No Arabic abstract
The use of entropy related concepts goes from physics, such as in statistical mechanics, to evolutionary biology. The Shannon entropy is a measure used to quantify the amount of information in a system, and its estimation is usually made under the frequentist approach. In the present paper, we introduce an fully objective Bayesian analysis to obtain this measures posterior distribution. Notably, we consider the Gamma distribution, which describes many natural phenomena in physics, engineering, and biology. We reparametrize the model in terms of entropy, and different objective priors are derived, such as Jeffreys prior, reference prior, and matching priors. Since the obtained priors are improper, we prove that the obtained posterior distributions are proper and their respective posterior means are finite. An intensive simulation study is conducted to select the prior that returns better results in terms of bias, mean square error, and coverage probabilities. The proposed approach is illustrated in two datasets, where the first one is related to the Achaemenid dynasty reign period, and the second data describes the time to failure of an electronic component in the sugarcane harvest machine.
We study a nonparametric Bayesian approach to estimation of the volatility function of a stochastic differential equation driven by a gamma process. The volatility function is modelled a priori as piecewise constant, and we specify a gamma prior on its values. This leads to a straightforward procedure for posterior inference via an MCMC procedure. We give theoretical performance guarantees (contraction rates for the posterior) for the Bayesian estimate in terms of the regularity of the unknown volatility function. We illustrate the method on synthetic and real data examples.
In this paper we propose to make Bayesian inferences for the parameters of the Lomax distribution using non-informative priors, namely the Jeffreys prior and the reference prior. We assess Bayesian estimation through a Monte Carlo study with 500 simulated data sets. To evaluate the possible impact of prior specification on estimation, two criteria were considered: the bias and square root of the mean square error. The developed procedures are illustrated on a real data set.
For in vivo research experiments with small sample sizes and available historical data, we propose a sequential Bayesian method for the Behrens-Fisher problem. We consider it as a model choice question with two models in competition: one for which the two expectations are equal and one for which they are different. The choice between the two models is performed through a Bayesian analysis, based on a robust choice of combined objective and subjective priors, set on the parameters space and on the models space. Three steps are necessary to evaluate the posterior probability of each model using two historical datasets similar to the one of interest. Starting from the Jeffreys prior, a posterior using a first historical dataset is deduced and allows to calibrate the Normal-Gamma informative priors for the second historical dataset analysis, in addition to a uniform prior on the model space. From this second step, a new posterior on the parameter space and the models space can be used as the objective informative prior for the last Bayesian analysis. Bayesian and frequentist methods have been compared on simulated and real data. In accordance with FDA recommendations, control of type I and type II error rates has been evaluated. The proposed method controls them even if the historical experiments are not completely similar to the one of interest.
In many applications, the dataset under investigation exhibits heterogeneous regimes that are more appropriately modeled using piece-wise linear models for each of the data segments separated by change-points. Although there have been much work on change point linear regression for the low dimensional case, high-dimensional change point regression is severely underdeveloped. Motivated by the analysis of Minnesota House Price Index data, we propose a fully Bayesian framework for fitting changing linear regression models in high-dimensional settings. Using segment-specific shrinkage and diffusion priors, we deliver full posterior inference for the change points and simultaneously obtain posterior probabilities of variable selection in each segment via an efficient Gibbs sampler. Additionally, our method can detect an unknown number of change points and accommodate different variable selection constraints like grouping or partial selection. We substantiate the accuracy of our method using simulation experiments for a wide range of scenarios. We apply our approach for a macro-economic analysis of Minnesota house price index data. The results strongly favor the change point model over a homogeneous (no change point) high-dimensional regression model.
This paper is concerned with making Bayesian inference from data that are assumed to be drawn from a Bingham distribution. A barrier to the Bayesian approach is the parameter-dependent normalising constant of the Bingham distribution, which, even when it can be evaluated or accurately approximated, would have to be calculated at each iteration of an MCMC scheme, thereby greatly increasing the computational burden. We propose a method which enables exact (in Monte Carlo sense) Bayesian inference for the unknown parameters of the Bingham distribution by completely avoiding the need to evaluate this constant. We apply the method to simulated and real data, and illustrate that it is simpler to implement, faster, and performs better than an alternative algorithm that has recently been proposed in the literature.