Exact and approximate runs distributions

Let R = R_n denote the total (and unconditional) number of runs of successes or failures in a sequence of n Bernoulll (p) trials, where p is assumed to be known throughout. The exact distribution of R is related to a convolution of two negative binomial random variables with parameters p and q (=1-p). Using the representation of R as the sum of 1 - dependent indicators, a Berry - Esséen theorem is derived; the obtained rate of sup norm convergence is O(n^-½). This yields an unconditional version of the classical result of Wald and Wolfowitz (1940). The Stein - Chen method for m - dependent random variables is used, together with a suitable coupling, to prove a Poisson limit theorem for R. but with the limiting support set being the set of odd integers, Total variation error bounds (of order O(p) are found for the last result. Applications are indicated.     

Goodness of fit for the poisson distribution based on the probability generating function

For testing the fit of a discrete distribution, use of the probability generating function and its empirical counterpart has been suggested in Koeherlakota and Kocherlakota (1986). In the present paper, a particular functional of the corresponding empirical probability generating function process is proposed as a measure to test the discrepancy between the evidence and the hypothesis. The asymptotic behavior of the empirical probability generating function when a parameter is estimated is obtained, The study is exemplified for the Poisson case only but the procedure can be extended to other discrete distributions.     

Integral Representation of a Distribution Associated with a Pure Birth Process

ABSTRACT

This article deals with a distribution associated with a pure birth process starting with no individuals, with birth rates λ _n  = λ for n = 0, 2,…, m ? 1 and λ _n  = μ for n ≥ m. The probability mass function is expressed in terms of an integral that is very convenient for computing probabilities, moments, generating functions, and others. Using this representation, the kth factorial moments of the distribution is obtained. Some other forms of this distribution are also given.     

A Statistical Reanalysis of the Classical Rutherford's Experiment

Modified chi-squared and some newly developed tests for the Poisson, binomial, and an approximated Feller's distribution are discussed. A reanalysis of the classical Rutherford's experimental data on alpha decay is done. Previous analyses of the data were not correct from the point of view of the theory of statistical testing. Tests used show that the data contradict to both Poisson and binomial distribution and do not contradict to a precise “binomial” approximation of Feller's distribution that takes into account a counter's dead time. This gives a plausible statistically correct confirmation of the well-established exponential law of radioactive decay.     

信用贷款风险中反向CDS协议设计与定价模型

在信用违约互换(CDS协议)的基础上,提出了反向信用违约互换(RCDS)协议,以规避信用贷款风险.首先定义反向CDS协议,然后对反向CDS协议的定价合约进行设计,探讨反向CDS协议的风险“囚禁”原理;并在无套利的原则下,建立了含有未知违约概率的反向CDS协议定价模型;再进一步通过假设贷款企业的资产价值运动由一个布朗运动和若干个互相独立的泊松过程合成的复合泊松过程,在风险中性测度下,建立了资产价值运动的布朗运动和复合泊松过程随机微分方程,以此求出违约概率,并最终求出反向CDS协议定价公式.最后,通过数值分析,讨论了信用贷款利率、反向CDS价格、贷款期限、违约概率以及初始资产与违约边界之比等因素之间的相互影响关系,给出了相应风险规避方法的结论和建议.本文研究对实际应用具有很好的参考价值.     

Development of a novel machine learning-based weighted modeling approach to incorporate Salmonella enterica heterogeneity on a genetic scale in a dose–response modeling framework

Estimating microbial dose–response is an important aspect of a food safety risk assessment. In recent years, there has been considerable interest to advance these models with potential incorporation of gene expression data. The aim of this study was to develop a novel machine learning model that considers the weights of expression of Salmonella genes that could be associated with illness, given exposure, in hosts. Here, an elastic net-based weighted Poisson regression method was proposed to identify Salmonella enterica genes that could be significantly associated with the illness response, irrespective of serovar. The best-fit elastic net model was obtained by 10-fold cross-validation. The best-fit elastic net model identified 33 gene expression–dose interaction terms that added to the predictability of the model. Of these, nine genes associated with Salmonella metabolism and virulence were found to be significant by the best-fit Poisson regression model (p < 0.05). This method could improve or redefine dose–response relationships for illness from relative proportions of significant genes from a microbial genetic dataset, which would help in refining endpoint and risk estimations.     

A model-averaging treatment of multiple instruments in Poisson models with errors

We analyze Poisson regression when covariates contain measurement errors and when multiple potential instrumental variables are available. Without empirical knowledge to select the most suitable variable as an instrument, we propose a novel model-averaging approach to resolve this issue. We prescribe an implementation and establish its optimality in terms of minimizing prediction risk. We further show that, as long as one model is correctly specified among all potential instrumental variable models, our method will lead to consistent prediction. The performance of our method is illustrated through simulations and a movie sales example.     

Inventory Models with Continuous and Poisson Demands and Discounted and Average Costs

We develop a new, unified approach to treating continuous‐time stochastic inventory problems with both the average and discounted cost criteria. The approach involves the development of an adjusted discounted cycle cost formula, which has an appealing intuitive interpretation. We show for the first time that an (s, S) policy is optimal in the case of demand having a compound Poisson component as well as a constant rate component. Our demand structure simultaneously generalizes the classical EOQ model and the inventory models with Poisson demand, and we indicate the reasons why this task has been a difficult one. We do not require the surplus cost function to be convex or quasi‐convex as has been assumed in the literature. Finally, we show that the optimal s is unique, but we do not know if optimal S is unique.