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A feature selection strategy for gene expression time series experiments with hidden Markov models

Studies conducted in time series could be far more informative than those that only capture a specific moment in time. However, when it comes to transcriptomic data, time points are sparse creating the need for a constant search for methods capable of extracting information out of experiments of thi...

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Autores principales: Cárdenas-Ovando, Roberto A., Fernández-Figueroa, Edith A., Rueda-Zárate, Héctor A., Noguez, Julieta, Rangel-Escareño, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786538/
https://www.ncbi.nlm.nih.gov/pubmed/31600242
http://dx.doi.org/10.1371/journal.pone.0223183
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author Cárdenas-Ovando, Roberto A.
Fernández-Figueroa, Edith A.
Rueda-Zárate, Héctor A.
Noguez, Julieta
Rangel-Escareño, Claudia
author_facet Cárdenas-Ovando, Roberto A.
Fernández-Figueroa, Edith A.
Rueda-Zárate, Héctor A.
Noguez, Julieta
Rangel-Escareño, Claudia
author_sort Cárdenas-Ovando, Roberto A.
collection PubMed
description Studies conducted in time series could be far more informative than those that only capture a specific moment in time. However, when it comes to transcriptomic data, time points are sparse creating the need for a constant search for methods capable of extracting information out of experiments of this kind. We propose a feature selection algorithm embedded in a hidden Markov model applied to gene expression time course data on either single or even multiple biological conditions. For the latter, in a simple case-control study features or genes are selected under the assumption of no change over time for the control samples, while the case group must have at least one change. The proposed model reduces the feature space according to a two-state hidden Markov model. The two states define change/no-change in gene expression. Features are ranked in consonance with three scores: number of changes across time, magnitude of such changes and quality of replicates as a measure of how much they deviate from the mean. An important highlight is that this strategy overcomes the few samples limitation, common in transcriptome experiments through a process of data transformation and rearrangement. To prove this method, our strategy was applied to three publicly available data sets. Results show that feature domain is reduced by up to 90% leaving only few but relevant features yet with findings consistent to those previously reported. Moreover, our strategy proved to be robust, stable and working on studies where sample size is an issue otherwise. Hence, even with two biological replicates and/or three time points our method proves to work well.
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spelling pubmed-67865382019-10-20 A feature selection strategy for gene expression time series experiments with hidden Markov models Cárdenas-Ovando, Roberto A. Fernández-Figueroa, Edith A. Rueda-Zárate, Héctor A. Noguez, Julieta Rangel-Escareño, Claudia PLoS One Research Article Studies conducted in time series could be far more informative than those that only capture a specific moment in time. However, when it comes to transcriptomic data, time points are sparse creating the need for a constant search for methods capable of extracting information out of experiments of this kind. We propose a feature selection algorithm embedded in a hidden Markov model applied to gene expression time course data on either single or even multiple biological conditions. For the latter, in a simple case-control study features or genes are selected under the assumption of no change over time for the control samples, while the case group must have at least one change. The proposed model reduces the feature space according to a two-state hidden Markov model. The two states define change/no-change in gene expression. Features are ranked in consonance with three scores: number of changes across time, magnitude of such changes and quality of replicates as a measure of how much they deviate from the mean. An important highlight is that this strategy overcomes the few samples limitation, common in transcriptome experiments through a process of data transformation and rearrangement. To prove this method, our strategy was applied to three publicly available data sets. Results show that feature domain is reduced by up to 90% leaving only few but relevant features yet with findings consistent to those previously reported. Moreover, our strategy proved to be robust, stable and working on studies where sample size is an issue otherwise. Hence, even with two biological replicates and/or three time points our method proves to work well. Public Library of Science 2019-10-10 /pmc/articles/PMC6786538/ /pubmed/31600242 http://dx.doi.org/10.1371/journal.pone.0223183 Text en © 2019 Cárdenas-Ovando et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cárdenas-Ovando, Roberto A.
Fernández-Figueroa, Edith A.
Rueda-Zárate, Héctor A.
Noguez, Julieta
Rangel-Escareño, Claudia
A feature selection strategy for gene expression time series experiments with hidden Markov models
title A feature selection strategy for gene expression time series experiments with hidden Markov models
title_full A feature selection strategy for gene expression time series experiments with hidden Markov models
title_fullStr A feature selection strategy for gene expression time series experiments with hidden Markov models
title_full_unstemmed A feature selection strategy for gene expression time series experiments with hidden Markov models
title_short A feature selection strategy for gene expression time series experiments with hidden Markov models
title_sort feature selection strategy for gene expression time series experiments with hidden markov models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786538/
https://www.ncbi.nlm.nih.gov/pubmed/31600242
http://dx.doi.org/10.1371/journal.pone.0223183
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