Detecting differential expression in RNA-sequence data using quasi-likelihood with shrunken dispersion estimates.

Pub Date : 2012-10-22 DOI:10.1515/1544-6115.1826
Steven P Lund, Dan Nettleton, Davis J McCarthy, Gordon K Smyth
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引用次数: 280

Abstract

Next generation sequencing technology provides a powerful tool for measuring gene expression (mRNA) levels in the form of RNA-sequence data. Method development for identifying differentially expressed (DE) genes from RNA-seq data, which frequently includes many low-count integers and can exhibit severe overdispersion relative to Poisson or binomial distributions, is a popular area of ongoing research. Here we present quasi-likelihood methods with shrunken dispersion estimates based on an adaptation of Smyth's (2004) approach to estimating gene-specific error variances for microarray data. Our suggested methods are computationally simple, analogous to ANOVA and compare favorably versus competing methods in detecting DE genes and estimating false discovery rates across a variety of simulations based on real data.

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利用准似然和缩小的分散估计检测rna序列数据中的差异表达。
下一代测序技术以rna序列数据的形式为测量基因表达(mRNA)水平提供了强大的工具。从RNA-seq数据中识别差异表达(DE)基因的方法开发是一个正在进行的热门研究领域,这些基因通常包括许多低计数整数,并且相对于泊松分布或二项分布可能表现出严重的过分散。在这里,我们提出了基于Smyth(2004)方法的准似然方法,缩小了分散估计,用于估计微阵列数据的基因特异性误差方差。我们建议的方法计算简单,类似于方差分析,并且在检测DE基因和估计基于真实数据的各种模拟的错误发现率方面优于竞争方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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