Abstract:Tabular-to-image methods that convert tabular data into visual representations have emerged as a novel paradigm for leveraging the high performance of deep learning models. Despite their advantages, the robustness of these methods under distribution shifts remains under explored. Test-Time Augmentation (TTA) is an effective approach in image classification to improve model generalization and robustness, where predictions over multiple transformed views of each input are aggregated. This work evaluates the impact of TTA techniques on predictive performance under Out-Of-Distribution (OOD) for representations generated by tabular-to-image methods. Six tabular-to-image encoding methods were considered: TINTO, IGTD, DeepInsight, BIE, DistanceMatrix, Fotomics. Twenty-five TTA techniques were used, organized into six types: Geometric, Photometric, Structural, Frequency/Encoding, Mixup, and Composite. We employed two datasets from the TableShift benchmark (HELOC and Voting) that provide in-distribution and OOD test subsets designed to evaluate the effect of distribution shifts on tabular data. The results indicate that TTA improves OOD performance, with composite and photometric strategies providing the best trade-off between robustness and variance. In contrast, frequency-domain transformations that alter the encoder's feature-to-intensity mapping consistently degrade performance. These findings highlight TTA as a promising approach for improving the robustness and generalization of classifiers trained on image representations derived from tabular data, particularly under distribution shifts.
Abstract:Tabular Foundation Models (TFMs) have emerged as novel approaches for tabular predictive tasks, demonstrating competitive predictive performance to ensemble tree-based models. Most TFMs are trained and evaluated on independent and identically distributed data, but this assumption changes in real-world scenarios due to distribution shifts, which compromise the robustness of models. Limited research has been conducted of TFMs under distribution shifts. We present an empirical evaluation of Out-Of-Distribution (OOD) performance of nine TFMs, spanning diverse pre-training strategies and architectures: TabPFNv2, TabPFNv2.5, TabPFNv2.6, TabPFNv3, TabICL, TabICLv2, Mitra, LimiX and TabFM. Three real-world datasets from the TableShift study were considered (HELOC, Voting, Childhood Lead), covering label, socioeconomic, and geographic shift types. Our results show that all evaluated TFMs degrade systematically under distribution shift regardless of pre-training strategy, with shift gaps ranging from 0.003 to 0.060 depending on shift type. The relationship between in-distribution and OOD predictive performance documented for classical tabular models extends into TFMs. We also identified a scalability gap, as high-performing models demand significant memory and computational resources beyond what standard deployment infrastructure can support. This study extends existing benchmarks for OOD in tabular data, providing evidence to support their adoption in high-stakes domains characterized by structural distribution shifts.
Abstract:The IEC 61850 Generic Object-Oriented Substation Event (GOOSE) protocol plays a critical role in real-time protection and automation of digital substations, yet its lack of native security mechanisms can expose power systems to sophisticated cyberattacks. Traditional rule-based and supervised intrusion detection techniques struggle to detect protocol-compliant and zero-day attacks under significant class imbalance and limited availability of labeled data. This paper proposes an explainable, unsupervised multi-view anomaly detection framework for IEC 61850 GOOSE networks that explicitly separates semantic integrity and temporal availability. The approach employs asymmetric autoencoders trained only on real operational GOOSE traffic to learn distinct latent representations of sequence-based protocol semantics and timing-related transmission dynamics in normal traffic. Anomaly detection is implemented using reconstruction errors mixed with statistically grounded thresholds, enabling robust detection without specified attack types. Feature-level reconstruction analysis provides intrinsic explainability by directly linking detection outcomes to IEC 61850 protocol characteristics. The proposed framework is evaluated using real substation traffic for training and a public dataset containing normal traffic and message suppression, data manipulation, and denial-of-service attacks for testing. Experimental results show attack detection rates above 99% with false positives remaining below 5% of total traffic, demonstrating strong generalization across environments and effective operation under extreme class imbalance and interpretable anomaly attribution.
Abstract:This study explores a data-driven approach to discovering novel clinical and genetic markers in ovarian cancer (OC). Two main analyses were performed: (1) a nonlinear examination of an OC dataset using autoencoders, which compress data into a 3-dimensional latent space to detect potential intrinsic separability between platinum-sensitive and platinum-resistant groups; and (2) an adaptation of the informative variable identifier (IVI) to determine which features (clinical or genetic) are most relevant to disease progression. In the autoencoder analysis, a clearer pattern emerged when using clinical features and the combination of clinical and genetic data, indicating that disease progression groups can be distinguished more effectively after supervised fine tuning. For genetic data alone, this separability was less apparent but became more pronounced with a supervised approach. Using the IVI-based feature selection, key clinical variables (such as type of surgery and neoadjuvant chemotherapy) and certain gene mutations showed strong relevance, along with low-risk genetic factors. These findings highlight the strength of combining machine learning tools (autoencoders) with feature selection methods (IVI) to gain insights into ovarian cancer progression. They also underscore the potential for identifying new biomarkers that integrate clinical and genomic indicators, ultimately contributing to improved patient stratification and personalized treatment strategies.