High-Resolution Detection of Identity by Descent in Unrelated Individuals

被引:164
作者
Browning, Sharon R. [1 ]
Browning, Brian L. [1 ]
机构
[1] Univ Auckland, Dept Stat, Auckland 1, New Zealand
基金
英国惠康基金; 美国国家卫生研究院;
关键词
WHOLE-GENOME ASSOCIATION; EXTENDED PEDIGREES; WIDE ASSOCIATION; HOMOZYGOSITY; SEGMENTS; MODEL;
D O I
10.1016/j.ajhg.2010.02.021
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Detection of recent identity by descent (IBD) in population samples is important for population-based linkage mapping and for highly accurate genotype imputation and haplotype-phase inference. We present a method for detection of recent IBD in population samples. Our method accounts for linkage disequilibrium between SNPs to enable full use of high-density SNP data. We find that our method can detect segments of a length of 2 cM with moderate power and negligible false discovery rate in II lumina 550K data in Northwestern Europeans. We compare our method with GERMLINE and PUNK, and we show that our method has a level of resolution that is significantly better than these existing methods, thus extending the usefulness of recent IBD in analysis of high-density SNP data. We survey four genomic regions in a sample of UK individuals of European descent and find that on average, at a given location, our method detects IBD in 2.7 per 10,000 pairs of individuals in II lumina 550K data. We also present methodology and results for detection of homozygosity by descent (HBD) and survey the whole genome in a sample of 1373 UK individuals of European descent. We detect HBD in 4.7 individuals per 10,000 on average at a given location. Our methodology is implemented in the freely available BEAGLE software package.
引用
收藏
页码:526 / 539
页数:14
相关论文
共 29 条
[1]   Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: Fasting serum-insulin level in the hutterites [J].
Abney, M ;
Ober, C ;
McPeek, MS .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (04) :920-934
[2]   Relatedness Mapping and Tracts of Relatedness for Genome-Wide Data in the Presence of Linkage Disequilibrium [J].
Albrechtsen, Anders ;
Korneliussen, Thorfinn Sand ;
Moltke, Ida ;
Hansen, Thomas van Overseem ;
Nielsen, Finn Cilius ;
Nielsen, Rasmus .
GENETIC EPIDEMIOLOGY, 2009, 33 (03) :266-274
[3]  
Baum L.E., 1972, P 3 S INE, P1
[4]   Simultaneous Genotype Calling and Haplotype Phasing Improves Genotype Accuracy and Reduces False-Positive Associations for Genome-wide Association Studies [J].
Browning, Brian L. ;
Yu, Zhaoxia .
AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 85 (06) :847-861
[5]   Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes [J].
Browning, Sharon R. .
GENETICS, 2008, 178 (04) :2123-2132
[6]   Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering [J].
Browning, Sharon R. ;
Browning, Brian L. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (05) :1084-1097
[7]   Multilocus association mapping using variable-length Markov chains [J].
Browning, Sharon R. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 78 (06) :903-913
[8]   Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].
Burton, Paul R. ;
Clayton, David G. ;
Cardon, Lon R. ;
Craddock, Nick ;
Deloukas, Panos ;
Duncanson, Audrey ;
Kwiatkowski, Dominic P. ;
McCarthy, Mark I. ;
Ouwehand, Willem H. ;
Samani, Nilesh J. ;
Todd, John A. ;
Donnelly, Peter ;
Barrett, Jeffrey C. ;
Davison, Dan ;
Easton, Doug ;
Evans, David ;
Leung, Hin-Tak ;
Marchini, Jonathan L. ;
Morris, Andrew P. ;
Spencer, Chris C. A. ;
Tobin, Martin D. ;
Attwood, Antony P. ;
Boorman, James P. ;
Cant, Barbara ;
Everson, Ursula ;
Hussey, Judith M. ;
Jolley, Jennifer D. ;
Knight, Alexandra S. ;
Koch, Kerstin ;
Meech, Elizabeth ;
Nutland, Sarah ;
Prowse, Christopher V. ;
Stevens, Helen E. ;
Taylor, Niall C. ;
Walters, Graham R. ;
Walker, Neil M. ;
Watkins, Nicholas A. ;
Winzer, Thilo ;
Jones, Richard W. ;
McArdle, Wendy L. ;
Ring, Susan M. ;
Strachan, David P. ;
Pembrey, Marcus ;
Breen, Gerome ;
St Clair, David ;
Caesar, Sian ;
Gordon-Smith, Katherine ;
Jones, Lisa ;
Fraser, Christine ;
Green, Elain K. .
NATURE, 2007, 447 (7145) :661-678
[9]   A second generation human haplotype map of over 3.1 million SNPs [J].
Frazer, Kelly A. ;
Ballinger, Dennis G. ;
Cox, David R. ;
Hinds, David A. ;
Stuve, Laura L. ;
Gibbs, Richard A. ;
Belmont, John W. ;
Boudreau, Andrew ;
Hardenbol, Paul ;
Leal, Suzanne M. ;
Pasternak, Shiran ;
Wheeler, David A. ;
Willis, Thomas D. ;
Yu, Fuli ;
Yang, Huanming ;
Zeng, Changqing ;
Gao, Yang ;
Hu, Haoran ;
Hu, Weitao ;
Li, Chaohua ;
Lin, Wei ;
Liu, Siqi ;
Pan, Hao ;
Tang, Xiaoli ;
Wang, Jian ;
Wang, Wei ;
Yu, Jun ;
Zhang, Bo ;
Zhang, Qingrun ;
Zhao, Hongbin ;
Zhao, Hui ;
Zhou, Jun ;
Gabriel, Stacey B. ;
Barry, Rachel ;
Blumenstiel, Brendan ;
Camargo, Amy ;
Defelice, Matthew ;
Faggart, Maura ;
Goyette, Mary ;
Gupta, Supriya ;
Moore, Jamie ;
Nguyen, Huy ;
Onofrio, Robert C. ;
Parkin, Melissa ;
Roy, Jessica ;
Stahl, Erich ;
Winchester, Ellen ;
Ziaugra, Liuda ;
Altshuler, David ;
Shen, Yan .
NATURE, 2007, 449 (7164) :851-U3
[10]   Whole population, genome-wide mapping of hidden relatedness [J].
Gusev, Alexander ;
Lowe, Jennifer K. ;
Stoffel, Markus ;
Daly, Mark J. ;
Altshuler, David ;
Breslow, Jan L. ;
Friedman, Jeffrey M. ;
Pe'er, Itsik .
GENOME RESEARCH, 2009, 19 (02) :318-326