ArticleBMC bioinformatics2013
NPEBseq: nonparametric empirical bayesian-based procedure for differential expression analysis of RNA-seq data.
Article in BMC bioinformatics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Identification of a novel regulatory pathway for PPARα by RNA-seq characterization of the endothelial cell lipid peroxidative injury transcriptome.Open biology · 2019Article
- Optimization of an RNA-Seq Differential Gene Expression Analysis Depending on Biological Replicate Number and Library Size.Frontiers in plant science · 2018Article
- Modeling bias and variation in the stochastic processes of small RNA sequencing.Nucleic acids research · 2017Article
- A survey of best practices for RNA-seq data analysis.Genome biology · 2016Review
- Data quality aware analysis of differential expression in RNA-seq with NOISeq R/Bioc package.Nucleic acids research · 2015Article
- Evaluation of methods for differential expression analysis on multi-group RNA-seq count data.BMC bioinformatics · 2015Article
- Getting the most out of RNA-seq data analysis.PeerJ · 2015Article
- Dynamics in Transcriptomics: Advancements in RNA-seq Time Course and Downstream Analysis.Computational and structural biotechnology journal · 2015Review
- Emerging bioinformatics approaches for analysis of NGS-derived coding and non-coding RNAs in neurodegenerative diseases.Frontiers in cellular neuroscience · 2014Article
- Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.Genome biology · 2014Article
- Bootstrap-based differential gene expression analysis for RNA-Seq data with and without replicates.BMC genomics · 2014Article
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2 authors.
Funding
Abstract
backgroundRNA-seq, a massive parallel-sequencing-based transcriptome profiling method, provides digital data in the form of aligned sequence read counts. The comparative analyses of the data require appropriate statistical methods to estimate the differential expression of transcript variants across different cell/tissue types and disease conditions.
resultsWe developed a novel nonparametric empirical Bayesian-based approach (NPEBseq) to model the RNA-seq data. The prior distribution of the Bayesian model is empirically estimated from the data without any parametric assumption, and hence the method is "nonparametric" in nature. Based on this model, we proposed a method for detecting differentially expressed genes across different conditions. We also extended this method to detect differential usage of exons from RNA-seq data. The evaluation of NPEBseq on both simulated and publicly available RNA-seq datasets and comparison with three popular methods showed improved results for experiments with or without biological replicates.
conclusionsNPEBseq can successfully detect differential expression between different conditions not only at gene level but also at exon level from RNA-seq datasets. In addition, NPEBSeq performs significantly better than current methods and can be applied to genome-wide RNA-seq datasets. Sample datasets and R package are available at http://bioinformatics.wistar.upenn.edu/NPEBseq.
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