Refining gene signatures: a Bayesian approach

<p>Abstract</p> <p>Background</p> <p>In high density arrays, the identification of relevant genes for disease classification is complicated by not only the curse of dimensionality but also the highly correlated nature of the array data. In this paper, we are interested...

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Main Authors: Labbe Aurélie, Djebbari Amira
Format: Article
Language:English
Published: BMC 2009-12-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/10/410
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spelling doaj-4f8e501d6cf548e889128ff909a36f722020-11-25T01:26:47ZengBMCBMC Bioinformatics1471-21052009-12-0110141010.1186/1471-2105-10-410Refining gene signatures: a Bayesian approachLabbe AurélieDjebbari Amira<p>Abstract</p> <p>Background</p> <p>In high density arrays, the identification of relevant genes for disease classification is complicated by not only the curse of dimensionality but also the highly correlated nature of the array data. In this paper, we are interested in the question of how many and which genes should be selected for a disease class prediction. Our work consists of a Bayesian supervised statistical learning approach to refine gene signatures with a regularization which penalizes for the correlation between the variables selected.</p> <p>Results</p> <p>Our simulation results show that we can most often recover the correct subset of genes that predict the class as compared to other methods, even when accuracy and subset size remain the same. On real microarray datasets, we show that our approach can refine gene signatures to obtain either the same or better predictive performance than other existing methods with a smaller number of genes.</p> <p>Conclusions</p> <p>Our novel Bayesian approach includes a prior which penalizes highly correlated features in model selection and is able to extract key genes in the highly correlated context of microarray data. The methodology in the paper is described in the context of microarray data, but can be applied to any array data (such as micro RNA, for example) as a first step towards predictive modeling of cancer pathways. A user-friendly software implementation of the method is available.</p> http://www.biomedcentral.com/1471-2105/10/410
collection DOAJ
language English
format Article
sources DOAJ
author Labbe Aurélie
Djebbari Amira
spellingShingle Labbe Aurélie
Djebbari Amira
Refining gene signatures: a Bayesian approach
BMC Bioinformatics
author_facet Labbe Aurélie
Djebbari Amira
author_sort Labbe Aurélie
title Refining gene signatures: a Bayesian approach
title_short Refining gene signatures: a Bayesian approach
title_full Refining gene signatures: a Bayesian approach
title_fullStr Refining gene signatures: a Bayesian approach
title_full_unstemmed Refining gene signatures: a Bayesian approach
title_sort refining gene signatures: a bayesian approach
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2009-12-01
description <p>Abstract</p> <p>Background</p> <p>In high density arrays, the identification of relevant genes for disease classification is complicated by not only the curse of dimensionality but also the highly correlated nature of the array data. In this paper, we are interested in the question of how many and which genes should be selected for a disease class prediction. Our work consists of a Bayesian supervised statistical learning approach to refine gene signatures with a regularization which penalizes for the correlation between the variables selected.</p> <p>Results</p> <p>Our simulation results show that we can most often recover the correct subset of genes that predict the class as compared to other methods, even when accuracy and subset size remain the same. On real microarray datasets, we show that our approach can refine gene signatures to obtain either the same or better predictive performance than other existing methods with a smaller number of genes.</p> <p>Conclusions</p> <p>Our novel Bayesian approach includes a prior which penalizes highly correlated features in model selection and is able to extract key genes in the highly correlated context of microarray data. The methodology in the paper is described in the context of microarray data, but can be applied to any array data (such as micro RNA, for example) as a first step towards predictive modeling of cancer pathways. A user-friendly software implementation of the method is available.</p>
url http://www.biomedcentral.com/1471-2105/10/410
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