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Adaptive configuring of radial basis function network by hybrid particle swarm algorithm for QSAR studies of organic compounds

机译:基于混合粒子群算法的径向基函数网络自适应配置用于有机物的QSAR研究。

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The configuring of a radial basis function network (RBFN) consists of selecting the network parameters (centers and widths in RBF units and weights between the hidden and output layers) and network architecture. The issues of suboptimum and overfitting, however, often occur in RBFN configuring. This paper presented a hybrid particle swarm optimization (HPSO) algorithm to simultaneously search the optimal network structure and parameters involved in the RBFN (HPSORBFN) with an ellipsoidal Gaussian function as a basis function. The continuous version of PSO was used for parameter training, while the modified discrete PSO was employed to determine the appropriate network topology. The proposed HPSORBFN algorithm was applied to modeling the inhibitory activities of substituted bis[(acridine-4-carboxamide)propyl]methylamines to murine P388 leukemia cells and the bioactivities of COX-2 inhibitors. The results were compared with those obtained from RBFNs with the parameters optimized by continuous PSO and by conventionally RBFN training the algorithm for a fixed network topology, indicating that the HPSO was competent for RBFN configuring in that it converged quickly toward the optimal solution and avoided overfitting.
机译:径向基函数网络(RBFN)的配置包括选择网络参数(RBF单位的中心和宽度以及隐藏层和输出层之间的权重)和网络体系结构。然而,在RBFN配置中经常会出现次优和过度拟合的问题。本文提出了一种混合粒子群优化(HPSO)算法,以椭圆高斯函数为基础函数,同时搜索RBFN(HPSORBFN)涉及的最优网络结构和参数。 PSO的连续版本用于参数训练,而修改后的离散PSO用于确定适当的网络拓扑。提出的HPSORBFN算法被用于模拟取代的双[(ac啶-4-羧酰胺)丙基]甲胺对小鼠P388白血病细胞的抑制活性和COX-2抑制剂的生物活性。将结果与通过连续PSO和常规RBFN训练的固定网络拓扑算法优化的参数从RBFN获得的结果进行比较,表明HPSO能够胜任RBFN配置,因为它可以快速收敛到最佳解决方案并避免过度拟合。

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