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reactIDR: evaluation of the statistical reproducibility of high-throughput structural analyses towards a robust RNA structure prediction

机译:ReactIDR:评估高通量结构分析朝向鲁棒RNA结构预测的统计再现性

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Recently, next-generation sequencing techniques have been applied for the detection of RNA secondary structures, which is referred to as high-throughput RNA structural (HTS) analyses, and many different protocols have been used to detect comprehensive RNA structures at single-nucleotide resolution. However, the existing computational analyses heavily depend on the experimental methodology to generate data, which results in difficulties associated with statistically sound comparisons or combining the results obtained using different HTS methods. Here, we introduced a statistical framework, reactIDR, which can be applied to the experimental data obtained using multiple HTS methodologies. Using this approach, nucleotides are classified into three structural categories, loop, stem/background, and unmapped. reactIDR uses the irreproducible discovery rate (IDR) with a hidden Markov model to discriminate between the true and spurious signals obtained in the replicated HTS experiments accurately, and it is able to incorporate an expectation-maximization algorithm and supervised learning for efficient parameter optimization. The results of our analyses of the real-life HTS data showed that reactIDR had the highest accuracy in the classification of ribosomal RNA stem/loop structures when using both individual and integrated HTS datasets, and its results corresponded the best to the three-dimensional structures. We have developed a novel software, reactIDR, for the prediction of stem/loop regions from the HTS analysis datasets. For the rRNA structure analyses, reactIDR was shown to have robust accuracy across different datasets by using the reproducibility criterion, suggesting its potential for increasing the value of existing HTS datasets. reactIDR is publicly available at https://github.com/carushi/reactIDR .
机译:最近,已经施加下一代测序技术用于检测RNA二级结构,其被称为高通量RNA结构(HTS)分析,并且许多不同的方案已经用于以单核苷酸分辨率检测综合的RNA结构。然而,现有的计算分析严重依赖于生成数据的实验方法,这导致与统计学声音比较相关的困难或组合使用不同HTS方法获得的结果。在这里,我们介绍了一种统计框架,反应器,其可以应用于使用多个HTS方法获得的实验数据。使用这种方法,核苷酸分为三个结构类别,环路,茎/背景和未映射。 ReactIDR使用带有隐藏的Markov模型的IrreoProocue发现率(IDR),以准确地区分在复制的HTS实验中获得的真实和虚假信号,并且能够结合期望最大化算法和监督学习以获得有效参数优化。我们对现实寿命HTS数据分析的结果表明,当使用单个单独的HTS数据集时,ReactIDR在核糖体RNA茎/环结构的分类中具有最高的精度,其结果与三维结构相对应。我们开发了一种新颖的软件,反弹,用于预测HTS分析数据集的阀杆/环路区域。对于RRNA结构分析,通过使用再现性标准,ReactIDR显示跨不同数据集的鲁棒精度,表明其增加现有HTS数据集的潜力。 ReactIDR在https://github.com/carushi/reacctidr公开使用。

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