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Feature Selection Combined with Neural Network Structure Optimization for HIV-1 Protease Cleavage Site Prediction

机译:特征选择与HIV-1蛋白酶切割位点预测的神经网络结构优化相结合

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摘要

It is crucial to understand the specificity of HIV-1 protease for designing HIV-1 protease inhibitors. In this paper, a new feature selection method combined with neural network structure optimization is proposed to analyze the specificity of HIV-1 protease and find the important positions in an octapeptide that determined its cleavability. Two kinds of newly proposed features based on Amino Acid Index database plus traditional orthogonal encoding features are used in this paper, taking both physiochemical and sequence information into consideration. Results of feature selection prove that p2, p1, p1', and p2' are the most important positions. Two feature fusion methods are used in this paper: combination fusion and decision fusion aiming to get comprehensive feature representation and improve prediction performance. Decision fusion of subsets that getting after feature selection obtains excellent prediction performance, which proves feature selection combined with decision fusion is an effective and useful method for the task of HIV-1 protease cleavage site prediction. The results and analysis in this paper can provide useful instruction and help designing HIV-1 protease inhibitor in the future.
机译:了解HIV-1蛋白酶用于设计HIV-1蛋白酶抑制剂的特异性至关重要。在本文中,提出了一种与神经网络结构优化结合的新特征选择方法,分析了HIV-1蛋白酶的特异性,并在八肽确定其可切割性的情况下找到重要的位置。本文使用了基于氨基酸指数数据库加上传统正交编码特征的两种新提出的特征,考虑了物理化学和序列信息。特征选择的结果证明了P2,P1,P1'和P2'是最重要的位置。本文使用了两个特征融合方法:组合融合和决策融合旨在获得全面的特征表示和提高预测性能。在特征选择之后获得的子集的决策融合获得了优异的预测性能,证明了特征选择与决策融合相结合,是HIV-1蛋白酶切割位点预测的任务的有效和有用的方法。本文的结果和分析可提供有用的指导和帮助在未来设计HIV-1蛋白酶抑制剂。

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