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  • Open Access Icon
  • Research Article
  • 10.1093/biomet/asag031
Nonparametric Inference for Balance in Signed Networks
  • Apr 28, 2026
  • Biometrika
  • Xuyang Chen + 2 more

SUMMARY In many real-world networks, relationships often go beyond simple dyadic presence or absence; they can be positive, like friendship, alliance, and mutualism, or negative, characterized by enmity, disputes, and competition. To understand the formation mechanism of such signed networks, the social balance theory sheds light on the dynamics of positive and negative connections. In particular, it characterizes the proverbs, “a friend of my friend is my friend” and “an enemy of my enemy is my friend”. In this work, we propose a nonparametric inference approach for assessing empirical evidence for the balance theory in real-world signed networks. We first characterize the generating process of signed networks with node exchangeability and propose a nonparametric sparse signed graphon model. Under this model, we construct confidence intervals for the population parameters associated with balance theory and establish their theoretical validity. Our inference procedure is as computationally efficient as a simple normal approximation but offers higher-order accuracy. By applying our method, we find strong real-world evidence for balance theory in signed networks across various domains, extending its applicability beyond social psychology.

  • Research Article
  • 10.1093/biomet/asag019
Conditioning on posterior samples for flexible frequentist goodness-of-fit testing
  • Mar 28, 2026
  • Biometrika
  • Ritwik Bhaduri + 3 more

Summary Tests of goodness of fit are used in nearly every domain where statistics is applied.One powerful and flexible approach is to sample artificial data sets that are exchangeable with the real data under the null hypothesis (but not under the alternative), as this allows the analyst to conduct a valid test using any test statistic they desire. Such sampling is typically done by conditioning on either an exact or approximate sufficient statistic, but existing methods for doing so have significant limitations, which either preclude their use or substantially reduce their power or computational tractability for many important models. In this paper, we propose to condition on samples from a Bayesian posterior distribution, which constitute a very different type of approximate sufficient statistic than those considered in prior work. Our approach, approximately co-sufficient sampling via Bayes , considerably expands the scope of this flexible type of goodness-of-fit testing. We prove the approximate validity of the resulting test, and demonstrate its utility on three common null models where no existing methods apply, as well as its outperformance on models where existing methods do apply.

  • Research Article
  • 10.1093/biomet/asag017
Comparing causal parameters with many treatments and positivity violations
  • Mar 13, 2026
  • Biometrika
  • A Mcclean + 5 more

Summary Comparing outcomes across treatments is essential in medicine and public policy. To do so, researchers typically estimate a set of parameters, possibly counterfactual, each targeting a different treatment. Treatment-specific means are commonly used, but their identification requires a positivity assumption: every subject has a nonzero probability of receiving each treatment. This assumption is often implausible, especially when treatment can take many values. Causal parameters based on dynamic stochastic interventions offer robustness to positivity violations. However, comparing these parameters may fail to reflect the effects of the underlying target treatments because the parameters can depend on outcomes under nontarget treatments. To clarify when two parameters targeting different treatments yield a useful comparison of treatment efficacy, we propose a comparability criterion: if the conditional treatment-specific mean for one treatment is greater than that for another, then the corresponding causal parameter should also be greater. Many standard parameters fail to satisfy this criterion, but we show that only a mild positivity assumption is needed to identify parameters that yield useful comparisons. We then provide two simple examples that satisfy this criterion and are identifiable under the milder positivity assumption: trimmed and smooth-trimmed treatment-specific means with multivalued treatments. For smooth-trimmed treatment-specific means, we develop doubly robust-style estimators that attain parametric convergence rates under nonparametric conditions. We illustrate our methods with an analysis of dialysis providers in New York State.

  • Open Access Icon
  • Research Article
  • Cite Count Icon 2
  • 10.1093/biomet/asag012
Parameterising the effect of a continuous treatment using average derivative effects
  • Feb 19, 2026
  • Biometrika
  • Oliver J Hines + 2 more

Abstract The average treatment effect (ATE) is commonly used to quantify the main effect of a binary treatment on an outcome. Extensions to continuous treatments are usually based on the dose response curve or shift interventions, but both require strong overlap conditions and the resulting curves may be difficult to summarise. We focus instead on average derivative effects (ADEs) that are scalar estimands related to infinitesimal shift interventions requiring only local overlap assumptions. ADEs, however, are rarely used in practice because their estimation usually requires estimating conditional density functions. By characterising the Riesz representers of weighted ADEs,weproposeanewclassofestimandsthat provides a unified view of weighted ADEs/ATEs when the treatment is continuous/binary. We derive the estimand in our class that minimises the nonparametric efficiency bound, thereby extending optimal weighting results from the binary treatment literature to the continuous setting. We develop efficient estimators for two weighted ADEs that avoid density estimation and are amenable to modern machine learning methods, which we evaluate in simulations and an applied analysis of Warfarin dosage effects.

