Original Article
Genome-wide association analyses of expression phenotypes
Article first published online: 28 NOV 2007
DOI: 10.1002/gepi.20275
© 2007 Wiley-Liss, Inc.
Issue

Genetic Epidemiology
Supplement: Genetic Analysis Workshop 15: Summaries of the Design and Analysis of Genomic Data
Volume 31, Issue S1, pages S7–S11, 2007
Additional Information
How to Cite
Chen, G. K., Zheng, T., Witte, J. S. and Goode, E. L. (2007), Genome-wide association analyses of expression phenotypes. Genet. Epidemiol., 31: S7–S11. doi: 10.1002/gepi.20275
Publication History
- Issue published online: 28 NOV 2007
- Article first published online: 28 NOV 2007
- Abstract
- References
- Cited By
Keywords:
- Genetic Analysis Workshop;
- linkage;
- association;
- machine learning approaches;
- expression data;
- single nucleotide polymorphisms
Abstract
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.

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