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A new maximum entropy-based importance sampling for reliability analysis

机译:一种基于最大熵的重要度可靠性抽样新方法

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Importance sampling can be highly efficient if a good importance sampling density is constructed. Although the parametric sampling densities centered on the design points are often good choices, the determination of the design points can be a difficult and inefficient task itself, especially for problems with multiple design points, or highly nonlinear limit state functions. This paper introduces a nonparametric importance sampling method based on the Markov chain simulation and maximum-entropy density estimation (MEDE). In the proposed method, Markov chain simulation is utilized to generate samples that distribute asymptotically to the optimal importance sampling density. A nonparametric estimation of the optimal importance sampling density is then obtained using the MEDE technique. The conventional MEDE method is difficult for multi-dimensional problems as it needs to solve a set of simultaneous nonlinear integral equations. This paper developed a new MEDE technique for multivariate dataset. The method starts with using histogram to approximate a density. The multi-dimensional histogram is converted into a series of one-dimensional conditional PDFs in each dimension and the density is reconstructed by means of orthogonal expansion. Thus, the solution of MEDE is converted to a set of coefficients of the Legendre polynomials. The new importance sampling method is illustrated and compared with the classical kernel-based importance sampling using a number of numerical and structural examples. (C) 2016 Elsevier Ltd. All rights reserved.
机译:如果构建了重要的抽样密度,那么重要性抽样将非常高效。尽管以设计点为中心的参数采样密度通常是不错的选择,但确定设计点本身可能是一项困难且效率低的任务,尤其是对于具有多个设计点或高度非线性极限状态函数的问题。本文介绍了一种基于马尔可夫链模拟和最大熵密度估计(MEDE)的非参数重要性抽样方法。在提出的方法中,利用马尔可夫链模拟来生成样本,这些样本渐近地分布到最佳重要性采样密度。然后使用MEDE技术获得最佳重要性采样密度的非参数估计。传统的MEDE方法很难解决多维问题,因为它需要求解一组联立的非线性积分方程。本文为多元数据集开发了一种新的MEDE技术。该方法开始于使用直方图来近似密度。将多维直方图转换为每个维度中的一系列一维条件PDF,并通过正交展开重建密度。因此,将MEDE的解转换为Legendre多项式的一组系数。阐述了新的重要性采样方法,并使用许多数字和结构示例将其与基于经典内核的重要性采样进行了比较。 (C)2016 Elsevier Ltd.保留所有权利。

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