Group testing is a technique employed in large screening studies involving infectious disease, where individuals in the study are grouped before being observed. Parametric and nonparametric estimators of conditional prevalence have been developed in the group testing literature, in the case where the binary variable indicating the disease status is available only for the group, but the explanatory variable is observed for each individual. However, for reasons such as the high cost of assays, the confidentiality of the patients, or the impossibility of measuring a concentration under a detection limit, the explanatory variable is observable only in an aggregated form and the existing techniques are no longer valid. We develop consistent parametric and nonparametric estimators of the conditional prevalence in this complex problem. We establish theoretical properties of our estimators and illustrate their practical performance on simulated and real data. We extend our techniques to the case where the group status is measured imperfectly, and to the setting where the covariate is aggregated and the individual status is available. Supplementary materials for this article are available online.

We consider nonparametric estimation of a regression curve when the data are observed with multiplicative distortion which depends on an observed confounding variable. We suggest several estimators, ranging from a relatively simple one that relies on restrictive assumptions usually made in the literature, to a sophisticated piecewise approach that involves reconstructing a smooth curve from an estimator of a constant multiple of its absolute value, and which can be applied in much more general scenarios. We show that, although our nonparametric estimators are constructed from predictors of the unobserved undistorted data, they have the same first-order asymptotic properties as the standard estimators that could be computed if the undistorted data were available. We illustrate the good numerical performance of our methods on both simulated and real datasets.