Showing papers by "Pritam Ranjan published in 2020"
TL;DR: It is found that a large number of patents expire at an early stage leaving few patents with high value corroborating the results of studies using European, American and Chinese data.
Abstract: This study uses patent renewal information to estimate the private value of patents. Patent value refers to the economic reward that the inventor extracts from commercialising the patented inventio...
20 citations
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TL;DR: This work investigates a sequential approach of contour estimation via expected improvement criterion and proposes to use spline smoothing of the target response series to identify $k$ as the optimal number of knots, and the discretization time points as the actual location of the knots.
Abstract: In this paper we consider a dynamic computer simulator that produces a time-series response $y_t(x)$ over $L$ time points, for every given input parameter $x$. We propose a method for solving inverse problems, which refer to the finding of a set of inputs that generates a pre-specified simulator output. Inspired by the sequential approach of contour estimation via expected improvement criterion developed by Ranjan et al. (2008, DOI: 10.1198/004017008000000541), our proposed method discretizes the target response series on $k \; (\ll L)$ time points, and then iteratively solves $k$ scalar-valued inverse problems with respect to the discretized targets. We also propose to use spline smoothing of the target response series to identify the optimal number of knots, $k$, and the actual location of the knots for discretization. The performance of the proposed methods is compared for several test-function based computer simulators and the motivating real application that uses a rainfall-runoff measurement model named Matlab-Simulink model.
3 citations
TL;DR: This article proposes two new methods of design approaches that sequentially select input settings to achieve the goal of producing more accurate prediction which is important for risk assessment and decision making.
Abstract: Computer simulators are widely used to understand complex physical systems in many areas such as aerospace, renewable energy, climate modelling, and manufacturing. One fundamental aspect of the study of computer simulators is known as experimental design, that is, how to select the input settings where the computer simulator is run and the corresponding response is collected. Extra care should be taken in the selection process because computer simulators can be computationally expensive to run. The selection should acknowledge and achieve the goal of the analysis. This article focuses on the goal of producing more accurate prediction which is important for risk assessment and decision making. We propose two new methods of design approaches that sequentially select input settings to achieve this goal. The approaches make novel applications of simultaneous and sequential contour estimations. Numerical examples are employed to demonstrate the effectiveness of the proposed approaches.
2 citations
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TL;DR: IsoCheck as mentioned in this paper is a R library that checks the isomorphism of multi-stage 2^n factorial experiments with randomization restrictions, and recasts the problem of searching over all possible relabelings as a search over collineations, then exploits projective geometric properties of the space.
Abstract: Factorial designs are often used in various industrial and sociological experiments to identify significant factors and factor combinations that may affect the process response. In the statistics literature, several studies have investigated the analysis, construction, and isomorphism of factorial and fractional factorial designs. When there are multiple choices for a design, it is helpful to have an easy-to-use tool for identifying which are distinct, and which of those can be efficiently analyzed/has good theoretical properties. For this task, we present an R library called IsoCheck that checks the isomorphism of multi-stage 2^n factorial experiments with randomization restrictions. Through representing the factors and their combinations as a finite projective geometry, IsoCheck recasts the problem of searching over all possible relabelings as a search over collineations, then exploits projective geometric properties of the space to make the search much more efficient. Furthermore, a bitstring representation of the factorial effects is used to characterize all possible rearrangements of designs, thus facilitating quick comparisons after relabeling. We present several examples with R code to illustrate the usage of the main functions in IsoCheck. Besides checking equivalence and isomorphism of 2^n multi-stage factorial designs, we demonstrate how the functions of the package can be used to create a catalog of all non-isomorphic designs, and subsequently rank these designs based on a suitably defined ranking criterion. IsoCheck is free software and distributed under the General Public License and available from the Comprehensive R Archive Network.
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TL;DR: This chapter discusses the evolution of dynamic GP model - a computationally efficient statistical surrogate for a computer simulator with time series outputs and focuses on a recently discovered reliable vaccine called Mos-Quirix (RTS,S) which is currently going under human trials.
Abstract: Gaussian process (GP) based statistical surrogates are popular, inexpensive substitutes for emulating the outputs of expensive computer models that simulate real-world phenomena or complex systems. Here, we discuss the evolution of dynamic GP model - a computationally efficient statistical surrogate for a computer simulator with time series outputs. The main idea is to use a convolution of standard GP models, where the weights are guided by a singular value decomposition (SVD) of the response matrix over the time component. The dynamic GP model also adopts a localized modeling approach for building a statistical model for large datasets.
In this chapter, we use several popular test function based computer simulators to illustrate the evolution of dynamic GP models. We also use this model for predicting the coverage of Malaria vaccine worldwide. Malaria is still affecting more than eighty countries concentrated in the tropical belt. In 2019 alone, it was the cause of more than 435,000 deaths worldwide. The malice is easy to cure if diagnosed in time, but the common symptoms make it difficult. We focus on a recently discovered reliable vaccine called Mos-Quirix (RTS,S) which is currently going under human trials. With the help of publicly available data on dosages, efficacy, disease incidence and communicability of other vaccines obtained from the World Health Organisation, we predict vaccine coverage for 78 Malaria-prone countries.