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Multiobjective evolutionary-based multi-kernel learner for realizing transfer learning in the prediction of HIV-1 protease cleavage sites

机译:基于多目标进化的多核学习者,用于实现HIV-1蛋白酶切割位点预测的转移学习

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摘要

Due to the unavailability of adequate patients and expensive labeling cost, many real-world biomedical cases have scarcity in the annotated data. This holds very true for HIV-1 protease specificity problem where only a few experimentally verified cleavage sites are present. The challenge then is to exploit the auxiliary data. However, the problem becomes more complicated when the underlying train and test data are generated from different distributions. To deal with the challenges, we formulate the HIV-1 protease cleavage site prediction problem into a bi-objective optimization problem and solving it by introducing a multiobjective evolutionary-based multi-kernel model. A solution for the optimization problem will lead us to decide the optimal number of base kernels with the best pairing of features. The bi-objective criteria encourage different individual kernels in the ensemble to mitigate the effect of distribution difference in training and test data with the ideal number of base kernels. In this paper, we considered eight different feature descriptors and three different kernel variants of support vector machines to generate the optimal multi-kernel learning model. Non-dominated sorting genetic algorithm-II is employed with bi-objective of achieving a maximum area under the receiver operating characteristic curve simultaneously with a minimum number of features. To validate the effectiveness of the model, the experiments were performed on four HIV-1 protease datasets. The performance comparison with fifteen state-of-the-art techniques on average accuracy and area under curve has been evaluated to justify the improvement of the proposed model. We then analyze Friedman and post hoc tests to demonstrate the significant improvement. The result obtained following the extensive experiment enumerates the bi-objective multi-kernel model performance enhancement on within and cross-learning over the other state-of-the-art techniques.
机译:由于足够患者的不可用和昂贵的标签成本,许多现实世界生物医学病例在注释数据中缺乏稀缺。对于HIV-1蛋白酶特异性问题,这对于仅存在少数实验验证的裂解位点来保持非常真实。然后挑战是利用辅助数据。但是,当底层列车和测试数据从不同的分布生成时,问题变得更加复杂。为应对挑战,我们将HIV-1蛋白酶切割位点预测问题分为双目标优化问题,并通过引入基于多目标进化的多核模型来解决方案。优化问题的解决方案将导致我们决定具有最佳配对功能的基础内核数。双目标标准鼓励集合中的不同单个核,以减轻培训和测试数据的分布差异与理想的基础内核的影响。在本文中,我们考虑了八种不同的特征描述符和三种不同的支持向量机器的内核变体,以产生最佳的多核学习模型。非主导的分类遗传算法-II与双目标用于在接收器下的最大面积与最小特征的同时在接收器操作特性曲线下实现。为了验证模型的有效性,在四个HIV-1蛋白酶数据集上进行实验。已经评估了与平均精度和曲线下面积的十五现有技术的性能比较,以证明提出建议模型的改进。然后,我们分析弗里德曼和后HOC测试以证明重大改善。在广泛的实验之后获得的结果枚举了对其他最先进的技术内的基于和交叉学习的双目标多核模型性能提升。

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