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Genome‐wide association analyses of expression phenotypes
Author(s) -
Chen Gary K.,
Zheng Tian,
Witte John S.,
Goode Ellen L.
Publication year - 2007
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.20275
Subject(s) - computational biology , genetic association , genome wide association study , trait , biology , genome , single nucleotide polymorphism , computer science , genetics , genotype , gene , programming language
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 datasets 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. Genet Epidemiol 31 (Suppl. 1): S7–S11, 2007. © 2007 Wiley‐Liss, Inc.