共 26 条
A Fast, Powerful Method for Detecting Identity by Descent
被引:263
作者:

Browning, Brian L.
论文数: 0 引用数: 0
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机构:
Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98105 USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98105 USA

Browning, Sharon R.
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机构:
Univ Washington, Dept Biostat, Seattle, WA 98105 USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98105 USA
机构:
[1] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98105 USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98105 USA
基金:
英国惠康基金;
美国国家卫生研究院;
关键词:
WHOLE-GENOME ASSOCIATION;
HAPLOTYPE;
RELATEDNESS;
GENES;
MODEL;
D O I:
10.1016/j.ajhg.2011.01.010
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
We present a method, fastIBID, for finding tracts of identity by descent (IBD) between pairs of individuals. FastIBD can be applied to thousands of samples across genome-wide SNP data and is significantly more powerful for finding short tracts of IBD than existing methods for finding IBD tracts in such data. We show that fastIBD can detect facets of population structure that are not revealed by other methods. In the Wellcome Trust Case Control Consortium bipolar disorder case-control data, we find a genome-wide excess of IBD in case-case pairs of individuals compared to control-control pairs. We show that this excess can be explained by the geographical clustering of cases. We also show that it is possible to use fast! BD to generate highly accurate estimates of genome-wide IBD sharing between pairs of distant relatives. This is useful for estimation of relationship and for adjusting for relatedness in association studies. FastIBD is incorporated in the freely available Beagle software package.
引用
收藏
页码:173 / 182
页数:10
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