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voom: precision weights unlock linear model analysis tools for RNA-seq read counts

New normal linear modeling strategies are presented for analyzing read counts from RNA-seq experiments. The voom method estimates the mean-variance relationship of the log-counts, generates a precision weight for each observation and enters these into the limma empirical Bayes analysis pipeline. Thi...

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Detalles Bibliográficos
Autores principales: Law, Charity W, Chen, Yunshun, Shi, Wei, Smyth, Gordon K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053721/
https://www.ncbi.nlm.nih.gov/pubmed/24485249
http://dx.doi.org/10.1186/gb-2014-15-2-r29
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author Law, Charity W
Chen, Yunshun
Shi, Wei
Smyth, Gordon K
author_facet Law, Charity W
Chen, Yunshun
Shi, Wei
Smyth, Gordon K
author_sort Law, Charity W
collection PubMed
description New normal linear modeling strategies are presented for analyzing read counts from RNA-seq experiments. The voom method estimates the mean-variance relationship of the log-counts, generates a precision weight for each observation and enters these into the limma empirical Bayes analysis pipeline. This opens access for RNA-seq analysts to a large body of methodology developed for microarrays. Simulation studies show that voom performs as well or better than count-based RNA-seq methods even when the data are generated according to the assumptions of the earlier methods. Two case studies illustrate the use of linear modeling and gene set testing methods.
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spelling pubmed-40537212014-06-12 voom: precision weights unlock linear model analysis tools for RNA-seq read counts Law, Charity W Chen, Yunshun Shi, Wei Smyth, Gordon K Genome Biol Method New normal linear modeling strategies are presented for analyzing read counts from RNA-seq experiments. The voom method estimates the mean-variance relationship of the log-counts, generates a precision weight for each observation and enters these into the limma empirical Bayes analysis pipeline. This opens access for RNA-seq analysts to a large body of methodology developed for microarrays. Simulation studies show that voom performs as well or better than count-based RNA-seq methods even when the data are generated according to the assumptions of the earlier methods. Two case studies illustrate the use of linear modeling and gene set testing methods. BioMed Central 2014 2014-02-03 /pmc/articles/PMC4053721/ /pubmed/24485249 http://dx.doi.org/10.1186/gb-2014-15-2-r29 Text en Copyright © 2014 Law et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Method
Law, Charity W
Chen, Yunshun
Shi, Wei
Smyth, Gordon K
voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title_full voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title_fullStr voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title_full_unstemmed voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title_short voom: precision weights unlock linear model analysis tools for RNA-seq read counts
title_sort voom: precision weights unlock linear model analysis tools for rna-seq read counts
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053721/
https://www.ncbi.nlm.nih.gov/pubmed/24485249
http://dx.doi.org/10.1186/gb-2014-15-2-r29
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