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Consensus RNA secondary structure prediction using information of neighbouring columns and principal component analysis

机译:共识RNA二次结构预测使用邻柱和主成分分析的信息

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摘要

RNA is a family of biological macromolecules. It is important to all kinds of biological processes. RNA structure is closely related to its functions. Hence, determining the structure is invaluable in understanding genetic diseases and creating drugs. Nowadays, RNA secondary structure prediction is a field yet to be researched. In this paper, we present a novel method using RNA sequence alignment to predict a consensus RNA secondary structure. In essence, the goal of the method is to give a prediction about whether any two columns of an alignment correspond to a base pair or not, using the information provided by the alignment. The information includes the covariation score, the fraction of complementary nucleotides and the consensus probability matrix of the column pair and those of its neighbours. Then principal component analysis is applied to overcome the problem of over-fitting. A comparison of our method and other consensus RNA secondary structure prediction methods including NeCFold, ELMFold, KnetFold, PFold and RNAalifold, in 47 families from Rfam (version 11.0) is performed. Results show that our method surpasses the other methods in terms of Matthews correlation coefficient, sensitivity and selectivity.
机译:RNA是一家生物大分子。它对各种生物过程很重要。 RNA结构与其功能密切相关。因此,确定结构在理解遗传疾病和创造药物方面是非常宝贵的。如今,RNA二级结构预测是尚未研究的领域。在本文中,我们介绍了一种使用RNA序列对准的新方法,以预测共有的RNA二级结构。从本质上讲,该方法的目的是通过通过对准提供的信息,给出关于对准是否对对对应的任何两列对应的任何两列对应的预测。该信息包括协变度,互补核苷酸的分数和柱对的共识概率基质和其邻居的分数。然后应用主成分分析来克服过度拟合的问题。进行了来自RFAM(版本11.0)的47个家庭的NeCold,Elmfold,Knetfold,Pfold和Rnaalifold的方法和其他共识RNA二级结构预测方法的比较。结果表明,我们的方法在马修斯相关系数,灵敏度和选择性方面超越了其他方法。

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