (China)), Jing Chen(BGI Group (China)), Peng Zeng(BGI Group (China)), Yong Hou(BGI Group (China)), Chao Bian(BGI Group (China)), Shengkai Pan(BGI Group (China)), Yuxiang Li(BGI Group (China)), Xin Liu(BGI Group (China)), Wenliang Wang(Chinese Academy of Sciences), Bertrand Servin(Laboratoire de Génétique Cellulaire), Brian L Sayre(Virginia State University), Bin Zhu(OpGen (United States)), Deacon Sweeney(OpGen (United States)), Rich Moore(OpGen (United States)), Wenhui Nie(Kunming Institute of Zoology), Yongyi Shen(Chinese Academy of Sciences), Ruoping Zhao(Kunming Institute of Zoology), Guojie Zhang(BGI Group (China)), Jinquan Li(Inner Mongolia Agricultural University), Thomas Faraut(Laboratoire de Génétique Cellulaire), James E. Womack(Texas A&M University), Ya‐Ping Zhang(Kunming Institute of Zoology), James Kijas(Commonwealth Scientific and Industrial Research Organisation), Noelle E. Cockett(Utah State University), Xun Xu(Kunming Institute of Zoology), Shuhong Zhao(Huazhong Agricultural University), Jun Wang(Chinese Academy of Sciences), Wen Wang(BGI Group (China))
Nature Biotechnology
December 23, 2012
Cited by 544Open Access
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Abstract

We report the ∼2.66-Gb genome sequence of a female Yunnan black goat. The sequence was obtained by combining short-read sequencing data and optical mapping data from a high-throughput whole-genome mapping instrument. The whole-genome mapping data facilitated the assembly of super-scaffolds >5× longer by the N50 metric than scaffolds augmented by fosmid end sequencing (scaffold N50 = 3.06 Mb, super-scaffold N50 = 16.3 Mb). Super-scaffolds are anchored on chromosomes based on conserved synteny with cattle, and the assembly is well supported by two radiation hybrid maps of chromosome 1. We annotate 22,175 protein-coding genes, most of which were recovered in the RNA-seq data of ten tissues. Comparative transcriptomic analysis of the primary and secondary follicles of a cashmere goat reveal 51 genes that are differentially expressed between the two types of hair follicles. This study, whose results will facilitate goat genomics, shows that whole-genome mapping technology can be used for the de novo assembly of large genomes.


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