Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification

<p>Abstract</p> <p>Background</p> <p>Large-scale compilation of gene expression microarray datasets across diverse biological phenotypes provided a means of gathering a priori knowledge in the form of identification and annotation of bimodal genes in the human and mouse...

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Main Authors: Tozeren Aydin, Gormley Michael
Format: Article
Language:English
Published: BMC 2008-11-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/9/486
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spelling doaj-dcc9bbe69afc42258c78a4b2241d79e02020-11-25T00:13:40ZengBMCBMC Bioinformatics1471-21052008-11-019148610.1186/1471-2105-9-486Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classificationTozeren AydinGormley Michael<p>Abstract</p> <p>Background</p> <p>Large-scale compilation of gene expression microarray datasets across diverse biological phenotypes provided a means of gathering a priori knowledge in the form of identification and annotation of bimodal genes in the human and mouse genomes. These switch-like genes consist of 15% of known human genes, and are enriched with genes coding for extracellular and membrane proteins. It is of interest to determine the prediction potential of bimodal genes for class discovery in large-scale datasets.</p> <p>Results</p> <p>Use of a model-based clustering algorithm accurately classified more than 400 microarray samples into 19 different tissue types on the basis of bimodal gene expression. Bimodal expression patterns were also highly effective in differentiating between infectious diseases in model-based clustering of microarray data. Supervised classification with feature selection restricted to switch-like genes also recognized tissue specific and infectious disease specific signatures in independent test datasets reserved for validation. Determination of "on" and "off" states of switch-like genes in various tissues and diseases allowed for the identification of activated/deactivated pathways. Activated switch-like genes in neural, skeletal muscle and cardiac muscle tissue tend to have tissue-specific roles. A majority of activated genes in infectious disease are involved in processes related to the immune response.</p> <p>Conclusion</p> <p>Switch-like bimodal gene sets capture genome-wide signatures from microarray data in health and infectious disease. A subset of bimodal genes coding for extracellular and membrane proteins are associated with tissue specificity, indicating a potential role for them as biomarkers provided that expression is altered in the onset of disease. Furthermore, we provide evidence that bimodal genes are involved in temporally and spatially active mechanisms including tissue-specific functions and response of the immune system to invading pathogens.</p> http://www.biomedcentral.com/1471-2105/9/486
collection DOAJ
language English
format Article
sources DOAJ
author Tozeren Aydin
Gormley Michael
spellingShingle Tozeren Aydin
Gormley Michael
Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
BMC Bioinformatics
author_facet Tozeren Aydin
Gormley Michael
author_sort Tozeren Aydin
title Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
title_short Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
title_full Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
title_fullStr Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
title_full_unstemmed Expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
title_sort expression profiles of switch-like genes accurately classify tissue and infectious disease phenotypes in model-based classification
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2008-11-01
description <p>Abstract</p> <p>Background</p> <p>Large-scale compilation of gene expression microarray datasets across diverse biological phenotypes provided a means of gathering a priori knowledge in the form of identification and annotation of bimodal genes in the human and mouse genomes. These switch-like genes consist of 15% of known human genes, and are enriched with genes coding for extracellular and membrane proteins. It is of interest to determine the prediction potential of bimodal genes for class discovery in large-scale datasets.</p> <p>Results</p> <p>Use of a model-based clustering algorithm accurately classified more than 400 microarray samples into 19 different tissue types on the basis of bimodal gene expression. Bimodal expression patterns were also highly effective in differentiating between infectious diseases in model-based clustering of microarray data. Supervised classification with feature selection restricted to switch-like genes also recognized tissue specific and infectious disease specific signatures in independent test datasets reserved for validation. Determination of "on" and "off" states of switch-like genes in various tissues and diseases allowed for the identification of activated/deactivated pathways. Activated switch-like genes in neural, skeletal muscle and cardiac muscle tissue tend to have tissue-specific roles. A majority of activated genes in infectious disease are involved in processes related to the immune response.</p> <p>Conclusion</p> <p>Switch-like bimodal gene sets capture genome-wide signatures from microarray data in health and infectious disease. A subset of bimodal genes coding for extracellular and membrane proteins are associated with tissue specificity, indicating a potential role for them as biomarkers provided that expression is altered in the onset of disease. Furthermore, we provide evidence that bimodal genes are involved in temporally and spatially active mechanisms including tissue-specific functions and response of the immune system to invading pathogens.</p>
url http://www.biomedcentral.com/1471-2105/9/486
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AT gormleymichael expressionprofilesofswitchlikegenesaccuratelyclassifytissueandinfectiousdiseasephenotypesinmodelbasedclassification
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