Identifying insertion mutations by whole-genome sequencing

被引:11
|
作者
Smith, Harold E. [1 ]
机构
[1] NIDDKD, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Next-generation sequencing; whole-genome resequencing; mutation identification; insertion mapping; ESCHERICHIA-COLI;
D O I
10.2144/000113600
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Insertion mutagenesis via mobile genetic element is a common technique for the analysis of gene function in model organisms. Next-generation sequencing offers an attractive approach for localizing the site of insertion, but alignment-based mapping of mobile genetic elements is challenging. A computational method for identifying insertion sites is reported herein. The technique was validated by mapping transposons in both bacterial and nematode species. The approach should be extensible to other systems that employ mobile genetic elements to generate mutations.
引用
收藏
页码:96 / 97
页数:2
相关论文
共 50 条
  • [1] Using whole-genome sequencing to discover mutations
    Laffman-Johnson, Elise
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 85 (02) : 118 - 118
  • [2] Whole-genome sequencing identifies Mendelian mutations
    Meera Swami
    [J]. Nature Reviews Genetics, 2010, 11 : 313 - 313
  • [3] Mapping Challenging Mutations by Whole-Genome Sequencing Aimee
    Smith, Harold E.
    Fabritius, Amy S.
    Jaramillo-Lambert, Aimee
    Golden, Andy
    [J]. G3-GENES GENOMES GENETICS, 2016, 6 (05): : 1297 - 1304
  • [4] Use of a Sibling Subtraction Method for Identifying Causal Mutations in Caenorhabditis elegans by Whole-Genome Sequencing
    Joseph, Braveen B.
    Blouin, Nicolas A.
    Fay, David S.
    [J]. G3-GENES GENOMES GENETICS, 2018, 8 (02): : 669 - 678
  • [5] Whole-genome sequencing
    Morris, Huw R.
    Houlden, Henry
    Polke, James
    [J]. PRACTICAL NEUROLOGY, 2021, 21 (04) : 322 - +
  • [6] Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma
    Kan, Zhengyan
    Zheng, Hancheng
    Liu, Xiao
    Li, Shuyu
    Barber, Thomas D.
    Gong, Zhuolin
    Gao, Huan
    Hao, Ke
    Willard, Melinda D.
    Xu, Jiangchun
    Hauptschein, Robert
    Rejto, Paul A.
    Fernandez, Julio
    Wang, Guan
    Zhang, Qinghui
    Wang, Bo
    Chen, Ronghua
    Wang, Jian
    Lee, Nikki P.
    Zhou, Wei
    Lin, Zhao
    Peng, Zhiyu
    Yi, Kang
    Chen, Shengpei
    Li, Lin
    Fan, Xiaomei
    Yang, Jie
    Ye, Rui
    Ju, Jia
    Wang, Kai
    Estrella, Heather
    Deng, Shibing
    Wei, Ping
    Qiu, Ming
    Wulur, Isabella H.
    Liu, Jiangang
    Ehsani, Mariam E.
    Zhang, Chunsheng
    Loboda, Andrey
    Sung, Wing Kin
    Aggarwal, Amit
    Poon, Ronnie T.
    Fan, Sheung Tat
    Wang, Jun
    Hardwick, James
    Reinhard, Christoph
    Dai, Hongyue
    Li, Yingrui
    Luk, John M.
    Mao, Mao
    [J]. GENOME RESEARCH, 2013, 23 (09) : 1422 - 1433
  • [7] DISEASE GENETICS Whole-genome sequencing identifies Mendelian mutations
    Swami, Meera
    [J]. NATURE REVIEWS GENETICS, 2010, 11 (05) : 313 - 313
  • [8] Whole-genome sequencing reveals oncogenic mutations in mycosis fungoides
    McGirt, Laura Y.
    Jia, Peilin
    Baerenwald, Devin A.
    Duszynski, Robert J.
    Dahlman, Kimberly B.
    Zic, John A.
    Zwerner, Jeffrey P.
    Hucks, Donald
    Dave, Utpal
    Zhao, Zhongming
    Eischen, Christine M.
    [J]. BLOOD, 2015, 126 (04) : 508 - 519
  • [9] A Strategy for Direct Mapping and Identification of Mutations by Whole-Genome Sequencing
    Zuryn, Steven
    Le Gras, Stephanie
    Jamet, Karine
    Jarriault, Sophie
    [J]. GENETICS, 2010, 186 (01) : 427 - 430
  • [10] Interpreting Whole-Genome Sequencing
    Grody, Wayne W.
    Vilain, Eric
    Nelson, Stanley F.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2014, 312 (03): : 296 - 296