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Stochastic kriging has been widely employed for simulation metamodeling to predict the response surface of a complex simulation model. However, its use is limited to cases where the design space is low-dimensional, because the number of design points required for stochastic kriging to produce accurate prediction, in general, grows exponentially in the dimension of the design space. The large sample size results in both a prohibitive sample cost for running the simulation model and a severe computational challenge due to the need of inverting large covariance matrices. Based on tensor Markov kernels and sparse grid experimental designs, we develop a novel methodology that dramatically alleviates the curse of dimensionality. We show that the sample complexity of the proposed methodology grows very mildly in the dimension, even under model misspecification. We also develop fast algorithms that compute stochastic kriging in its exact form without any approximation schemes. We demonstrate via extensive numerical experiments that our methodology can handle problems with a design space of more than 10,000 dimensions, improving both prediction accuracy and computational efficiency by orders of magnitude relative to typical alternative methods in practice.
Estimating copulas with discrete marginal distributions is challenging, especially in high dimensions, because computing the likelihood contribution of each observation requires evaluating $2^{J}$ terms, with $J$ the number of discrete variables. Cur
The vast availability of large scale, massive and big data has increased the computational cost of data analysis. One such case is the computational cost of the univariate filtering which typically involves fitting many univariate regression models a
This article proposes a visualization method for multidimensional data based on: (i) Animated functional Hypothetical Outcome Plots (f-HOPs); (ii) 3-dimensional Kiviat plot; and (iii) data sonification. In an Uncertainty Quantification (UQ) framework
Complex phenomena in engineering and the sciences are often modeled with computationally intensive feed-forward simulations for which a tractable analytic likelihood does not exist. In these cases, it is sometimes necessary to estimate an approximate
Simulation offers a simple and flexible way to estimate the power of a clinical trial when analytic formulae are not available. The computational burden of using simulation has, however, restricted its application to only the simplest of sample size