Improving the Accuracy and Efficiency of Identity-by-Descent Detection in Population Data

被引:461
作者
Browning, Brian L. [1 ]
Browning, Sharon R. [2 ]
机构
[1] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
来源
GENETICS | 2013年 / 194卷 / 02期
基金
英国惠康基金; 美国国家卫生研究院;
关键词
WHOLE-GENOME ASSOCIATION; GENOTYPE DATA; LINKAGE DISEQUILIBRIUM; POSITIVE SELECTION; BIRTH COHORT; VARIANTS; HERITABILITY; INDIVIDUALS; HAPLOTYPES; IMPUTATION;
D O I
10.1534/genetics.113.150029
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Segments of indentity-by-descent (IBD) detected from high-density genetic data are useful for many applications, including long-range phase determination, phasing family data, imputation, IBD mapping, and heritability analysis in founder populations. We present Refined IBD, a new method for IBD segment detection. Refined IBD achieves both computational efficiency and highly accurate IBD segment reporting by searching for IBD in two steps. The first step (identification) uses the GERMLINE algorithm to find shared haplotypes exceeding a length threshold. The second step (refinement) evaluates candidate segments with a probabilistic approach to assess the evidence for IBD. Like GERMLINE, Refined IBD allows for IBD reporting on a haplotype level, which facilitates determination of multi-individual IBD and allows for haplotype-based downstream analyses. To investigate the properties of Refined IBD, we simulate SNP data from a model with recent superexponential population growth that is designed to match United Kingdom data. The simulation results show that Refined IBD achieves a better power/accuracy profile than fastIBD or GERMLINE. We find that a single run of Refined IBD achieves greater power than 10 runs of fastIBD. We also apply Refined IBD to SNP data for samples from the United Kingdom and from Northern Finland and describe the IBD sharing in these data sets. Refined IBD is powerful, highly accurate, and easy to use and is implemented in Beagle version 4.
引用
收藏
页码:459 / +
页数:16
相关论文
共 44 条
[11]   Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort [J].
Browning, Sharon R. ;
Browning, Brian L. .
HUMAN GENETICS, 2013, 132 (02) :129-138
[12]   Identity by Descent Between Distant Relatives: Detection and Applications [J].
Browning, Sharon R. ;
Browning, Brian L. .
ANNUAL REVIEW OF GENETICS, VOL 46, 2012, 46 :617-633
[13]   Detecting Rare Variant Associations by Identity-by-Descent Mapping in Case-Control Studies [J].
Browning, Sharon R. ;
Thompson, Elizabeth A. .
GENETICS, 2012, 190 (04) :1521-1531
[14]   Haplotype phasing: existing methods and new developments [J].
Browning, Sharon R. ;
Browning, Brian L. .
NATURE REVIEWS GENETICS, 2011, 12 (10) :703-714
[15]   High-Resolution Detection of Identity by Descent in Unrelated Individuals [J].
Browning, Sharon R. ;
Browning, Brian L. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (04) :526-539
[16]   Identification of regions of positive selection using Shared Genomic Segment analysis [J].
Cai, Zheng ;
Camp, Nicola J. ;
Cannon-Albright, Lisa ;
Thomas, Alun .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (06) :667-671
[17]   North African Jewish and non-Jewish populations form distinctive, orthogonal clusters [J].
Campbell, Christopher L. ;
Palamara, Pier F. ;
Dubrovsky, Maya ;
Botigue, Laura R. ;
Fellous, Marc ;
Atzmon, Gil ;
Oddoux, Carole ;
Pearlman, Alexander ;
Hao, Li ;
Henn, Brenna M. ;
Burns, Edward ;
Bustamante, Carlos D. ;
Comas, David ;
Friedman, Eitan ;
Pe'er, Itsik ;
Ostrer, Harry .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (34) :13865-13870
[18]   Deep resequencing reveals excess rare recent variants consistent with explosive population growth [J].
Coventry, Alex ;
Bull-Otterson, Lara M. ;
Liu, Xiaoming ;
Clark, Andrew G. ;
Maxwell, Taylor J. ;
Crosby, Jacy ;
Hixson, James E. ;
Rea, Thomas J. ;
Muzny, Donna M. ;
Lewis, Lora R. ;
Wheeler, David A. ;
Sabo, Aniko ;
Lusk, Christine ;
Weiss, Kenneth G. ;
Akbar, Humeira ;
Cree, Andrew ;
Hawes, Alicia C. ;
Newsham, Irene ;
Varghese, Robin T. ;
Villasana, Donna ;
Gross, Shannon ;
Joshi, Vandita ;
Santibanez, Jireh ;
Morgan, Margaret ;
Chang, Kyle ;
Hale, Walker ;
Templeton, Alan R. ;
Boerwinkle, Eric ;
Gibbs, Richard ;
Sing, Charles F. .
NATURE COMMUNICATIONS, 2010, 1
[19]   The variant call format and VCFtools [J].
Danecek, Petr ;
Auton, Adam ;
Abecasis, Goncalo ;
Albers, Cornelis A. ;
Banks, Eric ;
DePristo, Mark A. ;
Handsaker, Robert E. ;
Lunter, Gerton ;
Marth, Gabor T. ;
Sherry, Stephen T. ;
McVean, Gilean ;
Durbin, Richard .
BIOINFORMATICS, 2011, 27 (15) :2156-2158
[20]   fastsimcoal: a continuous-time coalescent simulator of genomic diversity under arbitrarily complex evolutionary scenarios [J].
Excoffier, Laurent ;
Foll, Matthieu .
BIOINFORMATICS, 2011, 27 (09) :1332-1334