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Consensus RNA secondary structure prediction based on SVMs

机译:基于支持向量机的共识RNA二级结构预测

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Although many endeavors have been done in the field of RNA secondary structure prediction, it is still an open problem in the computational molecular biology. The comparative sequence analysis is the golden standard method when given homologous sequence alignment. The essential of this method can be regarded as classifier problem: to judge whether any two columns of an alignment correspond to a base pair using provided information by alignment. Here, we employ SVMs to resolve this classifier problem, and select the covaration score, the fraction of complementary nucleotides and the consensus probability matrix as the feature vectors. Test on the Rfam shows that average MCC of our method is higher (0.841) than KnetFold (0.831), Pfold (0.741) and RNAalifold(0.623).
机译:尽管在RNA二级结构预测领域已经进行了许多努力,但是在计算分子生物学中它仍然是一个未解决的问题。当进行同源序列比对时,比较序列分析是黄金标准方法。该方法的本质可以视为分类器问题:使用比对提供的信息来判断比对的任何两列是否对应于碱基对。在这里,我们使用支持向量机来解决该分类器问题,并选择共变分数,互补核苷酸的分数和共识概率矩阵作为特征向量。对Rfam进行的测试表明,我们的方法的平均MCC值(0.841)高于KnetFold(0.831),Pfold(0.741)和RNAalifold(0.623)。

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