Genome-wide association analyses of expression phenotypes

被引:0
|
作者
Chen, Gary K. [1 ]
Zheng, Tian [2 ]
Witte, John S. [1 ]
Goode, Ellen L. [3 ]
机构
[1] Univ Calif San Francisco, Inst Human Genet, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[2] Columbia Univ, Dept Stat, New York, NY USA
[3] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN USA
关键词
Genetic Analysis Workshop; linkage; association; machine learning approaches; expression data; single nucleotide polymorphisms;
D O I
10.1002/gepi.20275
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of issues arise when analyzing the large amount of data from high-throughput genotype and expression microarray experiments, including design and interpretation of genome-wide association studies of expression phenotypes. These issues were considered by contributions submitted to Group 1 of the Genetic Analysis Workshop 15 (GAW15), which focused on the association of quantitative expression data. These contributions evaluated diverse hypotheses, including those relevant to cancer and obesity research, and used various analytic techniques, many of which were derived from information theory. Several observations from these reports stand out. First, one needs to consider the genetic model of the trait of interest and carefully select which single nucleotide polymorphisms and individuals are included early in the design stage of a study Second, by targeting specific pathways when analyzing genome-wide data, one can generate more interpretable results than agnostic approaches. Finally, for clatasets with small sample sizes but a large number of features like the Genetic Analysis Workshop 15 dataset, machine learning approaches may be more practical than traditional parametric approaches.
引用
收藏
页码:S7 / S11
页数:5
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