Skip Navigation


Bioinformatics Advance Access originally published online on December 7, 2004
Bioinformatics 2005 21(8):1530-1537; doi:10.1093/bioinformatics/bti192
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow All Versions of this Article:
21/8/1530    most recent
bti192v1
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 (12)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Wang, Y.
Right arrow Articles by Pearlman, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, Y.
Right arrow Articles by Pearlman, J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2004. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions{at}oupjournals.org

HykGene: a hybrid approach for selecting marker genes for phenotype classification using microarray gene expression data

Yuhang Wang 1,*, Fillia S. Makedon 1, James C. Ford 2 and Justin Pearlman 2,3

1Department of Computer Science, Dartmouth College 6211 Sudikoff Laboratory, Hanover, NH 03755-3510, USA
2Department of Medicine, Dartmouth-Hitchcock Medical Center, Dartmouth Medical School 1 Rope Ferry Road, Hanover, NH 03755-1404, USA
3Department of Radiology, Dartmouth-Hitchcock Medical Center One Medical Center Drive, Lebanon, NH 03756, USA

*To whom correspondence should be addressed.

Motivation: Recent studies have shown that microarray gene expression data are useful for phenotype classification of many diseases. A major problem in this classification is that the number of features (genes) greatly exceeds the number of instances (tissue samples). It has been shown that selecting a small set of informative genes can lead to improved classification accuracy. Many approaches have been proposed for this gene selection problem. Most of the previous gene ranking methods typically select 50–200 top-ranked genes and these genes are often highly correlated. Our goal is to select a small set of non-redundant marker genes that are most relevant for the classification task.

Results: To achieve this goal, we developed a novel hybrid approach that combines gene ranking and clustering analysis. In this approach, we first applied feature filtering algorithms to select a set of top-ranked genes, and then applied hierarchical clustering on these genes to generate a dendrogram. Finally, the dendrogram was analyzed by a sweep-line algorithm and marker genes are selected by collapsing dense clusters. Empirical study using three public datasets shows that our approach is capable of selecting relatively few marker genes while offering the same or better leave-one-out cross-validation accuracy compared with approaches that use top-ranked genes directly for classification.

Availability: The HykGene software is freely available at http://www.cs.dartmouth.edu/~wyh/software.htm

Contact: wyh{at}cs.dartmouth.edu

Supplementary information: Supplementary material is available from http://www.cs.dartmouth.edu/~wyh/hykgene/supplement/index.htm


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
CirculationHome page
T. W. Chittenden, J. A. Sherman, F. Xiong, A. E. Hall, A. A. Lanahan, J. M. Taylor, H. Duan, J. D. Pearlman, J. H. Moore, S. M. Schwartz, et al.
Transcriptional Profiling in Coronary Artery Disease: Indications for Novel Markers of Coronary Collateralization
Circulation, October 24, 2006; 114(17): 1811 - 1820.
[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.