Admissible anytime-valid sequential inference must rely on nonnegative martingales
Aaditya Ramdas, Johannes Ruf, Martin Larsson, Wouter Koolen

TL;DR
This paper proves that for anytime-valid sequential inference, all admissible methods must fundamentally rely on nonnegative martingales, establishing their universality and optimality in this setting.
Contribution
The paper demonstrates that all admissible constructions of confidence sequences, p-processes, or e-processes in sequential inference must use nonnegative martingales, establishing their fundamental role.
Findings
Nonnegative martingales are necessary for admissible sequential inference methods.
The subGaussian supermartingale is shown to be admissible.
New constructions challenge previous methods in symmetry testing.
Abstract
Confidence sequences, anytime p-values (called p-processes in this paper), and e-processes all enable sequential inference for composite and nonparametric classes of distributions at arbitrary stopping times. Examining the literature, one finds that at the heart of all these (quite different) approaches has been the identification of nonnegative (super)martingales. Thus, informally, nonnegative (super)martingales are known to be sufficient for \emph{anytime-valid} sequential inference, even in composite and nonparametric settings. Our central contribution is to show that nonnegative martingales are also universal -- after appropriately defining \emph{admissibility}, we show that all admissible constructions of confidence sequences, p-processes, or e-processes must necessarily utilize nonnegative martingales. Our proofs utilize several modern mathematical tools for composite testing and…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsStatistical Methods and Inference · Statistical Methods in Clinical Trials · Advanced Statistical Process Monitoring
