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M-BISON: Microarray-based integration of data sources using networks

BACKGROUND: The accurate detection of differentially expressed (DE) genes has become a central task in microarray analysis. Unfortunately, the noise level and experimental variability of microarrays can be limiting. While a number of existing methods partially overcome these limitations by incorpora...

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Detalles Bibliográficos
Autores principales: Daigle, Bernie J, Altman, Russ B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396182/
https://www.ncbi.nlm.nih.gov/pubmed/18439292
http://dx.doi.org/10.1186/1471-2105-9-214
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author Daigle, Bernie J
Altman, Russ B
author_facet Daigle, Bernie J
Altman, Russ B
author_sort Daigle, Bernie J
collection PubMed
description BACKGROUND: The accurate detection of differentially expressed (DE) genes has become a central task in microarray analysis. Unfortunately, the noise level and experimental variability of microarrays can be limiting. While a number of existing methods partially overcome these limitations by incorporating biological knowledge in the form of gene groups, these methods sacrifice gene-level resolution. This loss of precision can be inappropriate, especially if the desired output is a ranked list of individual genes. To address this shortcoming, we developed M-BISON (Microarray-Based Integration of data SOurces using Networks), a formal probabilistic model that integrates background biological knowledge with microarray data to predict individual DE genes. RESULTS: M-BISON improves signal detection on a range of simulated data, particularly when using very noisy microarray data. We also applied the method to the task of predicting heat shock-related differentially expressed genes in S. cerevisiae, using an hsf1 mutant microarray dataset and conserved yeast DNA sequence motifs. Our results demonstrate that M-BISON improves the analysis quality and makes predictions that are easy to interpret in concert with incorporated knowledge. Specifically, M-BISON increases the AUC of DE gene prediction from .541 to .623 when compared to a method using only microarray data, and M-BISON outperforms a related method, GeneRank. Furthermore, by analyzing M-BISON predictions in the context of the background knowledge, we identified YHR124W as a potentially novel player in the yeast heat shock response. CONCLUSION: This work provides a solid foundation for the principled integration of imperfect biological knowledge with gene expression data and other high-throughput data sources.
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spelling pubmed-23961822008-05-28 M-BISON: Microarray-based integration of data sources using networks Daigle, Bernie J Altman, Russ B BMC Bioinformatics Research Article BACKGROUND: The accurate detection of differentially expressed (DE) genes has become a central task in microarray analysis. Unfortunately, the noise level and experimental variability of microarrays can be limiting. While a number of existing methods partially overcome these limitations by incorporating biological knowledge in the form of gene groups, these methods sacrifice gene-level resolution. This loss of precision can be inappropriate, especially if the desired output is a ranked list of individual genes. To address this shortcoming, we developed M-BISON (Microarray-Based Integration of data SOurces using Networks), a formal probabilistic model that integrates background biological knowledge with microarray data to predict individual DE genes. RESULTS: M-BISON improves signal detection on a range of simulated data, particularly when using very noisy microarray data. We also applied the method to the task of predicting heat shock-related differentially expressed genes in S. cerevisiae, using an hsf1 mutant microarray dataset and conserved yeast DNA sequence motifs. Our results demonstrate that M-BISON improves the analysis quality and makes predictions that are easy to interpret in concert with incorporated knowledge. Specifically, M-BISON increases the AUC of DE gene prediction from .541 to .623 when compared to a method using only microarray data, and M-BISON outperforms a related method, GeneRank. Furthermore, by analyzing M-BISON predictions in the context of the background knowledge, we identified YHR124W as a potentially novel player in the yeast heat shock response. CONCLUSION: This work provides a solid foundation for the principled integration of imperfect biological knowledge with gene expression data and other high-throughput data sources. BioMed Central 2008-04-25 /pmc/articles/PMC2396182/ /pubmed/18439292 http://dx.doi.org/10.1186/1471-2105-9-214 Text en Copyright © 2008 Daigle and Altman; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Daigle, Bernie J
Altman, Russ B
M-BISON: Microarray-based integration of data sources using networks
title M-BISON: Microarray-based integration of data sources using networks
title_full M-BISON: Microarray-based integration of data sources using networks
title_fullStr M-BISON: Microarray-based integration of data sources using networks
title_full_unstemmed M-BISON: Microarray-based integration of data sources using networks
title_short M-BISON: Microarray-based integration of data sources using networks
title_sort m-bison: microarray-based integration of data sources using networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396182/
https://www.ncbi.nlm.nih.gov/pubmed/18439292
http://dx.doi.org/10.1186/1471-2105-9-214
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