compreheNGSive - A Visualization Tool for Prioritizing Variants from Next Generation Sequence Data

被引:0
|
作者
Bigelow, Alex [1 ]
Meyer, Miriah [1 ]
Camp, Nicola J. [1 ]
机构
[1] Univ Utah, Div Genet Epidemiol, Sci Comp & Imaging Inst, Salt Lake City, UT 84112 USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
50
引用
收藏
页码:734 / 734
页数:1
相关论文
共 50 条
  • [1] ArchTEx: accurate extraction and visualization of next-generation sequence data
    Lai, William K. M.
    Bard, Jonathan E.
    Buck, Michael J.
    BIOINFORMATICS, 2012, 28 (07) : 1021 - 1023
  • [2] Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data
    Carr, Ian M.
    Morgan, Joanne
    Watson, Christopher
    Melnik, Svitlana
    Diggle, Christine P.
    Logan, Clare V.
    Harrison, Sally M.
    Taylor, Graham R.
    Pena, Sergio D. J.
    Markham, Alexander F.
    Alkuraya, Fowzan S.
    Black, Graeme C. M.
    Ali, Manir
    Bonthron, David T.
    HUMAN MUTATION, 2013, 34 (07) : 945 - 952
  • [3] Visualization of next generation sequencing data
    An, Jiyuan
    Lai, John
    Wang, Chenwei
    Tevz, Gregor
    Lehman, Melanie L.
    Nelson, Colleen C.
    BJU INTERNATIONAL, 2015, 116 : 35 - 36
  • [4] pTuneos: prioritizing tumor neoantigens from next-generation sequencing data
    Chi Zhou
    Zhiting Wei
    Zhanbing Zhang
    Biyu Zhang
    Chenyu Zhu
    Ke Chen
    Guohui Chuai
    Sheng Qu
    Lu Xie
    Yong Gao
    Qi Liu
    Genome Medicine, 11
  • [5] pTuneos: prioritizing tumor neoantigens from next-generation sequencing data
    Zhou, Chi
    Wei, Zhiting
    Zhang, Zhanbing
    Zhang, Biyu
    Zhu, Chenyu
    Chen, Ke
    Chuai, Guohui
    Qu, Sheng
    Xie, Lu
    Gao, Yong
    Liu, Qi
    GENOME MEDICINE, 2019, 11 (01)
  • [6] VarB: a variation browsing and analysis tool for variants derived from next-generation sequencing data
    Preston, Mark D.
    Manske, Magnus
    Horner, Neil
    Assefa, Samuel
    Campino, Susana
    Auburn, Sarah
    Zongo, Issaka
    Ouedraogo, Jean-Bosco
    Nosten, Francois
    Anderson, Tim
    Clark, Taane G.
    BIOINFORMATICS, 2012, 28 (22) : 2983 - 2985
  • [7] Tablet-next generation sequence assembly visualization
    Milne, Iain
    Bayer, Micha
    Cardle, Linda
    Shaw, Paul
    Stephen, Gordon
    Wright, Frank
    Marshall, David
    BIOINFORMATICS, 2010, 26 (03) : 401 - 402
  • [8] Statistical Tests for Disease Association with Rare Variants in Next-generation Sequence Data
    Basu, Saonli
    Pan, Wei
    GENETIC EPIDEMIOLOGY, 2012, 36 (07) : 731 - 732
  • [9] PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data
    Zhang, Lu
    Zhang, Jing
    Yang, Jing
    Ying, Dingge
    Lau, Yu Lung
    Yang, Wanling
    BIOINFORMATICS, 2013, 29 (01) : 124 - 125
  • [10] Next generation tools for genomic data generation, distribution, and visualization
    Nix, David A.
    Di Sera, Tonya L.
    Dalley, Brian K.
    Milash, Brett A.
    Cundick, Robert M.
    Quinn, Kevin S.
    Courdy, Samir J.
    BMC BIOINFORMATICS, 2010, 11