...
首页> 外文期刊>Expert Systems with Application >Evolutionary based optimal ensemble classifiers for HIV-1 protease cleavage sites prediction
【24h】

Evolutionary based optimal ensemble classifiers for HIV-1 protease cleavage sites prediction

机译:基于进化的HIV-1蛋白酶切割位点预测的最佳集成分类器

获取原文
获取原文并翻译 | 示例
           

摘要

HIV-1 protease site helps to understand the specificity of substrates which antagonizes AIDS by restraining the replication of HIV-1 through inhibitors. Identification of HIV-1 protease cleavage sites by experimental methods are usually labor-intensive thus time-consuming. Several computational intelligence methods have been evaluated to predict cleavage sites. However, due to inconsistent findings regarding the superiority of one classifier over another and the usefulness of encoding techniques in general, more research is needed to provide advance confidence in computational results. The success of an HIV cleavage site prediction system depends heavily on two things: the classifier being used and the features encoding technique applied. For the cleavage sites identification, the role of appropriate feature encoding has not been paid adequate importance. In this investigation, we use two novel ideas for HIV Cleavage site prediction. First, we propose an optimal ensemble formation technique that optimizes the search space of 2(28) formed by seven encoding techniques and four SVM kernels (7 x 4) with the use of genetic algorithm. The second is the utilization of area under receiver operating characteristics (AUC) as a fitness measure for the evaluation of optimal ensemble. The evolutionary algorithm is encoded with binary strings to decide the correlation between the encoding-classifier pair in an ensemble. The proposed method with new ensembling encoding-classifier pair increases the HIV cleavage site prediction significantly. Overall, an appealing degree of predictive accuracy is observed by evolutionary-based ensemble model and hence becomes a valid and best alternative for peptide classification. (C) 2018 Elsevier Ltd. All rights reserved.
机译:HIV-1蛋白酶位点通过抑制抑制剂抑制HIV-1的复制,有助于了解拮抗AIDS的底物的特异性。通过实验方法鉴定HIV-1蛋白酶切割位点通常是费力的,因此很费时。已经评估了几种计算智能方法来预测切割位点。但是,由于关于一个分类器优于另一个分类器的优缺点以及总体上编码技术的有用性的不一致发现,需要进行更多的研究以提供对计算结果的增强信心。 HIV裂解位点预测系统的成功在很大程度上取决于两件事:使用的分类器和应用的特征编码技术。对于切割位点的鉴定,适当特征编码的作用尚未得到足够重视。在这项调查中,我们使用两个新颖的想法进行HIV卵裂位点预测。首先,我们提出了一种最佳的集合形成技术,该算法使用遗传算法优化了由7种编码技术和4个SVM内核(7 x 4)形成的2(28)的搜索空间。第二个方面是利用接收器工作特性(AUC)下的面积作为适合度评估最佳集成度。用二进制字符串对进化算法进行编码,以决定整体中的编码分类器对之间的相关性。带有新的集成编码分类器对的拟议方法显着提高了HIV切割位点的预测。总体而言,基于进化的集成模型可观察到令人满意的预测准确度,因此成为肽类分类的有效且最佳选择。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号