Cybercrime has emerged as one of the most pervasive and economically destructive consequences of global digitalization. Contemporary online fraud and deception-based crimes now account for unprecedented financial losses worldwide, exceeding trillions of United States dollars (USD) annually (Morgan, 2016), while also inflicting severe psychological, social, and reputational harm on victims. Unlike classical cyberattacks targeting systems and networks, modern cybercrime increasingly exploits human vulnerabilities rather than purely technical weaknesses, relying on deception, persuasion, impersonation, emotional coercion, and trust manipulation as primary attack vectors (Holt, 2019; Yao, Zheng, Wu, Wu, Gao, Wang and Yang, 2025; Sarkar and Shukla, 2023; Sarkar, Singh, Kumar and Shukla, 2023). Existing cybersecurity frameworks, such as the Cyber Kill Chain and the MITRE ATT&CK framework, provide powerful abstractions for understanding technically sophisticated cyberattacks targeting enterprise systems and critical infrastructure (MITRE Corporation, 2025b,a). However, these models are fundamentally system-centric: they describe how adversaries compromise digital infrastructure, escalate privileges, and exfiltrate data. In contrast, cybercrime, particularly scams, fraud, impersonation, and extortion, primarily targets individual decision-making processes (Louderback and Antonaccio, 2017), often without exploiting any software vulnerability at all. Consequently, the investigative needs of cybercrime differ substantially from those of traditional cyberattacks.

In the intensive care unit, the underlying causes of critical illness vary substantially across diagnoses, yet prediction models accounting for diagnostic heterogeneity have not been systematically studied. To address the gap, we evaluate transfer learning approaches for diagnosis-specific mortality prediction and apply both GLM- and XGBoost-based models to the eICU Collaborative Research Database. Our results demonstrate that transfer learning consistently outperforms models trained only on diagnosis-specific data and those using a well-known ICU severity-of-illness score, i.e., APACHE IVa, alone, while also achieving better calibration than models trained on the pooled data. Our findings also suggest that the Youden cutoff is a more appropriate decision threshold than the conventional 0.5 for binary outcomes, and that transfer learning maintains consistently high predictive performance across various cutoff criteria.

Understanding the dynamic reorganization of brain networks is critical for predicting cognitive decline, neurological progression, and individual variability in clinical outcomes. This work proposes a multimodal graph neural network framework that integrates structural MRI, diffusion tensor imaging, and functional MRI to model spatiotemporal brain network reorganization. Brain regions are represented as nodes and structural and functional connectivity as edges, forming longitudinal brain graphs for each subject. Temporal evolution is captured via fractional stochastic differential operators embedded within graph-based recurrent networks, enabling the modeling of long-term dependencies and stochastic fluctuations in network dynamics. Attention mechanisms fuse multimodal information and generate interpretable biomarkers, including network energy entropy, graph curvature, fractional memory indices, and modality-specific attention scores. These biomarkers are combined into a composite prognostic index to quantify individual risk of network instability or cognitive decline. Experiments on longitudinal neuroimaging datasets demonstrate both predictive accuracy and interpretability. The results highlight the potential of mathematically rigorous, multimodal graph-based approaches for deriving clinically meaningful biomarkers from existing imaging data without requiring new data collection.

This paper proposes using the Linux kernel ftrace framework, particularly the function graph tracer, to generate informative system level data for machine learning (ML) applications. Experiments on a real world encryption detection task demonstrate the efficacy of the proposed features across several learning algorithms. The learner faces the problem of detecting encryption activities across a large dataset of files, using function call traces and graph based features. Empirical results highlight an outstanding accuracy of 99.28 on the task at hand, underscoring the efficacy of features derived from the function graph tracer. The results were further validated in an additional experiment targeting a multilabel classification problem, in which running programs were identified from trace data. This work provides comprehensive methodologies for preprocessing raw trace data and extracting graph based features, offering significant advancements in applying ML to system behavior analysis, program identification, and anomaly detection. By bridging the gap between system tracing and ML, this paper paves the way for innovative solutions in performance monitoring and security analytics.

Early detection of cancer plays a key role in improving survival rates, but identifying reliable biomarkers from RNA-seq data is still a major challenge. The data are high-dimensional, and conventional statistical methods often fail to capture the complex relationships between genes. In this study, we introduce RGE-GCN (Recursive Gene Elimination with Graph Convolutional Networks), a framework that combines feature selection and classification in a single pipeline. Our approach builds a graph from gene expression profiles, uses a Graph Convolutional Network to classify cancer versus normal samples, and applies Integrated Gradients to highlight the most informative genes. By recursively removing less relevant genes, the model converges to a compact set of biomarkers that are both interpretable and predictive. We evaluated RGE-GCN on synthetic data as well as real-world RNA-seq cohorts of lung, kidney, and cervical cancers. Across all datasets, the method consistently achieved higher accuracy and F1-scores than standard tools such as DESeq2, edgeR, and limma-voom. Importantly, the selected genes aligned with well-known cancer pathways including PI3K-AKT, MAPK, SUMOylation, and immune regulation. These results suggest that RGE-GCN shows promise as a generalizable approach for RNA-seq based early cancer detection and biomarker discovery (https://rce-gcn.streamlit.app/ ).

