DifferentialRegulation: a Bayesian hierarchical approach to identify differentially regulated genes.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Simone Tiberi, Joël Meili, Peiying Cai, Charlotte Soneson, Dongze He, Hirak Sarkar, Alejandra Avalos-Pacheco, Rob Patro, Mark D Robinson
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引用次数: 0

Abstract

Although transcriptomics data is typically used to analyze mature spliced mRNA, recent attention has focused on jointly investigating spliced and unspliced (or precursor-) mRNA, which can be used to study gene regulation and changes in gene expression production. Nonetheless, most methods for spliced/unspliced inference (such as RNA velocity tools) focus on individual samples, and rarely allow comparisons between groups of samples (e.g. healthy vs. diseased). Furthermore, this kind of inference is challenging, because spliced and unspliced mRNA abundance is characterized by a high degree of quantification uncertainty, due to the prevalence of multi-mapping reads, ie reads compatible with multiple transcripts (or genes), and/or with both their spliced and unspliced versions. Here, we present DifferentialRegulation, a Bayesian hierarchical method to discover changes between experimental conditions with respect to the relative abundance of unspliced mRNA (over the total mRNA). We model the quantification uncertainty via a latent variable approach, where reads are allocated to their gene/transcript of origin, and to the respective splice version. We designed several benchmarks where our approach shows good performance, in terms of sensitivity and error control, vs. state-of-the-art competitors. Importantly, our tool is flexible, and works with both bulk and single-cell RNA-sequencing data. DifferentialRegulation is distributed as a Bioconductor R package.

DifferentialRegulation:一种贝叶斯分层方法,用于识别差异调控基因。
虽然转录组学数据通常用于分析成熟剪接的 mRNA,但最近的研究重点是联合研究剪接和未剪接(或前体)的 mRNA,这可用于研究基因调控和基因表达生成的变化。然而,大多数剪接/未剪接推断方法(如 RNA 速度工具)都侧重于单个样本,很少允许在样本组(如健康样本与患病样本)之间进行比较。此外,这种推断具有挑战性,因为剪接和非剪接的 mRNA 丰度具有高度的定量不确定性,这是由于多映射读数(即与多个转录本(或基因)兼容的读数,和/或与它们的剪接和非剪接版本兼容的读数)的普遍存在。在此,我们介绍一种贝叶斯分层方法 DifferentialRegulation,用于发现不同实验条件下未剪接 mRNA(相对于总 mRNA)相对丰度的变化。我们通过潜变量方法对量化的不确定性进行建模,将读数分配到其源基因/转录本以及各自的剪接版本。我们设计了几个基准,与最先进的竞争对手相比,我们的方法在灵敏度和误差控制方面表现出色。重要的是,我们的工具非常灵活,既能处理大容量数据,也能处理单细胞 RNA 序列数据。DifferentialRegulation 以 Bioconductor R 软件包的形式发布。
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
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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