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D. A. S. Fraser 《The American statistician》2019,73(1):135-147
ABSTRACTThis article has two objectives. The first and narrower is to formalize the p-value function, which records all possible p-values, each corresponding to a value for whatever the scalar parameter of interest is for the problem at hand, and to show how this p-value function directly provides full inference information for any corresponding user or scientist. The p-value function provides familiar inference objects: significance levels, confidence intervals, critical values for fixed-level tests, and the power function at all values of the parameter of interest. It thus gives an immediate accurate and visual summary of inference information for the parameter of interest. We show that the p-value function of the key scalar interest parameter records the statistical position of the observed data relative to that parameter, and we then describe an accurate approximation to that p-value function which is readily constructed. 相似文献
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Adonis Yatchew 《统计学通讯:理论与方法》2013,42(6):1905-1926
The papsr considers distributions of collections of ratios of normal variables, The derivation of the joint density is linked to SKI sting literature on absolute, incomplete or truncated moments of multinormals. The distribution function may be expressed as a sum of rectangular multi normal probabilities. When the coefficients of variation of the denominators are close to zero, then a simple transformation of the ratios is approximately inultinormal. An application to Bayesian analysis is included. 相似文献
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In multiple comparisons of fixed effect parameters in linear mixed models, treatment effects can be reported as relative changes or ratios. Simultaneous confidence intervals for such ratios had been previously proposed based on Bonferroni adjustments or multivariate normal quantiles accounting for the correlation among the multiple contrasts. We propose Fieller-type intervals using multivariate t quantiles and the application of Markov chain Monte Carlo techniques to sample from the joint posterior distribution and construct percentile-based simultaneous intervals. The methods are compared in a simulation study including bioassay problems with random intercepts and slopes, repeated measurements designs, and multicenter clinical trials. 相似文献
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