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Modeling Skewness in Human Transcriptomes

Gene expression data are influenced by multiple biological and technological factors leading to a wide range of dispersion scenarios, although skewed patterns are not commonly addressed in microarray analyses. In this study, the distribution pattern of several human transcriptomes has been studied o...

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Detalles Bibliográficos
Autores principales: Casellas, Joaquim, Varona, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372486/
https://www.ncbi.nlm.nih.gov/pubmed/22701729
http://dx.doi.org/10.1371/journal.pone.0038919
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author Casellas, Joaquim
Varona, Luis
author_facet Casellas, Joaquim
Varona, Luis
author_sort Casellas, Joaquim
collection PubMed
description Gene expression data are influenced by multiple biological and technological factors leading to a wide range of dispersion scenarios, although skewed patterns are not commonly addressed in microarray analyses. In this study, the distribution pattern of several human transcriptomes has been studied on free-access microarray gene expression data. Our results showed that, even in previously normalized gene expression data, probe and differential expression within probe effects suffer from substantial departures from the commonly assumed symmetric Gaussian distribution. We developed a flexible mixed model for non-competitive microarray data analysis that accounted for asymmetric and heavy-tailed (Student’s t distribution) dispersion processes. Random effects for gene expression data were modeled under asymmetric Student’s t distributions where the asymmetry parameter (λ) took values from perfect symmetry (λ = 0) to right- (λ>0) or left-side (λ>0) over-expression patterns. This approach was applied to four free-access human data sets and revealed clearly better model performance when comparing with standard approaches accounting for traditional symmetric Gaussian distribution patterns. Our analyses on human gene expression data revealed a substantial degree of right-hand asymmetry for probe effects, whereas differential gene expression addressed both symmetric and left-hand asymmetric patterns. Although these results cannot be extrapolated to all microarray experiments, they highlighted the incidence of skew dispersion patterns in human transcriptome; moreover, we provided a new analytical approach to appropriately address this biological phenomenon. The source code of the program accommodating these analytical developments and additional information about practical aspects on running the program are freely available by request to the corresponding author of this article.
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spelling pubmed-33724862012-06-13 Modeling Skewness in Human Transcriptomes Casellas, Joaquim Varona, Luis PLoS One Research Article Gene expression data are influenced by multiple biological and technological factors leading to a wide range of dispersion scenarios, although skewed patterns are not commonly addressed in microarray analyses. In this study, the distribution pattern of several human transcriptomes has been studied on free-access microarray gene expression data. Our results showed that, even in previously normalized gene expression data, probe and differential expression within probe effects suffer from substantial departures from the commonly assumed symmetric Gaussian distribution. We developed a flexible mixed model for non-competitive microarray data analysis that accounted for asymmetric and heavy-tailed (Student’s t distribution) dispersion processes. Random effects for gene expression data were modeled under asymmetric Student’s t distributions where the asymmetry parameter (λ) took values from perfect symmetry (λ = 0) to right- (λ>0) or left-side (λ>0) over-expression patterns. This approach was applied to four free-access human data sets and revealed clearly better model performance when comparing with standard approaches accounting for traditional symmetric Gaussian distribution patterns. Our analyses on human gene expression data revealed a substantial degree of right-hand asymmetry for probe effects, whereas differential gene expression addressed both symmetric and left-hand asymmetric patterns. Although these results cannot be extrapolated to all microarray experiments, they highlighted the incidence of skew dispersion patterns in human transcriptome; moreover, we provided a new analytical approach to appropriately address this biological phenomenon. The source code of the program accommodating these analytical developments and additional information about practical aspects on running the program are freely available by request to the corresponding author of this article. Public Library of Science 2012-06-11 /pmc/articles/PMC3372486/ /pubmed/22701729 http://dx.doi.org/10.1371/journal.pone.0038919 Text en Casellas, Varona. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Casellas, Joaquim
Varona, Luis
Modeling Skewness in Human Transcriptomes
title Modeling Skewness in Human Transcriptomes
title_full Modeling Skewness in Human Transcriptomes
title_fullStr Modeling Skewness in Human Transcriptomes
title_full_unstemmed Modeling Skewness in Human Transcriptomes
title_short Modeling Skewness in Human Transcriptomes
title_sort modeling skewness in human transcriptomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372486/
https://www.ncbi.nlm.nih.gov/pubmed/22701729
http://dx.doi.org/10.1371/journal.pone.0038919
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