A statistical method for detecting differentially expressed SNVs based on next-generation RNA-seq data

Biometrics. 2017 Mar;73(1):42-51. doi: 10.1111/biom.12548. Epub 2016 Jun 8.

Abstract

In this article, we propose a new statistical method-MutRSeq-for detecting differentially expressed single nucleotide variants (SNVs) based on RNA-seq data. Specifically, we focus on nonsynonymous mutations and employ a hierarchical likelihood approach to jointly model observed mutation events as well as read count measurements from RNA-seq experiments. We then introduce a likelihood ratio-based test statistic, which detects changes not only in overall expression levels, but also in allele-specific expression patterns. In addition, this method can jointly test multiple mutations in one gene/pathway. The simulation studies suggest that the proposed method achieves better power than a few competitors under a range of different settings. In the end, we apply this method to a breast cancer data set and identify genes with nonsynonymous mutations differentially expressed between the triple negative breast cancer tumors and other subtypes of breast cancer tumors.

Keywords: Allele-specific expression; Breast cancer tumors; Differential expression; Likelihood ratio test; RNA-seq.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Breast Neoplasms / classification
  • Breast Neoplasms / genetics
  • Female
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Likelihood Functions
  • Models, Statistical*
  • Mutation
  • Polymorphism, Single Nucleotide / genetics*
  • Sequence Analysis, RNA / methods
  • Software