Urban morphology has long been recognized as a factor shaping human mobility, yet comparative and formal classifications of urban form across metropolitan areas remain limited. Building on theoretical principles of urban structure and advances in unsupervised learning, we systematically classified the built environment of nine U.S. metropolitan areas using structural indicators such as density, connectivity, and spatial configuration. The resulting morphological types were linked to mobility patterns through descriptive statistics, marginal effects estimation, and post hoc statistical testing. Here we show that distinct urban forms are systematically associated with different mobility behaviors, such as reticular morphologies being linked to significantly higher public transport use (marginal effect = 0.49) and reduced car dependence (-0.41), while organic forms are associated with increased car usage (0.44), and substantial declines in public transport (-0.47) and active mobility (-0.30). These effects are statistically robust (p < 1e-19), highlighting that the spatial configuration of urban areas plays a fundamental role in shaping transportation choices. Our findings extend previous work by offering a reproducible framework for classifying urban form and demonstrate the added value of morphological analysis in comparative urban research. These results suggest that urban form should be treated as a key variable in mobility planning and provide empirical support for incorporating spatial typologies into sustainable urban policy design.

Missing values in high-dimensional, mixed-type datasets pose significant challenges for data imputation, particularly under Missing Not At Random (MNAR) mechanisms. Existing methods struggle to integrate local and global data characteristics, limiting performance in MNAR and high-dimensional settings. We propose an innovative framework, RefiDiff, combining local machine learning predictions with a novel Mamba-based denoising network efficiently capturing long-range dependencies among features and samples with low computational complexity. RefiDiff bridges the predictive and generative paradigms of imputation, leveraging pre-refinement for initial warm-up imputations and post-refinement to polish results, enhancing stability and accuracy. By encoding mixed-type data into unified tokens, RefiDiff enables robust imputation without architectural or hyperparameter tuning. RefiDiff outperforms state-of-the-art (SOT A) methods across missing-value settings, demonstrating strong performance in MNAR settings and superior out-of-sample generalization. Extensive evaluations on nine real-world datasets demonstrate its robustness, scalability, and effectiveness in handling complex missingness patterns.

Theoretically exploring the advantages of neural networks might be one of the most challenging problems in the AI era. An adaptive feature program has recently been proposed to analyze the feature learning characteristic property of neural networks in a more abstract way. Motivated by the celebrated Le Cam equivalence, we advocate the over-parametrized sequence models to further simplify the analysis of the training dynamics of adaptive feature program and present several supporting evidences for the adaptive feature program. More precisely, after having introduced the feature error measure (FEM) to characterize the quality of the learned feature, we show that the FEM is decreasing during the training process of several concrete adaptive feature models including linear regression, single/multiple index models, etc. We believe that this hints at the potential successes of the adaptive feature program.

Collecting high-quality labeled data remains a challenge in data-driven research, especially when each label is costly and time-consuming to obtain. In response, many fields have embraced machine learning as a practical solution for predicting unobserved labels, such as annotating satellite imagery in remote sensing [46] and predicting protein structures in proteomics [24]. Prediction-powered inference [1] is a methodological framework showing how to perform valid statistical inference despite the inherent biases in such predicted labels. Active statistical inference [51] was recently introduced to further enhance inference by actively selecting which data points to label. The basic idea is to compute the model's uncertainty scores for all data points and prioritize collecting those labels for which the predictive model is most uncertain. When the uncertainty scores appropriately reflect the model's errors, Zrnic and Cand` es [51] show that active inference can significantly outperform prediction-powered inference (which can essentially be thought of as active inference with naive uniform sampling), meaning it results in more accurate estimates and narrower confidence intervals. However, when uncertainty scores are of poor quality, active inference can result in overly noisy estimates and large confidence intervals.

Machine learning and data processing techniques relying on covariance information are widespread as they identify meaningful patterns in unsupervised and unlabeled settings. As a prominent example, Principal Component Analysis (PCA) projects data points onto the eigenvectors of their covariance matrix, capturing the directions of maximum variance. This mapping, however, falls short in two directions: it fails to capture information in low-variance directions, relevant when, e.g., the data contains high-variance noise; and it provides unstable results in low-sample regimes, especially when covariance eigenvalues are close. CoVariance Neural Networks (VNNs), i.e., graph neural networks using the covariance matrix as a graph, show improved stability to estimation errors and learn more expressive functions in the covariance spectrum than PCA, but require training and operate in a labeled setup. To get the benefits of both worlds, we propose Covariance Scattering Transforms (CSTs), deep untrained networks that sequentially apply filters localized in the covariance spectrum to the input data and produce expressive hierarchical representations via nonlinearities. We define the filters as covariance wavelets that capture specific and detailed covariance spectral patterns. We improve CSTs' computational and memory efficiency via a pruning mechanism, and we prove that their error due to finite-sample covariance estimations is less sensitive to close covariance eigenvalues compared to PCA, improving their stability. Our experiments on age prediction from cortical thickness measurements on 4 datasets collecting patients with neurodegenerative diseases show that CSTs produce stable representations in low-data settings, as VNNs but without any training, and lead to comparable or better predictions w.r.t. more complex learning models.

