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PM-Seq: Using Finite Poisson Mixture Models for RNA-Seq Data Analysis and Transcript Expression Level Quantification

机译:PM-Seq:使用有限泊松混合物模型进行RNA-Seq数据分析和转录表达水平定量

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RNA-Seq has emerged as a powerful technique for transcriptome study. As much as the improved sensitivity and coverage, RNA-Seq also brings about challenges for data analysis. The massive amount of sequence reads data, excessive variability, uncertainties, and bias and noises stemming from multiple sources all make the analysis of RNA-Seq data difficult. Despite much progress, RNA-Seq data analysis still has much room for improvement, especially on the quantification of transcript/gene expression levels. In this article, using finite Poisson mixture models, we propose a two-step approach, called PM-Seq, to characterizing base pair level RNA-Seq data and quantifying transcript/gene expression levels. Finite Poisson mixture models combine the strength of fully parametric models with the flexibility of fully nonparametric models, and are extremely suitable for modeling heterogeneous count data such as RNA-Seq data. In particular, we consider three types of Poisson mixture model and propose to use a BIC-based model selection procedure to adapt the models to individual transcripts. A unified quantification method based on the Poisson mixture models is developed to measure transcript/gene expression levels. The Poisson mixture models and the proposed quantification method were applied to analyze two RNA-Seq data sets and demonstrated excellent performances in comparison with other existing methods. Our approach resulted in better characterization of the data and more accurate measurements of transcript expression levels. We believe that finite Poisson mixture models provide a flexible framework to model RNA-Seq data, and methods developed based on this framework have the potential to become powerful tools for RNA-Seq data analysis.
机译:RNA-Seq已成为一种强大的转录组研究技术。除了提高灵敏度和覆盖范围外,RNA-Seq还给数据分析带来了挑战。大量的序列读取数据,过多的变异性,不确定性以及来自多个来源的偏差和噪音,都使RNA-Seq数据分析变得困难。尽管取得了很大进展,但RNA-Seq数据分析仍有很大的改进空间,尤其是在转录本/基因表达水平的定量分析上。在本文中,我们使用有限的Poisson混合模型,提出了一种称为PM-Seq的两步方法来表征碱基对水平的RNA-Seq数据并定量转录本/基因表达水平。有限泊松混合模型将完全参数化模型的优势与完全非参数化模型的灵活性相结合,非常适合于对异构计数数据(例如RNA-Seq数据)进行建模。特别是,我们考虑了三种类型的Poisson混合模型,并建议使用基于BIC的模型选择程序来使模型适应单个笔录。开发了一种基于Poisson混合模型的统一量化方法来测量转录本/基因表达水平。泊松混合模型和拟议的量化方法被用于分析两个RNA-Seq数据集,并证明了与其他现有方法相比的出色性能。我们的方法可以更好地表征数据并更准确地测量转录表达水平。我们相信有限的泊松混合模型提供了一个灵活的框架来对RNA-Seq数据进行建模,并且基于该框架开发的方法有可能成为RNA-Seq数据分析的强大工具。

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