A Novel Bayesian Outlier Score Based on the Negative Binomial Distribution for Detecting Aberrantly Expressed Genes in RNA-Seq Gene Expression Count Data

IF 3.6 3区 计算机科学 Q2 COMPUTER SCIENCE, INFORMATION SYSTEMS IEEE Access Pub Date : 1900-01-01 DOI:10.1109/ACCESS.2021.3082311
Edin Salkovic, H. Bensmail
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引用次数: 2

Abstract

The Negative Binomial distribution (NBD) is used for modeling many types of count data, including gene expression counts obtained by RNA sequencing technologies (RNA-Seq). Finding outliers in this type of data has been shown in recent research to help in identifying rare genetic disorders in humans. Existing Bayesian approaches to detecting outliers in data following the NBD are either computationally inefficient or too general and hence do not leverage the NBD’s specificities in an optimal way. We present a novel Bayesian outlier score for data following the NBD, relying on recent advances in the inference of its dispersion parameter through a special method of Gibbs sampling. The novel Bayesian model on which our score is based — OutPyRX (Outlier detection in Python for RNA-Seq, eXtended version) — improves the model of its predecessor OutPyR by introducing novel parameters that are derived from OutPyR’s. These novel parameters allow more than 6 times faster convergence of the novel outlier score compared to OutPyR’s while having a negligible computational impact on the Gibbs sampling procedure. We show that, in terms of area under precision-recall curve (AUC) values, the novel score outcompetes existing scores on 21 out of 24 datasets that we derived from 4 real datasets by injecting artificial outliers. However, OutPyRX does not perform confounder control which is required for some datasets containing biological outliers. The model is general and can be applied to other similar count data. The code for our model is available at https://github.com/esalkovic/outpyrx.
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基于负二项分布的新型贝叶斯异常值评分在RNA-Seq基因表达计数数据中检测异常表达基因
负二项分布(NBD)用于模拟多种类型的计数数据,包括通过RNA测序技术(RNA- seq)获得的基因表达计数。最近的研究表明,在这类数据中发现异常值有助于识别人类罕见的遗传疾病。现有的贝叶斯方法在NBD之后检测数据中的异常值,要么计算效率低下,要么过于笼统,因此不能以最佳方式利用NBD的特殊性。我们提出了一种新的贝叶斯离群值分数的数据遵循NBD,依靠最近的进展,通过吉布斯抽样的特殊方法推断其离散参数。我们的分数所基于的新型贝叶斯模型——OutPyRX (Python中用于RNA-Seq的离群值检测,扩展版)——通过引入源自OutPyR的新参数,改进了其前身OutPyR的模型。与OutPyR相比,这些新参数可以使新异常值得分的收敛速度提高6倍以上,同时对Gibbs采样过程的计算影响可以忽略不计。我们表明,就精确度召回曲线(AUC)值下的面积而言,新分数在24个数据集中的21个上优于现有分数,这些数据集是我们通过注入人工异常值从4个真实数据集中获得的。然而,OutPyRX不执行混杂控制,这是一些包含生物异常值的数据集所需要的。该模型具有通用性,可应用于其他类似的计数数据。我们的模型的代码可以在https://github.com/esalkovic/outpyrx上找到。
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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来源期刊
IEEE Access
IEEE Access COMPUTER SCIENCE, INFORMATION SYSTEMSENGIN-ENGINEERING, ELECTRICAL & ELECTRONIC
CiteScore
9.80
自引率
7.70%
发文量
6673
审稿时长
6 weeks
期刊介绍: IEEE Access® is a multidisciplinary, open access (OA), applications-oriented, all-electronic archival journal that continuously presents the results of original research or development across all of IEEE''s fields of interest. IEEE Access will publish articles that are of high interest to readers, original, technically correct, and clearly presented. Supported by author publication charges (APC), its hallmarks are a rapid peer review and publication process with open access to all readers. Unlike IEEE''s traditional Transactions or Journals, reviews are "binary", in that reviewers will either Accept or Reject an article in the form it is submitted in order to achieve rapid turnaround. Especially encouraged are submissions on: Multidisciplinary topics, or applications-oriented articles and negative results that do not fit within the scope of IEEE''s traditional journals. Practical articles discussing new experiments or measurement techniques, interesting solutions to engineering. Development of new or improved fabrication or manufacturing techniques. Reviews or survey articles of new or evolving fields oriented to assist others in understanding the new area.
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