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
  • [31] GENE PREDICTION AND ANNOTATION IN PENSTEMON (PLANTAGINACEAE): A WORKFLOW FOR MARKER DEVELOPMENT FROM EXTREMELY LOW-COVERAGE GENOME SEQUENCING
    Blischak, Paul D.
    Wenzel, Aaron J.
    Wolfe, Andrea D.
    APPLICATIONS IN PLANT SCIENCES, 2014, 2 (12):
  • [32] Next-Generation Sequencing Data Analysis on Pool-Seq and Low-Coverage Retinoblastoma Data
    Ozdemir Ozdogan, Gulistan
    Kaya, Hilal
    INTERDISCIPLINARY SCIENCES-COMPUTATIONAL LIFE SCIENCES, 2020, 12 (03) : 302 - 310
  • [33] Next-Generation Sequencing Data Analysis on Pool-Seq and Low-Coverage Retinoblastoma Data
    Gülistan Özdemir Özdoğan
    Hilal Kaya
    Interdisciplinary Sciences: Computational Life Sciences, 2020, 12 : 302 - 310
  • [34] Phylogenomics from low-coverage whole-genome sequencing
    Zhang, Feng
    Ding, Yinhuan
    Zhu, Chao-Dong
    Zhou, Xin
    Orr, Michael C.
    Scheu, Stefan
    Luan, Yun-Xia
    METHODS IN ECOLOGY AND EVOLUTION, 2019, 10 (04): : 507 - 517
  • [35] Genomic prediction using low-coverage portable Nanopore sequencing
    Lamb, Harrison J.
    Hayes, Ben J.
    Randhawa, Imtiaz A. S.
    Nguyen, Loan T.
    Ross, Elizabeth M.
    PLOS ONE, 2021, 16 (12):
  • [36] Powerful eQTL mapping through low-coverage RNA sequencing
    Schwarz, Tommer
    Boltz, Toni
    Hou, Kangcheng
    Bot, Merel
    Duan, Chenda
    Loohuis, Loes Olde
    Boks, Marco P.
    Kahn, Rene S.
    Ophoff, Roel A.
    Pasaniuc, Bogdan
    HUMAN GENETICS AND GENOMICS ADVANCES, 2022, 3 (03):
  • [37] Low-Coverage Sequencing Imputation from millions of reference samples
    Rubinacci, Simone
    Delaneau, Olivier
    HUMAN HEREDITY, 2022, VOL. (SUPPL 1) : 4 - 5
  • [38] Rare Variant Association Testing Under Low-Coverage Sequencing
    Navon, Oron
    Sul, Jae Hoon
    Han, Buhm
    Conde, Lucia
    Bracci, Paige M.
    Riby, Jacques
    Skibola, Christine F.
    Eskin, Eleazar
    Halperin, Eran
    GENETICS, 2013, 194 (03): : 769 - +
  • [39] Linkage disequilibrium based genotype calling from low-coverage shotgun sequencing reads
    Duitama, Jorge
    Kennedy, Justin
    Dinakar, Sanjiv
    Hernandez, Yoezen
    Wu, Yufeng
    Mandoiu, Ion I.
    BMC BIOINFORMATICS, 2011, 12
  • [40] Detecting inherited and novel structural variants in low-coverage parent-child sequencing data
    Spence, Melissa
    Banuelos, Mario
    Marcia, Roummel F.
    Sindi, Suzanne
    METHODS, 2020, 173 : 61 - 68
12345