Kinship Estimation Based on Extremely Low-Coverage Sequencing Data

被引：0
|
作者：
Dou, Jinzhuang [1 ]
Chothani, Sonia [1 ]
Sim, Xueling [2 ]
Hughes, Jason D. [3 ]
Reilly, Dermot F. [3 ]
Tai, E. Shyong [2 ]
Liu, Jianjun [1 ]
Wang, Chaolong [1 ]
机构：
[1] Genome Inst Singapore, Singapore, Singapore
[2] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore, Singapore
[3] Merck Res Labs, Kenilworth, NJ USA
来源：
GENETIC EPIDEMIOLOGY | 2016年 / 40卷 / 07期
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：
31
引用
收藏
页码：619 / 620
页数：2
相关论文
共 50 条
  • [1] SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data
    Blischak, Paul D.
    Kubatko, Laura S.
    Wolfe, Andrea D.
    BIOINFORMATICS, 2018, 34 (03) : 407 - 415
  • [2] Optimisation of low-coverage sequencing approach
    Daviaud, Christian
    Gerber, Zuzana
    Meslage, Stephane
    Bacq-Daian, Dephine
    Meyer, Vincent
    Boland, Anne
    Deleuze, Jean-Francois
    Olaso, Robert
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 613 - 613
  • [3] Improved computations for relationship inference using low-coverage sequencing data
    Mostad, Petter
    Tillmar, Andreas
    Kling, Daniel
    BMC BIOINFORMATICS, 2023, 24 (01)
  • [4] Improved computations for relationship inference using low-coverage sequencing data
    Petter Mostad
    Andreas Tillmar
    Daniel Kling
    BMC Bioinformatics, 24
  • [5] ACE: absolute copy number estimation from low-coverage whole-genome sequencing data
    Poell, Jos B.
    Mendeville, Matias
    Sie, Daoud
    Brink, Arjen
    Brakenhoff, Ruud H.
    Ylstra, Bauke
    BIOINFORMATICS, 2019, 35 (16) : 2847 - 2849
  • [6] AKSmooth: Enhancing low-coverage bisulfite sequencing data via kernel-based smoothing
    Chen, Junfang
    Lutsik, Pavlo
    Akulenko, Ruslan
    Walter, Joern
    Helms, Volkhard
    JOURNAL OF BIOINFORMATICS AND COMPUTATIONAL BIOLOGY, 2014, 12 (06)
  • [7] Extremely low-coverage sequencing and imputation increases power for genome-wide association studies
    Bogdan Pasaniuc
    Nadin Rohland
    Paul J McLaren
    Kiran Garimella
    Noah Zaitlen
    Heng Li
    Namrata Gupta
    Benjamin M Neale
    Mark J Daly
    Pamela Sklar
    Patrick F Sullivan
    Sarah Bergen
    Jennifer L Moran
    Christina M Hultman
    Paul Lichtenstein
    Patrik Magnusson
    Shaun M Purcell
    David W Haas
    Liming Liang
    Shamil Sunyaev
    Nick Patterson
    Paul I W de Bakker
    David Reich
    Alkes L Price
    Nature Genetics, 2012, 44 : 631 - 635
  • [8] Extremely low-coverage whole genome sequencing in South Asians captures population genomics information
    Rustagi, Navin
    Zhou, Anbo
    Watkins, W. Scott
    Gedvilaite, Erika
    Wang, Shuoguo
    Ramesh, Naveen
    Muzny, Donna
    Gibbs, Richard A.
    Jorde, Lynn B.
    Yu, Fuli
    Xing, Jinchuan
    BMC GENOMICS, 2017, 18
  • [9] Extremely low-coverage whole genome sequencing in South Asians captures population genomics information
    Navin Rustagi
    Anbo Zhou
    W. Scott Watkins
    Erika Gedvilaite
    Shuoguo Wang
    Naveen Ramesh
    Donna Muzny
    Richard A. Gibbs
    Lynn B. Jorde
    Fuli Yu
    Jinchuan Xing
    BMC Genomics, 18
  • [10] Extremely low-coverage sequencing and imputation increases power for genome-wide association studies
    Pasaniuc, Bogdan
    Rohland, Nadin
    McLaren, Paul J.
    Garimella, Kiran
    Zaitlen, Noah
    Li, Heng
    Gupta, Namrata
    Neale, Benjamin M.
    Daly, Mark J.
    Sklar, Pamela
    Sullivan, Patrick F.
    Bergen, Sarah
    Moran, Jennifer L.
    Hultman, Christina M.
    Lichtenstein, Paul
    Magnusson, Patrik
    Purcell, Shaun M.
    Haas, David W.
    Liang, Liming
    Sunyaev, Shamil
    Patterson, Nick
    de Bakker, Paul I. W.
    Reich, David
    Price, Alkes L.
    NATURE GENETICS, 2012, 44 (06) : 631 - U41
12345