Chase Mathis, Ian Waudby-Smithstat.ME math.ST stat.ML
Anytime-valid inference enables analysts to continuously monitor their data and stop experiments early. However, the majority of these methods incur a certain conservativeness by remaining valid on infinite time horizons. In practice, a bound on the horizon may be imposed due to budgetary, practical, or ethical constraints. In this paper, we ask the question: "Is it possible to obtain sharper large-sample anytime-valid inference by forgoing validity beyond some finite time horizon?". We provide a positive answer to this question by proposing a family of statistical objects that we call "confidence horizons". These objects can be viewed as large-sample confidence sequences on bounded time horizons, or alternatively as group sequential repeated confidence intervals with a maximal number of interim peeking times. We make explicit connections to the group sequential boundaries of Pocock [1977], O'Brien--Fleming [1979], and Wang--Tsiatis [1987]. We derive closed-form distribution functions of certain statistics which can be used to calculate the asymptotic quantiles of confidence horizons exactly, sidestepping the repeated integration typically employed in group sequential methods. We illustrate the use of confidence horizons for treatment effect estimation in sequentially randomized experiments under adaptive Neyman allocation.
Mechanistic interpretability often evaluates explanations by intervening on a model: swapping hidden states, patching activations, ablating components, or comparing a compressed model to the original one. These experiments are usually summarized by a point estimate, even though the evaluation may be monitored while it runs or adapted toward suspected failures. This makes it hard to tell whether a reported fidelity or patching effect is a stable causal claim or a consequence of finite sampling and evaluation choices. We introduce Certified Interventional Fidelity (CIF), a statistical layer for interventional interpretability evaluations. CIF first writes the quantity being reported as a causal estimand: an expectation of a bounded score over a stated input distribution and a stated intervention distribution. It then provides confidence intervals and anytime-valid confidence sequences for this estimand, including under adaptive intervention sampling via bounded mixture importance weighting. We instantiate CIF with Hoeffding-style sequences and variance-adaptive betting sequences, the latter reducing certification cost by 10-30x in our experiments. On MNIST abstractions and GPT-2 Small IOI circuits, CIF certifies high-fidelity claims, shows when apparent method differences are not statistically supported, and makes sensitivity to the intervention distribution explicit.
Yuan-chin Ivan Changcs.LG stat.AP stat.CO stat.ME stat.ML
Recurrent neural networks maintain a hidden state $h_t$, but its probabilistic meaning is often unclear. We study hidden-state stability through \emph{backward coherence}: the extent to which $h_t$ can be reconstructed from $h_{t+1}$ by a learned backward projector $g_φ$. Under contraction and summable backward drift, the hidden-state sequence forms a quasi-reverse-martingale. This yields almost-sure convergence, rates under mixing, an interpretable limiting representation, finite pathwise stopping times, and a theoretical framework for time-uniform confidence sequences. Simulations support the theory. Backward-coherence regularisation reduces the empirical quasi-martingale total $\hat Q$ by $43$--$58%$, reaches stability $28$--$44%$ earlier than an unregularised RNN, and gives tracking-error recovery consistent with geometric bounds. Additional tests confirm echo-state forgetting rates bounded by $ρ$ and verify the increment-sum tube $R_t$ with $100%$ simultaneous coverage, although $R_t$ is conservative; in practice, the defect-tail proxy $\hat Q_t$ is the more useful monitor. The backward-coherence loss is also equivalent to minimising a Kullback--Leibler divergence in a Gaussian backward model, linking the method to variational inference. Extensions cover $φ$-mixing inputs, change-point tracking, and finite-sample concentration. Three real-data studies further validate the approach. On PhysioNet 2012 ICU data, the Reverse Martingale RNN (RMRNN) matches RNN mortality-prediction AUC while reaching stable representations 13 hours earlier. On FRED-MD, it reduces one-month-ahead forecast error by about fourfold under concept drift. On UCI Human Activity Recognition, it maintains lower post-transition tracking error with geometric decay. The guarantees apply under the stated assumptions; universality is not claimed.