The global rise in type 2 diabetes underscores the need for scalable and cost-effective screening methods. Current diagnosis requires biochemical assays, which are invasive and costly. Advances in consumer wearables have enabled early explorations of machine learning-based disease detection, but prior studies were limited to controlled settings. We present SweetDeep, a compact neural network trained on physiological and demographic data from 285 (diabetic and non-diabetic) participants in the EU and MENA regions, collected using Samsung Galaxy Watch 7 devices in free-living conditions over six days. Each participant contributed multiple 2-minute sensor recordings per day, totaling approximately 20 recordings per individual. Despite comprising fewer than 3,000 parameters, SweetDeep achieves 82.5% patient-level accuracy (82.1% macro-F1, 79.7% sensitivity, 84.6% specificity) under three-fold cross-validation, with an expected calibration error of 5.5%. Allowing the model to abstain on less than 10% of low-confidence patient predictions yields an accuracy of 84.5% on the remaining patients. These findings demonstrate that combining engineered features with lightweight architectures can support accurate, rapid, and generalizable detection of type 2 diabetes in real-world wearable settings.

Abstract--The widespread adoption of large language models (LLMs) has made it difficult to distinguish human writing from machine-produced text in many real applications. Detectors that were effective for one generation of models tend to degrade when newer models or modified decoding strategies are introduced. In this work, we study this lack of stability and propose a hybrid ensemble that is explicitly designed to cope with changing generator distributions. The ensemble combines three complementary components: a RoBERT a-based classifier fine-tuned for supervised detection, a curvature-inspired score based on perturbing the input and measuring changes in model likelihood, and a compact stylometric model built on handcrafted linguistic features. The outputs of these components are fused on the probability simplex, and the weights are chosen via validation-based search. We frame this approach in terms of variance reduction and risk under mixtures of generators, and show that the simplex constraint provides a simple way to trade off the strengths and weaknesses of each branch. Experiments on a 30 000-document corpus drawn from several LLM families including models unseen during training and paraphrased attack variants show that the proposed method achieves 94.2% accuracy and an AUC of 0.978. The ensemble also lowers false positives on scientific articles compared to strong baselines, which is critical in educational and research settings where wrongly flagging human work is costly. Text generated by large language models (LLMs) is now routinely used in homework, reports, programming, and informal communication.

Existing Grammatical Error Correction (GEC) systems suffer from limited reference diversity, leading to underestimated evaluation and restricted model generalization. To address this issue, we introduce the Judge of Edit-Level Validity (JELV), an automated framework to validate correction edits from grammaticality, faithfulness, and fluency. Using our proposed human-annotated Pair-wise Edit-level Validity Dataset (PEVData) as benchmark, JELV offers two implementations: a multi-turn LLM-as-Judges pipeline achieving 90% agreement with human annotators, and a distilled DeBERTa classifier with 85% precision on valid edits. We then apply JELV to reclassify misjudged false positives in evaluation and derive a comprehensive evaluation metric by integrating false positive decoupling and fluency scoring, resulting in state-of-the-art correlation with human judgments. We also apply JELV to filter LLM-generated correction candidates, expanding the BEA19's single-reference dataset containing 38,692 source sentences. Retraining top GEC systems on this expanded dataset yields measurable performance gains. JELV provides a scalable solution for enhancing reference diversity and strengthening both evaluation and model generalization.

Detecting regime shifts in chaotic time series is difficult because observation-space signals are entangled with intrinsic variability. We propose Parameter-Space Changepoint Detection (Param-CPD), a two-stage framework that first amortizes Bayesian inference of governing parameters with a neural posterior estimator trained by simulation-based inference, and then applies a standard CPD algorithm to the resulting parameter trajectory. In Lorenz-63 with piecewise-constant parameters, Param-CPD improves F1, reduces localization error, and reduces false positives compared to baselines of observation-space. We further verify identifiability and calibration of the inferred posteriors on stationary trajectories, explaining why parameter space offers a cleaner detection signal. Robustness analyzes of tolerance, window length, and noise indicate consistent gains. Our results show that operating in a physically interpretable parameter space enables accurate and interpretable changepoint detection in nonlinear dynamical systems.

Universal multimodal embedding models are foundational to various tasks. Existing approaches typically employ in-batch negative mining by measuring the similarity of query-candidate pairs. However, these methods often struggle to capture subtle semantic differences among candidates and lack diversity in negative samples. Moreover, the embeddings exhibit limited discriminative ability in distinguishing false and hard negatives. In this paper, we leverage the advanced understanding capabilities of MLLMs to enhance representation learning and present a novel Universal Multimodal Embedding (UniME-V2) model. Our approach first constructs a potential hard negative set through global retrieval. We then introduce the MLLM-as-a-Judge mechanism, which utilizes MLLMs to assess the semantic alignment of query-candidate pairs and generate soft semantic matching scores. These scores serve as a foundation for hard negative mining, mitigating the impact of false negatives and enabling the identification of diverse, high-quality hard negatives. Furthermore, the semantic matching scores are used as soft labels to mitigate the rigid one-to-one mapping constraint. By aligning the similarity matrix with the soft semantic matching score matrix, the model learns semantic distinctions among candidates, significantly enhancing its discriminative capacity. To further improve performance, we propose UniME-V2-Reranker, a reranking model trained on our mined hard negatives through a joint pairwise and listwise optimization approach. We conduct comprehensive experiments on the MMEB benchmark and multiple retrieval tasks, demonstrating that our method achieves state-of-the-art performance on average across all tasks.