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Predicting Human miRNA Target Genes Using a Novel Evolutionary Methodology

机译:使用新型进化方法预测人类miRNA靶基因

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The discovery of miRNAs had great impacts on traditional biology. Typically, miRNAs have the potential to bind to the 3'untraslated region (UTR) of their mRNA target genes for cleavage or translational repression. The experimental identification of their targets has many drawbacks including cost, time and low specificity and these are the reasons why many computational approaches have been developed so far. However, existing computational approaches do not include any advanced feature selection technique and they are facing problems concerning their classification performance and their interpre-tability. In the present paper, we propose a novel hybrid methodology which combines genetic algorithms and support vector machines in order to locate the optimal feature subset while achieving high classification performance. The proposed methodology was compared with two of the most promising existing methodologies in the problem of predicting human miRNA targets. Our approach outperforms existing methodologies in terms of classification performances while selecting a much smaller feature subset.
机译:miRNA的发现对传统生物学产生了巨大影响。通常,miRNA有可能与其mRNA靶基因的3'未修饰区域(UTR)结合,以进行切割或翻译抑制。对目标物的实验鉴定具有许多缺点,包括成本,时间和特异性低,这些都是迄今为止开发出许多计算方法的原因。然而,现有的计算方法不包括任何高级特征选择技术,并且它们面临有关其分类性能和可解释性的问题。在本文中,我们提出了一种新颖的混合方法,该方法结合了遗传算法和支持向量机,以便在实现高分类性能的同时定位最佳特征子集。在预测人类miRNA目标的问题上,将所提出的方法与两种最有前途的现有方法进行了比较。我们的方法在分类性能方面优于现有方法,同时选择了更小的特征子集。

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