ALLELE-SPECIFIC COPY NUMBER ESTIMATION BY WHOLE EXOME SEQUENCING

被引:8
|
作者
Chen, Hao [1 ]
Jiang, Yuchao [2 ]
Maxwell, Kara N. [3 ]
Nathanson, Katherine L. [3 ]
Zhang, Nancy [2 ]
机构
[1] Univ Calif Davis, Dept Stat, One Shields Ave, Davis, CA 95616 USA
[2] Univ Penn, Wharton Sch, Dept Stat, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
来源
ANNALS OF APPLIED STATISTICS | 2017年 / 11卷 / 02期
关键词
Allele-specific copy number; whole exome sequencing; tumor-normal pair; CIRCULAR BINARY SEGMENTATION;
D O I
10.1214/17-AOAS1043
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Whole exome sequencing is currently a technology of choice in large-scale cancer genomics studies, where the priority is to identify cancer-associated variants in coding regions. We describe a method for estimating allele-specific copy number using whole exome sequencing data from tumor and matched normal.
引用
收藏
页码:1169 / 1192
页数:24
相关论文
共 50 条
  • [21] Assessment of genetic copy number variations yield in Whole exome sequencing
    Georgiev, Martin
    Kamenarova, Kunka
    Kachakova-Yordanova, Darina
    Ivanova, Neviana
    Beltcheva, Olga
    Mihova, Kalina
    Peycheva, Valentina
    Kaneva, Radka
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1169 - 1170
  • [22] VEGAWES: variational segmentation on whole exome sequencing for copy number detection
    Samreen Anjum
    Sandro Morganella
    Fulvio D’Angelo
    Antonio Iavarone
    Michele Ceccarelli
    BMC Bioinformatics, 16
  • [23] Sacral agenesis: a pilot whole exome sequencing and copy number study
    Porsch, Robert M.
    Merello, Elisa
    De Marco, Patrizia
    Cheng, Guo
    Rodriguez, Laura
    So, Manting
    Sham, Pak C.
    Tam, Paul K.
    Capra, Valeria
    Cherny, Stacey S.
    Garcia-Barcelo, Maria-Merce
    Campbell, Desmond D.
    BMC MEDICAL GENETICS, 2016, 17
  • [24] Accurate total and allele-specific copy number measurements in mosaic tumors
    Curry, Bo
    Sampas, Nick
    Anderson, Paige
    Peters, Brian
    CANCER RESEARCH, 2011, 71
  • [25] Allele-specific multi-sample copy number segmentation in ASCAT
    Ross, Edith M.
    Haase, Kerstin
    Van Loo, Peter
    Markowetz, Florian
    BIOINFORMATICS, 2021, 37 (13) : 1909 - 1911
  • [26] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing
    Shen, Ronglai
    Seshan, Venkatraman E.
    NUCLEIC ACIDS RESEARCH, 2016, 44 (16)
  • [27] Tumor-Only Allele-Specific Copy Number Calling with a Targeted Next-Generation Sequencing Panel
    Hadjis, A.
    Patterson, T.
    Rogers, M.
    Johnson, L.
    Fridey, T.
    McConnell, D.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2024, 26 (11): : S85 - S86
  • [28] Probe-free allele-specific copy number detection and analysis of tumors
    Zhu, Ailin
    Guan, Xiaowei
    Gu, Xinbin
    Xie, Guiqin
    ANALYTICAL BIOCHEMISTRY, 2016, 497 : 95 - 102
  • [29] ECOLE: Learning to call copy number variants on whole exome sequencing data
    Mandiracioglu, Berk
    Ozden, Furkan
    Kaynar, Gun
    Yilmaz, Mehmet Alper
    Alkan, Can
    Cicek, A. Ercument
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [30] inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing
    Chanwigoon, Saowwapark
    Piwluang, Sakkayaphab
    Wichadakul, Duangdao
    EVOLUTIONARY BIOINFORMATICS, 2020, 16