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Sparse canonical methods for biological data integration: application to a cross-platform study

BACKGROUND: In the context of systems biology, few sparse approaches have been proposed so far to integrate several data sets. It is however an important and fundamental issue that will be widely encountered in post genomic studies, when simultaneously analyzing transcriptomics, proteomics and metab...

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Autores principales: Lê Cao, Kim-Anh, Martin, Pascal GP, Robert-Granié, Christèle, Besse, Philippe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640358/
https://www.ncbi.nlm.nih.gov/pubmed/19171069
http://dx.doi.org/10.1186/1471-2105-10-34
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author Lê Cao, Kim-Anh
Martin, Pascal GP
Robert-Granié, Christèle
Besse, Philippe
author_facet Lê Cao, Kim-Anh
Martin, Pascal GP
Robert-Granié, Christèle
Besse, Philippe
author_sort Lê Cao, Kim-Anh
collection PubMed
description BACKGROUND: In the context of systems biology, few sparse approaches have been proposed so far to integrate several data sets. It is however an important and fundamental issue that will be widely encountered in post genomic studies, when simultaneously analyzing transcriptomics, proteomics and metabolomics data using different platforms, so as to understand the mutual interactions between the different data sets. In this high dimensional setting, variable selection is crucial to give interpretable results. We focus on a sparse Partial Least Squares approach (sPLS) to handle two-block data sets, where the relationship between the two types of variables is known to be symmetric. Sparse PLS has been developed either for a regression or a canonical correlation framework and includes a built-in procedure to select variables while integrating data. To illustrate the canonical mode approach, we analyzed the NCI60 data sets, where two different platforms (cDNA and Affymetrix chips) were used to study the transcriptome of sixty cancer cell lines. RESULTS: We compare the results obtained with two other sparse or related canonical correlation approaches: CCA with Elastic Net penalization (CCA-EN) and Co-Inertia Analysis (CIA). The latter does not include a built-in procedure for variable selection and requires a two-step analysis. We stress the lack of statistical criteria to evaluate canonical correlation methods, which makes biological interpretation absolutely necessary to compare the different gene selections. We also propose comprehensive graphical representations of both samples and variables to facilitate the interpretation of the results. CONCLUSION: sPLS and CCA-EN selected highly relevant genes and complementary findings from the two data sets, which enabled a detailed understanding of the molecular characteristics of several groups of cell lines. These two approaches were found to bring similar results, although they highlighted the same phenomenons with a different priority. They outperformed CIA that tended to select redundant information.
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spelling pubmed-26403582009-02-12 Sparse canonical methods for biological data integration: application to a cross-platform study Lê Cao, Kim-Anh Martin, Pascal GP Robert-Granié, Christèle Besse, Philippe BMC Bioinformatics Research Article BACKGROUND: In the context of systems biology, few sparse approaches have been proposed so far to integrate several data sets. It is however an important and fundamental issue that will be widely encountered in post genomic studies, when simultaneously analyzing transcriptomics, proteomics and metabolomics data using different platforms, so as to understand the mutual interactions between the different data sets. In this high dimensional setting, variable selection is crucial to give interpretable results. We focus on a sparse Partial Least Squares approach (sPLS) to handle two-block data sets, where the relationship between the two types of variables is known to be symmetric. Sparse PLS has been developed either for a regression or a canonical correlation framework and includes a built-in procedure to select variables while integrating data. To illustrate the canonical mode approach, we analyzed the NCI60 data sets, where two different platforms (cDNA and Affymetrix chips) were used to study the transcriptome of sixty cancer cell lines. RESULTS: We compare the results obtained with two other sparse or related canonical correlation approaches: CCA with Elastic Net penalization (CCA-EN) and Co-Inertia Analysis (CIA). The latter does not include a built-in procedure for variable selection and requires a two-step analysis. We stress the lack of statistical criteria to evaluate canonical correlation methods, which makes biological interpretation absolutely necessary to compare the different gene selections. We also propose comprehensive graphical representations of both samples and variables to facilitate the interpretation of the results. CONCLUSION: sPLS and CCA-EN selected highly relevant genes and complementary findings from the two data sets, which enabled a detailed understanding of the molecular characteristics of several groups of cell lines. These two approaches were found to bring similar results, although they highlighted the same phenomenons with a different priority. They outperformed CIA that tended to select redundant information. BioMed Central 2009-01-26 /pmc/articles/PMC2640358/ /pubmed/19171069 http://dx.doi.org/10.1186/1471-2105-10-34 Text en Copyright © 2009 Lê Cao et al; 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
Lê Cao, Kim-Anh
Martin, Pascal GP
Robert-Granié, Christèle
Besse, Philippe
Sparse canonical methods for biological data integration: application to a cross-platform study
title Sparse canonical methods for biological data integration: application to a cross-platform study
title_full Sparse canonical methods for biological data integration: application to a cross-platform study
title_fullStr Sparse canonical methods for biological data integration: application to a cross-platform study
title_full_unstemmed Sparse canonical methods for biological data integration: application to a cross-platform study
title_short Sparse canonical methods for biological data integration: application to a cross-platform study
title_sort sparse canonical methods for biological data integration: application to a cross-platform study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640358/
https://www.ncbi.nlm.nih.gov/pubmed/19171069
http://dx.doi.org/10.1186/1471-2105-10-34
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