A dynamic model for genome-wide association studies

被引:75
作者
Das, Kiranmoy [1 ]
Li, Jiahan [1 ]
Wang, Zhong [2 ]
Tong, Chunfa [2 ]
Fu, Guifang [1 ]
Li, Yao [3 ]
Xu, Meng [2 ]
Ahn, Kwangmi [2 ]
Mauger, David [2 ]
Li, Runze [1 ,2 ]
Wu, Rongling [1 ,2 ]
机构
[1] Penn State Univ, Dept Stat, University Pk, PA 16802 USA
[2] Penn State Coll Med, Dept Publ Hlth Sci, Hershey, PA USA
[3] W Virginia Univ, Dept Stat, Morgantown, WV 26506 USA
关键词
BODY-MASS INDEX; MISSING HERITABILITY; IDENTIFIES; 5; FTO GENE; GROWTH; VARIANTS; INSIGHTS; TRAITS; LOCI;
D O I
10.1007/s00439-011-0960-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although genome-wide association studies (GWAS) are widely used to identify the genetic and environmental etiology of a trait, several key issues related to their statistical power and biological relevance have remained unexplored. Here, we describe a novel statistical approach, called functional GWAS or fGWAS, to analyze the genetic control of traits by integrating biological principles of trait formation into the GWAS framework through mathematical and statistical bridges. fGWAS can address many fundamental questions, such as the patterns of genetic control over development, the duration of genetic effects, as well as what causes developmental trajectories to change or stop changing. In statistics, fGWAS displays increased power for gene detection by capitalizing on cumulative phenotypic variation in a longitudinal trait over time and increased robustness for manipulating sparse longitudinal data.
引用
收藏
页码:629 / 639
页数:11
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