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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Main Authors: Roberto A Cárdenas-Ovando, Edith A Fernández-Figueroa, Héctor A Rueda-Zárate, Julieta Noguez, Claudia Rangel-Escareño
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0223183
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spelling doaj-19decaf81ac845be9e187a6b5893fa6e2021-03-03T21:10:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011410e022318310.1371/journal.pone.0223183A feature selection strategy for gene expression time series experiments with hidden Markov models.Roberto A Cárdenas-OvandoEdith A Fernández-FigueroaHéctor A Rueda-ZárateJulieta NoguezClaudia Rangel-EscareñoStudies 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.https://doi.org/10.1371/journal.pone.0223183
collection DOAJ
language English
format Article
sources DOAJ
author Roberto A Cárdenas-Ovando
Edith A Fernández-Figueroa
Héctor A Rueda-Zárate
Julieta Noguez
Claudia Rangel-Escareño
spellingShingle Roberto A Cárdenas-Ovando
Edith A Fernández-Figueroa
Héctor A Rueda-Zárate
Julieta Noguez
Claudia Rangel-Escareño
A feature selection strategy for gene expression time series experiments with hidden Markov models.
PLoS ONE
author_facet Roberto A Cárdenas-Ovando
Edith A Fernández-Figueroa
Héctor A Rueda-Zárate
Julieta Noguez
Claudia Rangel-Escareño
author_sort Roberto A Cárdenas-Ovando
title 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_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_sort feature selection strategy for gene expression time series experiments with hidden markov models.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
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.
url https://doi.org/10.1371/journal.pone.0223183
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