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A new shrinkage estimator for dispersion improves differential expression detection in RNA-seq data

机译:一种用于分散的新的收缩估算器可改善RNA序列数据中的差异表达检测

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Recent developments in RNA-sequencing (RNA-seq) technology have led to a rapid increase in gene expression data in the form of counts. RNA-seq can be used for a variety of applications, however, identifying differential expression (DE) remains a key task in functional genomics. There have been a number of statistical methods for DE detection for RNA-seq data. One common feature of several leading methods is the use of the negative binomial (Gamma-Poisson mixture) model. That is, the unobserved gene expression is modeled by a gamma random variable and, given the expression, the sequencing read counts are modeled as Poisson. The distinct feature in various methods is how the variance, or dispersion, in the Gamma distribution is modeled and estimated. We evaluate several large public RNA-seq datasets and find that the estimated dispersion in existing methods does not adequately capture the heterogeneity of biological variance among samples. We present a new empirical Bayes shrinkage estimate of the dispersion parameters and demonstrate improved DE detection.
机译:RNA测序(RNA-seq)技术的最新发展已导致计数形式的基因表达数据迅速增加。 RNA-seq可用于多种应用,但是,鉴定差异表达(DE)仍然是功能基因组学中的关键任务。已经有许多用于DE检测RNA-seq数据的统计方法。几种主要方法的一个共同特征是使用负二项式(伽玛-泊松混合)模型。也就是说,未观察到的基因表达是由伽马随机变量建模的,给定该表达,测序读取计数被建模为泊松。各种方法的不同之处在于如何对Gamma分布中的方差或离散进行建模和估计。我们评估了几个大型公共RNA-seq数据集,发现在现有方法中估计的分散度不能充分捕获样品之间生物差异的异质性。我们提出了色散参数的新的经验贝叶斯收缩估计,并演示了改进的DE检测。

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