This gives rise to the RTK-MALA and RTK-ULD algorithms for diffusion inference.

It is well known that this is unlearnable, but we sketch a proof here.

The implementations of the experiments on ABC and FTDC datasets are similar. For the stability analysis, we are interested in the norm of term 1. In Section E.1, we briefly discuss the motivation behind studying age prediction and PCA-based statistical analysis in this context. In Section E.2, we provide additional details on cortical thickness data acquisition. In Section E.3, we report the results for stability analysis of VNNs and PCA-regression models for FTDC100 ( In Section E.4, we study the stability of VNNs on two simulated In Section E.5, we include additional figures A promising application of brain age prediction is early detection of neurodegenerative diseases (such as Alzheimer's, Huntingson's disease) which may manifest themselves as error in age prediction in pathological contexts by machine learning models trained E.4 Stability of VNNs on Synthetic Data We consider two settings for synthetic data.

It is well known that this is unlearnable, but we sketch a proof here.

We study masked discrete diffusion -- a flexible paradigm for text generation in which tokens are progressively corrupted by special mask symbols before being denoised. Although this approach has demonstrated strong empirical performance, its theoretical complexity in high-dimensional settings remains insufficiently understood. Existing analyses largely focus on uniform discrete diffusion, and more recent attempts addressing masked diffusion either (1) overlook widely used Euler samplers, (2) impose restrictive bounded-score assumptions, or (3) fail to showcase the advantages of masked discrete diffusion over its uniform counterpart. To address this gap, we show that Euler samplers can achieve $ε$-accuracy in total variation (TV) with $\tilde{O}(d^{2}ε^{-3/2})$ discrete score evaluations, thereby providing the first rigorous analysis of typical Euler sampler in masked discrete diffusion. We then propose a Mask-Aware Truncated Uniformization (MATU) approach that both removes bounded-score assumptions and preserves unbiased discrete score approximation. By exploiting the property that each token can be unmasked at most once, MATU attains a nearly $ε$-free complexity of $O(d\,\ln d\cdot (1-ε^2))$. This result surpasses existing uniformization methods under uniform discrete diffusion, eliminating the $\ln(1/ε)$ factor and substantially speeding up convergence. Our findings not only provide a rigorous theoretical foundation for masked discrete diffusion, showcasing its practical advantages over uniform diffusion for text generation, but also pave the way for future efforts to analyze diffusion-based language models developed under masking paradigm.

The implementations of the experiments on ABC and FTDC datasets are similar. For the stability analysis, we are interested in the norm of term 1. In Section E.1, we briefly discuss the motivation behind studying age prediction and PCA-based statistical analysis in this context. In Section E.2, we provide additional details on cortical thickness data acquisition. In Section E.3, we report the results for stability analysis of VNNs and PCA-regression models for FTDC100 ( In Section E.4, we study the stability of VNNs on two simulated In Section E.5, we include additional figures A promising application of brain age prediction is early detection of neurodegenerative diseases (such as Alzheimer's, Huntingson's disease) which may manifest themselves as error in age prediction in pathological contexts by machine learning models trained E.4 Stability of VNNs on Synthetic Data We consider two settings for synthetic data.

Continuous diffusion models have demonstrated remarkable performance in data generation across various domains, yet their efficiency remains constrained by two critical limitations: (1) the local adjacency structure of the forward Markov process, which restricts long-range transitions in the data space, and (2) inherent biases introduced during the simulation of time-inhomogeneous reverse denoising processes. To address these challenges, we propose Quantized Transition Diffusion (QTD), a novel approach that integrates data quantization with discrete diffusion dynamics. Our method first transforms the continuous data distribution $p_*$ into a discrete one $q_*$ via histogram approximation and binary encoding, enabling efficient representation in a structured discrete latent space. We then design a continuous-time Markov chain (CTMC) with Hamming distance-based transitions as the forward process, which inherently supports long-range movements in the original data space. For reverse-time sampling, we introduce a \textit{truncated uniformization} technique to simulate the reverse CTMC, which can provably provide unbiased generation from $q_*$ under minimal score assumptions. Through a novel KL dynamic analysis of the reverse CTMC, we prove that QTD can generate samples with $O(d\ln^2(d/ε))$ score evaluations in expectation to approximate the $d$--dimensional target distribution $p_*$ within an $ε$ error tolerance. Our method not only establishes state-of-the-art inference efficiency but also advances the theoretical foundations of diffusion-based generative modeling by unifying discrete and continuous diffusion paradigms.

Estimating treatment effects from observational data is challenging due to two main reasons: (a) hidden confounding, and (b) covariate mismatch (control and treatment groups not having identical distributions). Long lines of works exist that address only either of these issues. To address the former, conventional techniques that require detailed knowledge in the form of causal graphs have been proposed. For the latter, covariate matching and importance weighting methods have been used. Recently, there has been progress in combining testable independencies with partial side information for tackling hidden confounding. A common framework to address both hidden confounding and selection bias is missing. We propose neural architectures that aim to learn a representation of pre-treatment covariates that is a valid adjustment and also satisfies covariate matching constraints. We combine two different neural architectures: one based on gradient matching across domains created by subsampling a suitable anchor variable that assumes causal side information, followed by the other, a covariate matching transformation. We prove that approximately invariant representations yield approximate valid adjustment sets which would enable an interval around the true causal effect. In contrast to usual sensitivity analysis, where an unknown nuisance parameter is varied, we have a testable approximation yielding a bound on the effect estimate. We also outperform various baselines with respect to ATE and PEHE errors on causal benchmarks that include IHDP, Jobs, Cattaneo, and an image-based Crowd Management dataset.