Skip Navigation



Bioinformatics Advance Access published online on July 15, 2004

Bioinformatics, doi:10.1093/bioinformatics/bth419
Bioinformatics © Oxford University Press 2004; all rights reserved
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
20/18/3423    most recent
bth419v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
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 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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Bae, K.
Right arrow Articles by Mallick, B. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bae, K.
Right arrow Articles by Mallick, B. K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received March 3, 2004
Revised July 9, 2004
Accepted July 10, 2004

Article

Gene selection using a two-level hierarchical Bayesian model

Kyounghwa Bae 1 Bani K. Mallick 1*

1 Department of Statistics, Texas A&M University, College Station, TX, 77843-3143, USA

* To whom correspondence should be addressed. E-mail: bmallick{at}stat.tamu.edu.


   Abstract

The fundamental problem of gene selection via cDNA data is to identify which genes are differentially expressed across different kinds of tissue samples (e.g. normal and cancer). cDNA data contains large number of variables (genes) and usually the sample size is relatively small so the selection process can be unstable. Therefore, models which incorporate sparsity in terms of variables (genes) are desirable for this kind of problem. This paper proposes a two-level hierarchical Bayesian model for variable selection which assumes a prior that favors sparseness. We adopt a Markov Chain Monte Carlo (MCMC) based computation technique to simulate the parameters from the posteriors. The method is applied to leukemia data from Golub et al. (1999) and a published data set of Hendenfalk et al. (2001) on breast cancer.

Supplimentary website: http://stat.tamu.edu/people/faculty/bmallick.html.


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
GeneticsHome page
N. Yi and S. Banerjee
Hierarchical Generalized Linear Models for Multiple Quantitative Trait Locus Mapping
Genetics, March 1, 2009; 181(3): 1101 - 1113.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
N. Yi and S. Xu
Bayesian LASSO for Quantitative Trait Loci Mapping
Genetics, June 1, 2008; 179(2): 1045 - 1055.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
P. Sykacek, R. Clarkson, C. Print, R. Furlong, and G. Micklem
Bayesian modelling of shared gene function
Bioinformatics, August 1, 2007; 23(15): 1936 - 1944.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
H. H. Zhang, J. Ahn, X. Lin, and C. Park
Gene selection using support vector machines with non-convex penalty
Bioinformatics, January 1, 2006; 22(1): 88 - 95.
[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.