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Detecting and Assessing Conserved Stems for Accurate Structural Alignment of RNA Sequences

机译:检测和评估保守茎,用于准确结构对准RNA序列

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Since comparative sequence analysis is effective for non-coding RNA detection and RNA secondary structure prediction, efficient computational methods are expected for structural alignment of RNA sequences. However, it is very difficult to construct awell structural alignment without knowing the secondary structures. In this paper, we present a new method for constructing structural alignment of RNA sequences by detecting and assessing conserved stems. The method can be summarized by: 1) we detect conserved stems across multiple RNA sequences using the so-called position matrix with which some common paired positions are uncovered; 2) we assess the conserved stems using the Signal-to-Noise; 3) we build the structural alignment by incorporating somecompatible conserved stems with the initial sequence alignment constructed by Clustal W program. We tested our method on the data sets composed of known structural alignments taken from the Rfam database. Experimental results show that our method can build structural alignment of RNA sequences with much greater sensitivity and specificity than Clustal W.
机译:由于对比序列分析对于非编码RNA检测和RNA二次结构预测有效,因此预期RNA序列的结构对准的有效计算方法。然而,在不知道二次结构的情况下,非常困难地构建令人讨厌的结构对准。在本文中,我们介绍了一种通过检测和评估保守茎来构建RNA序列的结构对准的新方法。该方法可以概括为:1)通过使用所谓的位置矩阵,我们检测跨多个RNA序列横跨多个RNA序列的茎。 2)我们使用信号对噪声评估保守的茎; 3)我们通过用Clustal W程序构建的初始序列对准来构建结构对准。我们在由RFAM数据库中取出的已知结构对齐组成的数据集上测试了我们的方法。实验结果表明,我们的方法可以构建RNA序列的结构对准,比群集W更大的敏感性和特异性。

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