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Functional assessment of time course microarray data

MOTIVATION: Time-course microarray experiments study the progress of gene expression along time across one or several experimental conditions. Most developed analysis methods focus on the clustering or the differential expression analysis of genes and do not integrate functional information. The ass...

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Autores principales: Nueda, María José, Sebastián, Patricia, Tarazona, Sonia, García-García, Francisco, Dopazo, Joaquín, Ferrer, Alberto, Conesa, Ana
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697656/
https://www.ncbi.nlm.nih.gov/pubmed/19534758
http://dx.doi.org/10.1186/1471-2105-10-S6-S9
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author Nueda, María José
Sebastián, Patricia
Tarazona, Sonia
García-García, Francisco
Dopazo, Joaquín
Ferrer, Alberto
Conesa, Ana
author_facet Nueda, María José
Sebastián, Patricia
Tarazona, Sonia
García-García, Francisco
Dopazo, Joaquín
Ferrer, Alberto
Conesa, Ana
author_sort Nueda, María José
collection PubMed
description MOTIVATION: Time-course microarray experiments study the progress of gene expression along time across one or several experimental conditions. Most developed analysis methods focus on the clustering or the differential expression analysis of genes and do not integrate functional information. The assessment of the functional aspects of time-course transcriptomics data requires the use of approaches that exploit the activation dynamics of the functional categories to where genes are annotated. METHODS: We present three novel methodologies for the functional assessment of time-course microarray data. i) maSigFun derives from the maSigPro method, a regression-based strategy to model time-dependent expression patterns and identify genes with differences across series. maSigFun fits a regression model for groups of genes labeled by a functional class and selects those categories which have a significant model. ii) PCA-maSigFun fits a PCA model of each functional class-defined expression matrix to extract orthogonal patterns of expression change, which are then assessed for their fit to a time-dependent regression model. iii) ASCA-functional uses the ASCA model to rank genes according to their correlation to principal time expression patterns and assess functional enrichment on a GSA fashion. We used simulated and experimental datasets to study these novel approaches. Results were compared to alternative methodologies. RESULTS: Synthetic and experimental data showed that the different methods are able to capture different aspects of the relationship between genes, functions and co-expression that are biologically meaningful. The methods should not be considered as competitive but they provide different insights into the molecular and functional dynamic events taking place within the biological system under study.
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spelling pubmed-26976562009-06-16 Functional assessment of time course microarray data Nueda, María José Sebastián, Patricia Tarazona, Sonia García-García, Francisco Dopazo, Joaquín Ferrer, Alberto Conesa, Ana BMC Bioinformatics Proceedings MOTIVATION: Time-course microarray experiments study the progress of gene expression along time across one or several experimental conditions. Most developed analysis methods focus on the clustering or the differential expression analysis of genes and do not integrate functional information. The assessment of the functional aspects of time-course transcriptomics data requires the use of approaches that exploit the activation dynamics of the functional categories to where genes are annotated. METHODS: We present three novel methodologies for the functional assessment of time-course microarray data. i) maSigFun derives from the maSigPro method, a regression-based strategy to model time-dependent expression patterns and identify genes with differences across series. maSigFun fits a regression model for groups of genes labeled by a functional class and selects those categories which have a significant model. ii) PCA-maSigFun fits a PCA model of each functional class-defined expression matrix to extract orthogonal patterns of expression change, which are then assessed for their fit to a time-dependent regression model. iii) ASCA-functional uses the ASCA model to rank genes according to their correlation to principal time expression patterns and assess functional enrichment on a GSA fashion. We used simulated and experimental datasets to study these novel approaches. Results were compared to alternative methodologies. RESULTS: Synthetic and experimental data showed that the different methods are able to capture different aspects of the relationship between genes, functions and co-expression that are biologically meaningful. The methods should not be considered as competitive but they provide different insights into the molecular and functional dynamic events taking place within the biological system under study. BioMed Central 2009-06-16 /pmc/articles/PMC2697656/ /pubmed/19534758 http://dx.doi.org/10.1186/1471-2105-10-S6-S9 Text en Copyright © 2009 Nueda 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 Proceedings
Nueda, María José
Sebastián, Patricia
Tarazona, Sonia
García-García, Francisco
Dopazo, Joaquín
Ferrer, Alberto
Conesa, Ana
Functional assessment of time course microarray data
title Functional assessment of time course microarray data
title_full Functional assessment of time course microarray data
title_fullStr Functional assessment of time course microarray data
title_full_unstemmed Functional assessment of time course microarray data
title_short Functional assessment of time course microarray data
title_sort functional assessment of time course microarray data
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697656/
https://www.ncbi.nlm.nih.gov/pubmed/19534758
http://dx.doi.org/10.1186/1471-2105-10-S6-S9
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