Abstract: In this paper we introduce a Bayesian analysis of a spherical distri bution applied to rock joint orientation data in presence or not of a vector of covariates, where the response variable is given by the angle from the mean and the covariates are the components of the normal upwards vector. Standard simulation MCMC (Markov Chain Monte Carlo) methods have been used to obtain the posterior summaries of interest obtained from Win Bugs software. Illustration of the proposed methodology are given using a simulated data set and a real rock spherical data set from a hydroelectrical site.
Abstract: Breast cancer is the second most common type of cancer in the world (World Cancer Report, 2014 a, b). The evolution of breast cancer treatment usually allows a longer life of patients as well in many cases a relapse of the disease. Usually medical researchers are interested to analyze data denoting the time until the occurrence of an event of interest such as the time of death by cancer in presence of right censored data and some covariates. In some situations, we could have two lifetimes associated to the same patient, as for example, the time free of the disease until recurrence and the total lifetime of the patient. In this case, it is important to assume a bivariate lifetime distribution which describes the possible dependence between the two observations. We consider as an application, different parametric bivariate lifetime distributions to analyze a breast cancer data set considering continuous or discrete data. Inferences of interest are obtained under a statistical Bayesian approach. We get the posterior summaries of interest using existing MCMC (Markov Chain Monte Carlo) methods. The main goal of the study, is to compare the bivariate continuous and discrete distributions that better describes the breast cancer lifetimes.
The normal distribution is the most popular model in applications to real data. We propose a new extension of this distribution, called the Kummer beta normal distribution, which presents greater flexibility to model scenarios involving skewed data. The new probability density function can be represented as a linear combination of exponentiated normal pdfs. We also propose analytical expressions for some mathematical quantities: Ordinary and incomplete moments, mean deviations and order statistics. The estimation of parameters is approached by the method of maximum likelihood and Bayesian analysis. Likelihood ratio statistics and formal goodnessof-fit tests are used to compare the proposed distribution with some of its sub-models and non-nested models. A real data set is used to illustrate the importance of the proposed model.
The generalized gamma model has been used in several applied areas such as engineering, economics and survival analysis. We provide an extension of this model called the transmuted generalized gamma distribution, which includes as special cases some lifetime distributions. The proposed density function can be represented as a mixture of generalized gamma densities. Some mathematical properties of the new model such as the moments, generating function, mean deviations and Bonferroni and Lorenz curves are provided. We estimate the model parameters using maximum likelihood. We prove that the proposed distribution can be a competitive model in lifetime applications by means of a real data set.
Abstract: In this paper, we propose a flexible cure rate survival model by as suming that the number of competing causes of the event of interest follows the negative binomial distribution and the time to event follows a generalized gamma distribution. We define the negative binomial-generalized gamma distribution, which can be used to model survival data. The new model in cludes as special cases some of the well-known cure rate models discussed in the literature. We consider a frequentist analysis and nonparametric boot strap for parameter estimation of a negative binomial-generalized gamma regression model with cure rate. Then, we derive the appropriate matri ces for assessing local influence on the parameter estimates under different perturbation schemes and present some ways to perform global influence analysis. Finally, we analyze a real data set from the medical area.