Abstract

High-throughput sequencing of transcriptomes (RNA-Seq) has recently become a powerful tool for the study of gene expression. We present rSeqDiff, an efficient algorithm for the detection of differential expression and differential splicing of genes from RNA-Seq experiments across multiple conditions. Unlike existing approaches which detect differential expression of transcripts, our approach considers three cases for each gene: 1) no differential expression, 2) differential expression without differential splicing and 3) differential splicing. We specify statistical models characterizing each of these three cases and use hierarchical likelihood ratio test for model selection. Simulation studies show that our approach achieves good power for detecting differentially expressed or differentially spliced genes. Comparisons with competing methods on two real RNA-Seq datasets demonstrate that our approach provides accurate estimates of isoform abundances and biological meaningful rankings of differentially spliced genes. The proposed approach is implemented as an R package named rSeqDiff.

Highlights

  • Alternative splicing is an important mechanism in posttranscriptional regulation of eukaryotes

  • Simulation studies We study the performance of our proposed hierarchical likelihood ratio test (hLRT) approach by simulating read counts from genes with a wide range of abundances and report the specificity and sensitivity of our approach for the detection of differential expression and differential splicing events

  • For each of the three models, we vary the expression level of the gene within a broad range, and for each G we simulate the number of reads mapped to each of the two isoforms according to the three models (equations (2), (3) and (4))

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Summary

Introduction

Alternative splicing is an important mechanism in posttranscriptional regulation of eukaryotes. Due to its vital role in biological processes such as gene regulation, cell differentiation, development and disease pathophysiology, there is an urgent need for the development of new technologies and methodologies for the study of alternative splicing events and the quantification of the expression of alternative isoforms. High-throughput sequencing of transcriptomes (RNA-Seq) has rapidly evolved as a powerful tool for the study of alternative splicing in humans and model organisms [1,2,3,7]. The other type of approach is isoform-based, which focuses on the estimation of differential expression of isoforms across different biological conditions [12,13,14,15,16]

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