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In a nonrandom sample or a nonrandomized comparison of treated and control groups, methods are developed for displaying the sensitivity of confidence intervals for population quantiles to the magnitude of the departure from random selection. Quantiles of a single distribution and for a shift in two distributions are both discussed. These confidence intervals are based on a new inequality for the distribution of the number of successes in a nonrandom sample or nonrandomized comparison. The inequality has additional applications. In particular, it greatly accelerates the computations in a sensitivity analysis for the Mantel-Haenszel statistic in a 2 × 2 × S contingency table. Examples include a nonrandom collection of blood samples from a town with comparatively high levels of radon gas, an observational study of chromosome damage from mercury, and a study of the drug allopurinol as a cause of skin rash. The proof of the inequality makes use of Savage's lattice for ranks and Holley's inequality, which gives sufficient conditions for stochastic ordering in a lattice. [ABSTRACT FROM AUTHOR]

Some optimum nonparametric procedures for estimating and testing contrasts in two-way layouts are proposed and studied. These procedures are based on the Chernoff-Savage [4] type of rank order statistics which include the Wilcoxon and normal scores statistics among others. In the first three sections, the properties of the proposed point estimators of contrasts, such as symmetry, invariance and asymptotic normality, are studied and their asymptotic relative efficiencies with respect to the corresponding least-squares estimators are obtained. In particular, it is shown that the procedures based on the normal scores statistics are asymptotically at least as efficient as the corresponding procedures based on the method of least squares, whatever be parent cumulative distribution functions. In sections 4 and 5, the corresponding problems of testing and confidence intervals are discussed, and generalized to two-way layouts with several observations per cell. [ABSTRACT FROM AUTHOR]