  • Research Article
  • 10.1093/biomet/asag013
Design-based Causal Inference for Incomplete Block Designs
  • Feb 19, 2026
  • Biometrika
  • Taehyeon Koo + 1 more

Abstract Researchers often turn to block randomization to increase the precision of their inference or due to practical considerations, such as in multisite trials. However, if the number of treatments under consideration is large it might not be feasible or practical to assign all treatments within each block. We develop novel inference results under the finite-population design-based framework for natural alternatives to the complete block design that do not require reducing the number of treatment arms, the incomplete block design and the balanced incomplete block design. This includes deriving the properties of two design-based estimators, developing a finite-population central limit theorem, and proposing conservative variance estimators.Comparisons of the design-based estimators are made to linear model-based estimators. Simulations and a data illustration further demonstrate performance of incomplete block design estimators. This work highlights incomplete block designs as practical and currently underutilized designs.

  • Research Article
  • 10.1093/biomet/asag010
Randomization-Based Confidence Sets for the Local Average Treatment Effect
  • Feb 16, 2026
  • Biometrika
  • P M Aronow + 2 more

Summary We consider the problem of generating confidence sets in randomized experiments with noncompliance. We show that a refinement of a randomization-based procedure proposed by Imbens & Rosenbaum (2005) has desirable properties. Specifically, we show that using a studentized Anderson–Rubin statistic as a test statistic yields confidence sets that are finite-sample exact under treatment effect homogeneity and remain asymptotically valid for the local average treatment effect when the treatment effects are heterogeneous. We provide a uniform analysis of this procedure and efficient algorithms to construct the confidence sets.

  • Open Access Icon
  • Research Article
  • Cite Count Icon 1
  • 10.1093/biomet/asag009
Estimating Ratios of Means of Multicategory Data Observed with Sample and Category Perturbations
  • Feb 13, 2026
  • Biometrika
  • D S Clausen + 2 more

Summay We consider the problem of estimating ratios of means of a multivariate outcome across covariates when the data are observed with unknown sample-specific and category-specific perturbations. Our model admits a partially identifiable estimand, and we establish full identifiability by imposing interpretable parameter constraints. To reduce bias and guarantee the existence of estimators in the presence of sparse observations, we apply an asymptotically negligible and constraint-invariant penalty to the loss function. We develop a fast coordinate-descent algorithm for estimation, and an augmented Lagrangian algorithm for estimation under null hypotheses. We construct a model-robust score test and demonstrate valid inference even for small sample sizes and under violated distributional assumptions. The flexibility of the approach, and comparisons with related methods, are illustrated through a simulation study and a meta-analysis of microbial associations with colorectal cancer.

  • Open Access Icon
  • Research Article
  • Cite Count Icon 1
  • 10.1093/biomet/asag007
Asymptotics for a class of parametric martingale posteriors
  • Feb 13, 2026
  • Biometrika
  • E Fong + 1 more

Summary The martingale posterior framework replaces the elicitation of the likelihood and prior with that of a sequence of one-step-ahead predictive densities for Bayesian inference. Posterior sampling then involves the imputation of unobserved quantities and can then be carried out in an expedient and parallelizable manner using predictive resampling, without requiring Markov chain Monte Carlo. Recent work has investigated the use of plug-in parametric predictive densities, combined with stochastic gradient descent, to specify a parametric martingale posterior. This paper investigates the asymptotic properties of this class of parametric martingale posteriors. In particular, two central limit theorems based on martingale limit theory are introduced and applied. The first is a predictive central limit theorem, which enables a significant acceleration of the predictive resampling scheme through a hybrid sampling algorithm based on a normal approximation. The second is a Bernstein–von Mises result, which is novel for martingale posteriors, and provides methodological guidance on attaining desirable frequentist properties. We demonstrate the utility of the theoretical results through simulations and a real data example.

  • Research Article
  • 10.1093/biomet/asag011
Inferring manifolds using Gaussian processes
  • Feb 13, 2026
  • Biometrika
  • David B Dunson + 1 more

Abstract It is often of interest to infer lower-dimensional structure underlying complex data. As a flexible class of nonlinear structures, it is common to focus on Riemannian manifolds. Most existing manifold-learning algorithms replace the original data with lower-dimensional coordinates without providing an estimate of the manifold or using it to denoise the original data. This article proposes a new methodology to address these issues, allowing interpolation of the estimated manifold between the fitted data points. The proposed approach is motivated by the novel theoretical properties of local covariance matrices constructed from samples near a manifold. Our results enable the transformation of a global manifold-reconstruction problem into a local regression problem, allowing the application of Gaussian processes for probabilistic manifold reconstruction. In addition to the theory justifying our methodology, we provide simulated and real data examples to illustrate its performance.

  • Research Article
  • 10.1093/biomet/asag008
Treatment choice with nonlinear regret
  • Feb 4, 2026
  • Biometrika
  • Toru Kitagawa + 2 more

Summary Following Savage (1951)and Manski (2004), the literature on statistical treatment choice focuses on the mean of welfare regret. Ignoring other features of the regret distribution, however, can lead to a rule that is sensitive to sampling uncertainty. We propose to minimize the mean of a nonlinear transformation of regret and show that singleton rules are not essentially complete for nonlinear regret. Focusing on mean-square regret, we derive closed-form fractions for finite-sample Bayes and minimax optimal rules. Our approach is grounded in decision theory and extends to limit experiments. The treatment fractions can be viewed as the strength of evidence favouring treatment. We apply our framework to a normal regression model and sample-size calculations.