PennCNV in whole-genome sequencing data

被引:0
|
作者
Leandro de Araújo Lima
Kai Wang
机构
[1] Zilkha Neurogenetic Institute,Department of Biomedical Informatics
[2] University of Southern California,undefined
[3] Present address: Gladstone Institute of Neurological Disease,undefined
[4] J. Gladstone Institutes,undefined
[5] Present address: Institute for Genomic Medicine,undefined
[6] Columbia University,undefined
[7] Columbia University,undefined
来源
关键词
Copy-number variation; Whole-genome sequencing; PennCNV;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [1] PennCNV in whole-genome sequencing data
    Lima, Leandro de Araujo
    Wang, Kai
    [J]. BMC BIOINFORMATICS, 2017, 18
  • [2] Whole-genome sequencing data of Kazakh individuals
    Kairov, Ulykbek
    Molkenov, Askhat
    Rakhimova, Saule
    Kozhamkulov, Ulan
    Sharip, Aigul
    Karabayev, Daniyar
    Daniyarov, Asset
    Lee, Joseph H.
    Terwilliger, Joseph D.
    Akilzhanova, Ainur
    Zhumadilov, Zhaxybay
    [J]. BMC RESEARCH NOTES, 2021, 14 (01)
  • [3] Whole-genome sequencing data of Kazakh individuals
    Ulykbek Kairov
    Askhat Molkenov
    Saule Rakhimova
    Ulan Kozhamkulov
    Aigul Sharip
    Daniyar Karabayev
    Asset Daniyarov
    Joseph H.Lee
    Joseph D.Terwilliger
    Ainur Akilzhanova
    Zhaxybay Zhumadilov
    [J]. BMC Research Notes, 14
  • [4] Whole-genome sequencing
    Morris, Huw R.
    Houlden, Henry
    Polke, James
    [J]. PRACTICAL NEUROLOGY, 2021, 21 (04) : 322 - +
  • [5] Saturation analysis for whole-genome bisulfite sequencing data
    Emanuele Libertini
    Simon C Heath
    Rifat A Hamoudi
    Marta Gut
    Michael J Ziller
    Javier Herrero
    Agata Czyz
    Victor Ruotti
    Hendrik G Stunnenberg
    Mattia Frontini
    Willem H Ouwehand
    Alexander Meissner
    Ivo G Gut
    Stephan Beck
    [J]. Nature Biotechnology, 2016, 34 : 691 - 693
  • [6] Discovering missing heritability in whole-genome sequencing data
    Alexander I. Young
    [J]. Nature Genetics, 2022, 54 : 224 - 226
  • [7] Saturation analysis for whole-genome bisulfite sequencing data
    Libertini, Emanuele
    Heath, Simon C.
    Hamoudi, Rifat A.
    Gut, Marta
    Ziller, Michael J.
    Herrero, Javier
    Czyz, Agata
    Ruotti, Victor
    Stunnenberg, Hendrik G.
    Frontini, Mattia
    Ouwehand, Willem H.
    Meissner, Alexander
    Gut, Ivo G.
    Beck, Stephan
    [J]. NATURE BIOTECHNOLOGY, 2016, 34 (07) : 691 - 693
  • [8] Discovering missing heritability in whole-genome sequencing data
    Young, Alexander, I
    [J]. NATURE GENETICS, 2022, 54 (03) : 224 - 226
  • [9] 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
  • [10] Whole-genome sequencing in pharmacogeneticson
    Urban, Thomas J.
    [J]. PHARMACOGENOMICS, 2013, 14 (04) : 345 - 348