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OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data

机译:旁白:一种用于检测RNA测序数据中异常表达基因的统计方法

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摘要

RNA sequencing (RNA-seq) is gaining popularity as a complementary assay to genome sequencing for precisely identifying the molecular causes of rare disorders. A powerful approach is to identify aberrant gene expression levels as potential pathogenic events. However, existing methods for detecting aberrant read counts in RNA-seq data either lack assessments of statistical significance, so that establishing cutoffs is arbitrary, or rely on subjective manual corrections for confounders. Here, we describe OUTRIDER (Outlier in RNA-Seq Finder), an algorithm developed to address these issues. The algorithm uses an autoencoder to model read-count expectations according to the gene covariation resulting from technical, environmental, or common genetic variations. Given these expectations, the RNA-seq read counts are assumed to follow a negative binomial distribution with a gene-specific dispersion. Outliers are then identified as read counts that significantly deviate from this distribution. The model is automatically fitted to achieve the best recall of artificially corrupted data. Precision-recall analyses using simulated outlier read counts demonstrated the importance of controlling for covariation and significance-based thresholds. OUTRIDER is open source and includes functions for filtering out genes not expressed in a dataset, for identifying outlier samples with too many aberrantly expressed genes, and for detecting aberrant gene expression on the basis of false-discovery-rate-adjusted p values. Overall, OUTRIDER provides an end-to-end solution for identifying aberrantly expressed genes and is suitable for use by rare-disease diagnostic platforms.
机译:RNA测序(RNA-seq)作为基因组测序的一种补充检测方法正变得越来越流行,用于精确鉴定罕见疾病的分子原因。一种有效的方法是将异常基因表达水平鉴定为潜在的致病事件。但是,用于检测RNA-seq数据中异常读数计数的现有方法要么缺乏对统计意义的评估,以至于确定临界值是任意的,要么依赖于主观的人工校正。在这里,我们描述了OUTRIDER(RNA-Seq Finder中的离群值),该算法是为解决这些问题而开发的。该算法使用自动编码器,根据技术,环境或常见遗传变异产生的基因协变,对读取期望值进行建模。考虑到这些期望,假定RNA-seq读计数遵循负二项分布,且具有基因特异性分散。然后将异常值识别为与该分布有明显偏差的读取计数。该模型将自动进行拟合,以最佳地调用人为破坏的数据。使用模拟的异常值读取计数进行的精确召回分析表明,控制协变量和基于重要性的阈值的重要性。 OUTRIDER是开放源代码,包括过滤掉数据集中未表达的基因,识别异常表达基因过多的异常样本以及基于错误发现率调整的p值检测异常基因表达的功能。总体而言,OUTRIDER提供了端到端解决方案,用于识别异常表达的基因,适用于罕见病诊断平台。

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