增强的miRNA靶标预测框架

Emad E. Ahmed, Sherin Elgokhy, M. Saidahmed
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引用次数: 0

摘要

MicroRNAs是一种小的非编码RNA分子,在转录后基因调控中起重要作用。它们与信使rna结合,影响导致心脏病和癌症等疾病的基因表达调节。miRNA靶标预测的两种先驱策略要么是实验的,要么是计算的。由于实验技术非常昂贵和缓慢,已经提出了几种计算工具来克服一些实验技术困难。在本文中,我们提出了一个增强的计算框架,该框架根据从miRNA及其靶标的排列中提取的结构、位置和热力学特征来预测miRNA靶标。然后,利用特征的协方差矩阵的特征值分析选择线性可分特征。最后,将选择的特征应用到随机森林分类器中。得到的结果证明,我们的框架明显优于其他现有的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced framework for miRNA target prediction
MicroRNAs are small non-coding RNA molecules that play an important role in post-transcriptional gene regulation. They bind with messenger RNAs, affecting the regulation of gene expression causing diseases such as heart diseases and cancer. The two pioneer strategies of miRNA target prediction are either experimentally or computationally. Since experimental techniques are very expensive and slow, several computational tools have been proposed to defeat some of the experimental technical difficulties. In this paper, we propose an enhanced computational framework that predicts miRNA targets depending on structural, positional, and thermodynamic features extracted from the alignment of miRNA and its targets. Then, we select the linearly separable features using the eigenvalue analysis of the covariance matrix of the features. Finally, the selected features are applied to random forest classifier. The obtained results prove that our framework significantly excels other existing tools.
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