4.6 Article

NPEBseq: nonparametric empirical bayesian-based procedure for differential expression analysis of RNA-seq data

Journal

BMC BIOINFORMATICS
Volume 14, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/1471-2105-14-262

Keywords

-

Funding

  1. Commonwealth Universal Research Enhancement (CURE) Research Program, Department of Health, Pennsylvania
  2. Philadelphia Healthcare Trust Endowed Chair Position
  3. National Library Of Medicine of the National Institutes of Health [R01LM011297]
  4. Bioinformatics Shared Facility of Wistar Cancer Centre [P30 CA010815]
  5. NATIONAL CANCER INSTITUTE [P30CA010815] Funding Source: NIH RePORTER
  6. NATIONAL LIBRARY OF MEDICINE [R01LM011297] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Background: RNA-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. Results: We 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. Conclusions: NPEBseq 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available