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Predicting RNA Secondary Structure Using Profile Stochastic Context-Free Grammars and Phylogenic Analysis

机译:使用配置文件随机上下文无关文法和系统发育分析预测RNA二级结构

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Stochastic context-free grammars (SCFGs) have been applied to predicting RNA secondary structure. The prediction of RNA secondary structure can be facilitated by incorporating with comparative sequence analysis. However, most of existing SCFG-based methods lack explicit phylogenic analysis of homologous RNA sequences, which is probably the reason why these methods are not ideal in practical application. Hence, we present a new SCFG-based method by integrating phylogenic analysis with the newly defined profile SCFG. The method can be summarized as: 1) we define a new profile SCFG, M, to depict consensus secondary structure of multiple RNA sequence alignment; 2) we introduce two distinct hidden Markov models, A and A', to perform phylogenic analysis of homologous RNA sequences. Here, A is for non-structural regions of the sequence and A' is for structural regions of the sequence; 3) we merge A and A' into M to devise a combined model for prediction of RNA secondary structure. We tested our method on data sets constructed from the Rfam database. The sensitivity and specificity of our method are more accurate than those of the predictions by Pfold.
机译:随机上下文无关文法(SCFG)已应用于预测RNA二级结构。通过结合比较序列分析可以促进RNA二级结构的预测。但是,大多数现有的基于SCFG的方法都缺乏对同源RNA序列的明确系统发育分析,这可能是这些方法在实际应用中不理想的原因。因此,我们通过将系统发育分析与新定义的配置文件SCFG集成在一起,提出了一种基于SCFG的新方法。该方法可以概括为:1)我们定义了一个新的SCFG图谱M,以描述多个RNA序列比对的共有二级结构; 2)我们引入两个不同的隐马尔可夫模型A和A',以进行同源RNA序列的系统发育分析。在此,A表示序列的非结构区域,A’表示序列的结构区域。 3)我们将A和A'合并为M,以设计一个组合模型来预测RNA二级结构。我们在Rfam数据库构建的数据集上测试了我们的方法。我们的方法的敏感性和特异性比Pfold的预测更为准确。

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