Sample efficiencyof ESRL is independent of the chosen risk aversion threshold and quality of the behavior policy.

Neural Information Processing Systems http://nips.cc/

SLR, but an explicit connection between the two had not been made.

We develop a near-optimal testing procedure under the framework of Gaussian differential privacy for simple as well as one- and two-sided tests under monotone likelihood ratio conditions. Our mechanism is based on a private mean estimator with data-driven clamping bounds, whose population risk matches the private minimax rate up to logarithmic factors. Using this estimator, we construct private test statistics that achieve the same asymptotic relative efficiency as the non-private, most powerful tests while maintaining conservative type I error control. In addition to our theoretical results, our numerical experiments show that our private tests outperform competing DP methods and offer comparable power to the non-private most powerful tests, even at moderately small sample sizes and privacy loss budgets.

The majority of our hypothesis tests are based on differentially private versions of the $F$-statistic for the general linear model framework, which are uniformly most powerful unbiased in the non-private setting. We also present another test for testing mixtures, based on the differentially private nonparametric tests of Couch, Kazan, Shi, Bray, and Groce (CCS 2019), which is especially suited for the small dataset regime. We show that the differentially private $F$-statistic converges to the asymptotic distribution of its non-private counterpart.

We only observe their transformed versions $h(\mathbf{x_s^i})$ and $g(\mathbf{x_t^i})$, for some known function class $h(\cdot)$ and $g(\cdot)$. Our goal is to perform a statistical test checking if $P_{\rm source}$ = $P_{\rm target}$ while removing the distortions induced by the transformations. This problem is closely related to concepts underlying numerous domain adaptation algorithms, and in our case, is motivated by the need to combine clinical and imaging based biomarkers from multiple sites and/or batches, where this problem is fairly common and an impediment in the conduct of analyses with much larger sample sizes. We develop a framework that addresses this problem using ideas from hypothesis testing on the transformed measurements, where in the distortions need to be estimated {\it in tandem} with the testing. We derive a simple algorithm and study its convergence and consistency properties in detail, and we also provide lower-bound strategies based on recent work in continuous optimization. On a dataset of individuals at risk for neurological disease, our results are competitive with alternative procedures that are twice as expensive and in some cases operationally infeasible to implement.

Our objective is to infer the true hypothesis with low error, while minimizing the number of action sampled.