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ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences

BACKGROUND: The recent advances in next generation sequencing technology have made the sequencing of RNA (i.e., RNA-Seq) an extemely popular approach for gene expression analysis. Identification of significant differential expression represents a crucial initial step in these analyses, on which most...

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Autores principales: Yang, Wentao, Rosenstiel, Philip C., Schulenburg, Hinrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973090/
https://www.ncbi.nlm.nih.gov/pubmed/27488180
http://dx.doi.org/10.1186/s12864-016-2848-2
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author Yang, Wentao
Rosenstiel, Philip C.
Schulenburg, Hinrich
author_facet Yang, Wentao
Rosenstiel, Philip C.
Schulenburg, Hinrich
author_sort Yang, Wentao
collection PubMed
description BACKGROUND: The recent advances in next generation sequencing technology have made the sequencing of RNA (i.e., RNA-Seq) an extemely popular approach for gene expression analysis. Identification of significant differential expression represents a crucial initial step in these analyses, on which most subsequent inferences of biological functions are built. Yet, for identification of these subsequently analysed genes, most studies use an additional minimal threshold of differential expression that is not captured by the applied statistical procedures. RESULTS: Here we introduce a new analysis approach, ABSSeq, which uses a negative binomal distribution to model absolute expression differences between conditions, taking into account variations across genes and samples as well as magnitude of differences. In comparison to alternative methods, ABSSeq shows higher performance on controling type I error rate and at least a similar ability to correctly identify differentially expressed genes. CONCLUSIONS: ABSSeq specifically considers the overall magnitude of expression differences, which enhances the power in detecting truly differentially expressed genes by reducing false positives at both very low and high expression level. In addition, ABSSeq offers to calculate shrinkage of fold change to facilitate gene ranking and effective outlier detection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2848-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-49730902016-08-05 ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences Yang, Wentao Rosenstiel, Philip C. Schulenburg, Hinrich BMC Genomics Software BACKGROUND: The recent advances in next generation sequencing technology have made the sequencing of RNA (i.e., RNA-Seq) an extemely popular approach for gene expression analysis. Identification of significant differential expression represents a crucial initial step in these analyses, on which most subsequent inferences of biological functions are built. Yet, for identification of these subsequently analysed genes, most studies use an additional minimal threshold of differential expression that is not captured by the applied statistical procedures. RESULTS: Here we introduce a new analysis approach, ABSSeq, which uses a negative binomal distribution to model absolute expression differences between conditions, taking into account variations across genes and samples as well as magnitude of differences. In comparison to alternative methods, ABSSeq shows higher performance on controling type I error rate and at least a similar ability to correctly identify differentially expressed genes. CONCLUSIONS: ABSSeq specifically considers the overall magnitude of expression differences, which enhances the power in detecting truly differentially expressed genes by reducing false positives at both very low and high expression level. In addition, ABSSeq offers to calculate shrinkage of fold change to facilitate gene ranking and effective outlier detection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2848-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-04 /pmc/articles/PMC4973090/ /pubmed/27488180 http://dx.doi.org/10.1186/s12864-016-2848-2 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Yang, Wentao
Rosenstiel, Philip C.
Schulenburg, Hinrich
ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title_full ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title_fullStr ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title_full_unstemmed ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title_short ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences
title_sort absseq: a new rna-seq analysis method based on modelling absolute expression differences
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973090/
https://www.ncbi.nlm.nih.gov/pubmed/27488180
http://dx.doi.org/10.1186/s12864-016-2848-2
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