Skip Navigation


Bioinformatics Advance Access originally published online on August 27, 2008
Bioinformatics 2008 24(21):2474-2481; doi:10.1093/bioinformatics/btn458
This Article
Right arrow Full Text
Right arrow Full Text (Print PDF)
Right arrow All Versions of this Article:
24/21/2474    most recent
btn458v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (2)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Chen, X.
Right arrow Articles by Zhang, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chen, X.
Right arrow Articles by Zhang, B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Supervised principal component analysis for gene set enrichment of microarray data with continuous or survival outcomes

Xi Chen 1,*,{dagger}, Lily Wang 2,{dagger}, Jonathan D. Smith 3 and Bing Zhang 4

1Department of Quantitative Health Sciences, The Cleveland Clinic, 9500 Euclid Ave. Cleveland, OH 44195, 2Department of Biostatistics, Vanderbilt University, Nashville, TN 37232, 3Department of Cell Biology, The Cleveland Clinic, 9500 Euclid Ave. Cleveland, OH 44195 and 4Department of Biomedical Informatics, Vanderbilt University, Nashville, TN 37232, USA

*To whom correspondence should be addressed.


   Abstract

Motivation: Gene set analysis allows formal testing of subtle but coordinated changes in a group of genes, such as those defined by Gene Ontology (GO) or KEGG Pathway databases. We propose a new method for gene set analysis that is based on principal component analysis (PCA) of genes expression values in the gene set. PCA is an effective method for reducing high dimensionality and capture variations in gene expression values. However, one limitation with PCA is that the latent variable identified by the first PC may be unrelated to outcome.

Results: In the proposed supervised PCA (SPCA) model for gene set analysis, the PCs are estimated from a selected subset of genes that are associated with outcome. As outcome information is used in the gene selection step, this method is supervised, thus called the Supervised PCA model. Because of the gene selection step, test statistic in SPCA model can no longer be approximated well using t-distribution. We propose a two-component mixture distribution based on Gumbel exteme value distributions to account for the gene selection step. We show the proposed method compares favorably to currently available gene set analysis methods using simulated and real microarray data.

Software: The R code for the analysis used in this article are available upon request, we are currently working on implementing the proposed method in an R package.

Contact: chenx3{at}ccf.org.

{dagger}The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.

Associate Editor: David Rocke


Received on February 4, 2008; revised on August 19, 2008; accepted on August 22, 2008

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
BioinformaticsHome page
S. Ma and M. R. Kosorok
Identification of differential gene pathways with principal component analysis
Bioinformatics, April 1, 2009; 25(7): 882 - 889.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.