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Negative binomial additive model for RNA-Seq data analysis

BACKGROUND: High-throughput sequencing experiments followed by differential expression analysis is a widely used approach for detecting genomic biomarkers. A fundamental step in differential expression analysis is to model the association between gene counts and covariates of interest. Existing mode...

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Autores principales: Ren, Xu, Kuan, Pei-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195715/
https://www.ncbi.nlm.nih.gov/pubmed/32357831
http://dx.doi.org/10.1186/s12859-020-3506-x
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author Ren, Xu
Kuan, Pei-Fen
author_facet Ren, Xu
Kuan, Pei-Fen
author_sort Ren, Xu
collection PubMed
description BACKGROUND: High-throughput sequencing experiments followed by differential expression analysis is a widely used approach for detecting genomic biomarkers. A fundamental step in differential expression analysis is to model the association between gene counts and covariates of interest. Existing models assume linear effect of covariates, which is restrictive and may not be sufficient for certain phenotypes. RESULTS: We introduce NBAMSeq, a flexible statistical model based on the generalized additive model and allows for information sharing across genes in variance estimation. Specifically, we model the logarithm of mean gene counts as sums of smooth functions with the smoothing parameters and coefficients estimated simultaneously within a nested iterative method. The variance is estimated by the Bayesian shrinkage approach to fully exploit the information across all genes. CONCLUSIONS: Based on extensive simulations and case studies of RNA-Seq data, we show that NBAMSeq offers improved performance in detecting nonlinear effect and maintains equivalent performance in detecting linear effect compared to existing methods. The vignette and source code of NBAMSeq are available at http://bioconductor.org/packages/release/bioc/html/NBAMSeq.html.
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spelling pubmed-71957152020-05-06 Negative binomial additive model for RNA-Seq data analysis Ren, Xu Kuan, Pei-Fen BMC Bioinformatics Software BACKGROUND: High-throughput sequencing experiments followed by differential expression analysis is a widely used approach for detecting genomic biomarkers. A fundamental step in differential expression analysis is to model the association between gene counts and covariates of interest. Existing models assume linear effect of covariates, which is restrictive and may not be sufficient for certain phenotypes. RESULTS: We introduce NBAMSeq, a flexible statistical model based on the generalized additive model and allows for information sharing across genes in variance estimation. Specifically, we model the logarithm of mean gene counts as sums of smooth functions with the smoothing parameters and coefficients estimated simultaneously within a nested iterative method. The variance is estimated by the Bayesian shrinkage approach to fully exploit the information across all genes. CONCLUSIONS: Based on extensive simulations and case studies of RNA-Seq data, we show that NBAMSeq offers improved performance in detecting nonlinear effect and maintains equivalent performance in detecting linear effect compared to existing methods. The vignette and source code of NBAMSeq are available at http://bioconductor.org/packages/release/bioc/html/NBAMSeq.html. BioMed Central 2020-05-01 /pmc/articles/PMC7195715/ /pubmed/32357831 http://dx.doi.org/10.1186/s12859-020-3506-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Software
Ren, Xu
Kuan, Pei-Fen
Negative binomial additive model for RNA-Seq data analysis
title Negative binomial additive model for RNA-Seq data analysis
title_full Negative binomial additive model for RNA-Seq data analysis
title_fullStr Negative binomial additive model for RNA-Seq data analysis
title_full_unstemmed Negative binomial additive model for RNA-Seq data analysis
title_short Negative binomial additive model for RNA-Seq data analysis
title_sort negative binomial additive model for rna-seq data analysis
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195715/
https://www.ncbi.nlm.nih.gov/pubmed/32357831
http://dx.doi.org/10.1186/s12859-020-3506-x
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