Evidence map›Paper›PMID 31600242›Full record

ArticlePloS one2019

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

Roberto A Cárdenas-Ovando, Edith A Fernández-Figueroa, Héctor A Rueda-Zárate, Julieta Noguez, Claudia Rangel-Escareño

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Roberto A Cárdenas-OvandoSchool of Engineering and Sciences, Tecnológico de Monterrey, Mexico City, Mexico.ORCID 0000-0002-8261-1037
Edith A Fernández-FigueroaComputational Genomics Lab, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.ORCID 0000-0002-5159-8300
Héctor A Rueda-ZárateSchool of Engineering and Sciences, Tecnológico de Monterrey, Mexico City, Mexico.
Julieta NoguezSchool of Engineering and Sciences, Tecnológico de Monterrey, Mexico City, Mexico.ORCID 0000-0002-6000-3452
Claudia Rangel-EscareñoComputational Genomics Lab, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.ORCID 0000-0003-1303-0834

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Markov ChainsModels, StatisticalAlgorithmsCase-Control StudiesGene Expression

Identifiers

PMID31600242
PMCPMC6786538

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.