Detecting chemical modifications on RNA molecules remains a key challenge in epitranscriptomics. Traditional reverse transcription-based sequencing methods introduce enzyme- and sequence-dependent biases and fragment RNA molecules, confounding the accurate mapping of modifications across the transcriptome. Nanopore direct RNA sequencing offers a powerful alternative by preserving native RNA molecules, enabling the detection of modifications at single-molecule resolution. However, current computational tools can identify only a limited subset of modification types within well-characterized sequence contexts for which ample training data exists. Here, we introduce a model-free computational method that reframes modification detection as an anomaly detection problem, requiring only canonical (unmodified) RNA reads without any other annotated data. For each nanopore read, our approach extracts robust, modification-sensitive features from the raw ionic current signal at a site using the signature transform, then computes an anomaly score by comparing the resulting feature vector to its nearest neighbors in an unmodified reference dataset. We convert anomaly scores into statistical p-values to enable anomaly detection at both individual read and site levels. Validation on densely-modified \textit{E. coli} rRNA demonstrates that our approach detects known sites harboring diverse modification types, without prior training on these modifications. We further applyied this framework to dengue virus (DENV) transcripts and mammalian mRNAs. For DENV sfRNA, it led to revealing a novel 2'-O-methylated site, which we validate orthogonally by qRT-PCR assays. These results demonstrate that our model-free approach operates robustly across different types of RNAs and datasets generated with different nanopore sequencing chemistries.

Thermocouples are in widespread use in industry, but they are particularly susceptible to calibration drift in harsh environments. Self-validating thermocouples aim to address this issue by using a miniature phase-change cell (fixed-point) in close proximity to the measurement junction (tip) of the thermocouple. The fixed point is a crucible containing an ingot of metal with a known melting temperature. When the process temperature being monitored passes through the melting temperature of the ingot, the thermocouple output exhibits a "plateau" during melting. Since the melting temperature of the ingot is known, the thermocouple can be recalibrated in situ. Identifying the melting plateau to determine the onset of melting is reasonably well established but requires manual intervention involving zooming in on the region around the actual melting temperature, a process which can depend on the shape of the melting plateau. For the first time, we present a novel machine learning approach to recognize and identify the characteristic shape of the melting plateau and once identified, to quantity the point at which melting begins, along with its associated uncertainty. This removes the need for human intervention in locating and characterizing the melting point. Results from test data provided by CCPI Europe show 100% accuracy of melting plateau detection. They also show a cross-validated R2 of 0.99 on predictions of calibration drift.

We present a variety of projection-based linear regression algorithms with a focus on modern machine-learning models and their algorithmic performance. We study the role of the relaxation parameter in generalized Kaczmarz algorithms and establish a priori regret bounds with explicit $λ$-dependence to quantify how much an algorithm's performance deviates from its optimal performance. A detailed analysis of relaxation parameter is also provided. Applications include: explicit regret bounds for the framework of Kaczmarz algorithm models, non-orthogonal Fourier expansions, and the use of regret estimates in modern machine learning models, including for noisy data, i.e., regret bounds for the noisy Kaczmarz algorithms. Motivated by machine-learning practice, our wider framework treats bounded operators (on infinite-dimensional Hilbert spaces), with updates realized as (block) Kaczmarz algorithms, leading to new and versatile results.

We study an online linear regression setting in which the observed feature vectors are corrupted by noise and the learner can pay to reduce the noise level. In practice, this may happen for several reasons: for example, because features can be measured more accurately using more expensive equipment, or because data providers can be incentivized to release less private features. Assuming feature vectors are drawn i.i.d. from a fixed but unknown distribution, we measure the learner's regret against the linear predictor minimizing a notion of loss that combines the prediction error and payment. When the mapping between payments and noise covariance is known, we prove that the rate $\sqrt{T}$ is optimal for regret if logarithmic factors are ignored. When the noise covariance is unknown, we show that the optimal regret rate becomes of order $T^{2/3}$ (ignoring log factors). Our analysis leverages matrix martingale concentration, showing that the empirical loss uniformly converges to the expected one for all payments and linear predictors.

We revisit the problem of generating synthetic data under differential privacy. To address the core limitations of marginal-based methods, we propose the Private Adaptive Generative Adversarial Network with Bayes Network Structure (PrAda-GAN), which integrates the strengths of both GAN-based and marginal-based approaches. Our method adopts a sequential generator architecture to capture complex dependencies among variables, while adaptively regularizing the learned structure to promote sparsity in the underlying Bayes network. Theoretically, we establish diminishing bounds on the parameter distance, variable selection error, and Wasserstein distance. Our analysis shows that leveraging dependency sparsity leads to significant improvements in convergence rates. Empirically, experiments on both synthetic and real-world datasets demonstrate that PrAda-GAN outperforms existing tabular data synthesis methods in terms of the privacy-utility trade-off.