On individual genome-wide association studies and their meta-analysis

被引:19
|
作者
Pei, Yu-Fang [1 ,2 ]
Zhang, Lei [1 ,2 ]
Papasian, Christopher J. [3 ]
Wang, Yu-Ping [2 ]
Deng, Hong-Wen [1 ,2 ]
机构
[1] Univ Shanghai Sci & Technol, Ctr Syst Biomed Sci, Shanghai 200093, Peoples R China
[2] Tulane Univ, Ctr Bioinformat & Genom, Dept Biostat & Bioinformat, Sch Publ Hlth & Trop Med, New Orleans, LA 70112 USA
[3] Univ Missouri, Dept Basic Med Sci, Kansas City, MO 64108 USA
基金
中国国家自然科学基金;
关键词
BONE-MINERAL DENSITY; GENETIC ASSOCIATION; LOCI; HETEROGENEITY; REPLICATION; INCONSISTENCY; EFFICIENCY; VARIANTS; POWER;
D O I
10.1007/s00439-013-1366-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Individual genome-wide association (GWA) studies and their meta-analyses represent two approaches for identifying genetic loci associated with complex diseases/traits. Inconsistent findings and non-replicability between individual GWA studies and meta-analyses are commonly observed, hence posing the critical question as to how to interpret their respective results properly. In this study, we performed a series of simulation studies to investigate and compare the statistical properties of the two approaches. Our results show that (1) as expected, meta-analysis of larger sample size is more powerful than individual GWA studies under the ideal setting of population homogeneity among individual studies; (2) under the realistic setting of heterogeneity among individual studies, detection of heterogeneity is usually difficult and meta-analysis (even with the random-effects model) may introduce elevated false positive and/or negative rates; (3) despite relatively small sample size, well-designed individual GWA study has the capacity to identify novel loci for complex traits; (4) replicability between meta-analysis and independent individual studies or between independent meta-analyses is limited, and thus inconsistent findings are not unexpected.
引用
收藏
页码:265 / 279
页数:15
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