Pooled Association Tests for Rare Genetic Variants: A Review and Some New Results

被引:55
|
作者
Derkach, Andriy [1 ]
Lawless, Jerry F. [2 ,3 ]
Sun, Lei [1 ,3 ]
机构
[1] Univ Toronto, Dept Stat Sci, Toronto, ON 1M5S 3G3, Canada
[2] Univ Waterloo, Dept Stat & Actuarial Sci, Waterloo, ON N2L 3G1, Canada
[3] Univ Toronto, Dalla Lana Sch Publ Hlth, Div Biostat, Toronto, ON M5T 3M7, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
Linear statistics; quadratic statistics; score tests; weighting; power; next generation sequencing; complex traits; LINKAGE DISEQUILIBRIUM; SEQUENCING ASSOCIATION; DISEASE ASSOCIATION; STATISTICAL TESTS; COMMON DISEASES; HUMAN GENOME; TRAITS; LOCI;
D O I
10.1214/13-STS456
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
In the search for genetic factors that are associated with complex heritable human traits, considerable attention is now being focused on rare variants that individually have small effects. In response, numerous recent papers have proposed testing strategies to assess association between a group of rare variants and a trait, with competing claims about the performance of various tests. The power of a given test in fact depends on the nature of any association and on the rareness of the variants in question. We review such tests within a general framework that covers a wide range of genetic models and types of data. We study the performance of specific tests through exact or asymptotic power formulas and through novel simulation studies of over 10,000 different models. The tests considered are also applied to real sequence data from the 1000 Genomes project and provided by the GAW17. We recommend a testing strategy, but our results show that power to detect association in plausible genetic scenarios is low for studies of medium size unless a high proportion of the chosen variants are causal. Consequently, considerable attention must be given to relevant biological information that can guide the selection of variants for testing.
引用
收藏
页码:302 / 321
页数:20
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