Biclustering of gene expression data by non-smooth non-negative matrix factorization

<p>Abstract</p> <p>Background</p> <p>The extended use of microarray technologies has enabled the generation and accumulation of gene expression datasets that contain expression levels of thousands of genes across tens or hundreds of different experimental conditions. On...

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Main Authors: Carazo Jose M, Tirado F, Pascual-Marqui Roberto D, Carmona-Saez Pedro, Pascual-Montano Alberto
Format: Article
Language:English
Published: BMC 2006-02-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/7/78
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spelling doaj-8297f131ab88499ba73bee3f4d5ebc912020-11-25T01:39:12ZengBMCBMC Bioinformatics1471-21052006-02-01717810.1186/1471-2105-7-78Biclustering of gene expression data by non-smooth non-negative matrix factorizationCarazo Jose MTirado FPascual-Marqui Roberto DCarmona-Saez PedroPascual-Montano Alberto<p>Abstract</p> <p>Background</p> <p>The extended use of microarray technologies has enabled the generation and accumulation of gene expression datasets that contain expression levels of thousands of genes across tens or hundreds of different experimental conditions. One of the major challenges in the analysis of such datasets is to discover local structures composed by sets of genes that show coherent expression patterns across subsets of experimental conditions. These patterns may provide clues about the main biological processes associated to different physiological states.</p> <p>Results</p> <p>In this work we present a methodology able to cluster genes and conditions highly related in sub-portions of the data. Our approach is based on a new data mining technique, Non-smooth Non-Negative Matrix Factorization (<it>n</it>sNMF), able to identify localized patterns in large datasets. We assessed the potential of this methodology analyzing several synthetic datasets as well as two large and heterogeneous sets of gene expression profiles. In all cases the method was able to identify localized features related to sets of genes that show consistent expression patterns across subsets of experimental conditions. The uncovered structures showed a clear biological meaning in terms of relationships among functional annotations of genes and the phenotypes or physiological states of the associated conditions.</p> <p>Conclusion</p> <p>The proposed approach can be a useful tool to analyze large and heterogeneous gene expression datasets. The method is able to identify complex relationships among genes and conditions that are difficult to identify by standard clustering algorithms.</p> http://www.biomedcentral.com/1471-2105/7/78
collection DOAJ
language English
format Article
sources DOAJ
author Carazo Jose M
Tirado F
Pascual-Marqui Roberto D
Carmona-Saez Pedro
Pascual-Montano Alberto
spellingShingle Carazo Jose M
Tirado F
Pascual-Marqui Roberto D
Carmona-Saez Pedro
Pascual-Montano Alberto
Biclustering of gene expression data by non-smooth non-negative matrix factorization
BMC Bioinformatics
author_facet Carazo Jose M
Tirado F
Pascual-Marqui Roberto D
Carmona-Saez Pedro
Pascual-Montano Alberto
author_sort Carazo Jose M
title Biclustering of gene expression data by non-smooth non-negative matrix factorization
title_short Biclustering of gene expression data by non-smooth non-negative matrix factorization
title_full Biclustering of gene expression data by non-smooth non-negative matrix factorization
title_fullStr Biclustering of gene expression data by non-smooth non-negative matrix factorization
title_full_unstemmed Biclustering of gene expression data by non-smooth non-negative matrix factorization
title_sort biclustering of gene expression data by non-smooth non-negative matrix factorization
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2006-02-01
description <p>Abstract</p> <p>Background</p> <p>The extended use of microarray technologies has enabled the generation and accumulation of gene expression datasets that contain expression levels of thousands of genes across tens or hundreds of different experimental conditions. One of the major challenges in the analysis of such datasets is to discover local structures composed by sets of genes that show coherent expression patterns across subsets of experimental conditions. These patterns may provide clues about the main biological processes associated to different physiological states.</p> <p>Results</p> <p>In this work we present a methodology able to cluster genes and conditions highly related in sub-portions of the data. Our approach is based on a new data mining technique, Non-smooth Non-Negative Matrix Factorization (<it>n</it>sNMF), able to identify localized patterns in large datasets. We assessed the potential of this methodology analyzing several synthetic datasets as well as two large and heterogeneous sets of gene expression profiles. In all cases the method was able to identify localized features related to sets of genes that show consistent expression patterns across subsets of experimental conditions. The uncovered structures showed a clear biological meaning in terms of relationships among functional annotations of genes and the phenotypes or physiological states of the associated conditions.</p> <p>Conclusion</p> <p>The proposed approach can be a useful tool to analyze large and heterogeneous gene expression datasets. The method is able to identify complex relationships among genes and conditions that are difficult to identify by standard clustering algorithms.</p>
url http://www.biomedcentral.com/1471-2105/7/78
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