Infertility is a major global health issue, and while in-vitro fertilization has improved treatment outcomes, embryo selection remains a critical bottleneck. Time-lapse imaging enables continuous, non-invasive monitoring of embryo development, yet most automated assessment methods rely solely on conventional morphokinetic features and overlook emerging biomarkers. Cytoplasmic Strings, thin filamentous structures connecting the inner cell mass and trophectoderm in expanded blastocysts, have been associated with faster blastocyst formation, higher blastocyst grades, and improved viability. However, CS assessment currently depends on manual visual inspection, which is labor-intensive, subjective, and severely affected by detection and subtle visual appearance. In this work, we present, to the best of our knowledge, the first computational framework for CS analysis in human IVF embryos. We first design a human-in-the-loop annotation pipeline to curate a biologically validated CS dataset from TLI videos, comprising 13,568 frames with highly sparse CS-positive instances. Building on this dataset, we propose a two-stage deep learning framework that (i) classifies CS presence at the frame level and (ii) localizes CS regions in positive cases. To address severe imbalance and feature uncertainty, we introduce the Novel Uncertainty-aware Contractive Embedding (NUCE) loss, which couples confidence-aware reweighting with an embedding contraction term to form compact, well-separated class clusters. NUCE consistently improves F1-score across five transformer backbones, while RF-DETR-based localization achieves state-of-the-art (SOTA) detection performance for thin, low-contrast CS structures. The source code will be made publicly available at: https://github.com/HamadYA/CS_Detection.

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.

Large-scale generative models have shown impressive image-generation capabilities, propelled by massive data.

We propose a novel continual self-supervised learning (CSSL) framework for simultaneously learning diverse features from multi-window-obtained chest computed tomography (CT) images and ensuring data privacy. Achieving a robust and highly generalizable model in medical image diagnosis is challenging, mainly because of issues, such as the scarcity of large-scale, accurately annotated datasets and domain shifts inherent to dynamic healthcare environments. Specifically, in chest CT, these domain shifts often arise from differences in window settings, which are optimized for distinct clinical purposes. Previous CSSL frameworks often mitigated domain shift by reusing past data, a typically impractical approach owing to privacy constraints. Our approach addresses these challenges by effectively capturing the relationship between previously learned knowledge and new information across different training stages through continual pretraining on unlabeled images. Specifically, by incorporating a latent replay-based mechanism into CSSL, our method mitigates catastrophic forgetting due to domain shifts during continual pretraining while ensuring data privacy. Additionally, we introduce a feature distillation technique that integrates Wasserstein distance-based knowledge distillation (WKD) and batch-knowledge ensemble (BKE), enhancing the ability of the model to learn meaningful, domain-shift-robust representations. Finally, we validate our approach using chest CT images obtained across two different window settings, demonstrating superior performance compared with other approaches.

Here we present a new class of optimality for coding systems. Members of that class are displaced linearly from optimal coding and thus exhibit Zipf's law, namely a power-law distribution of frequency ranks. Within that class, Zipf's law, the size-rank law and the size-probability law form a group-like structure. We identify human languages that are members of the class. All languages showing sufficient agreement with Zipf's law are potential members of the class. In contrast, there are communication systems in other species that cannot be members of that class for exhibiting an exponential distribution instead but dolphins and humpback whales might. We provide a new insight into plots of frequency versus rank in double logarithmic scale. For any system, a straight line in that scale indicates that the lengths of optimal codes under non-singular coding and under uniquely decodable encoding are displaced by a linear function whose slope is the exponent of Zipf's law. For systems under compression and constrained to be uniquely decodable, such a straight line may indicate that the system is coding close to optimality. We provide support for the hypothesis that Zipf's law originates from compression and define testable conditions for the emergence of Zipf's law in compressing systems.

Large-scale generative models have shown impressive image-generation capabilities, propelled by massive data.

Future high-luminosity hadron colliders demand tracking detectors with extreme radiation tolerance, high spatial precision, and sub-nanosecond timing. 3D diamond pixel sensors offer these capabilities due to diamond's radiation hardness and high carrier mobility. Conductive electrodes, produced via femtosecond IR laser pulses, exhibit high resistivity that delays signal propagation. This effect necessitates extending the classical Ramo-Shockley weighting potential formalism. We model the phenomenon through a 3rd-order, 3+1D PDE derived as a quasi-stationary approximation of Maxwell's equations. The PDE is solved numerically and coupled with charge transport simulations for realistic 3D sensor geometries. A Mixture-of-Experts Physics-Informed Neural Network, trained on Spectral Method data, provides a meshless solver to assess timing degradation from electrode resistance.

Generative adversarial networks (GANs) and diffusion models have dramatically advanced deepfake technology, and its threats to digital security, media integrity, and public trust have increased rapidly. This research explored zero-shot deepfake detection, an emerging method even when the models have never seen a particular deepfake variation. In this work, we studied self-supervised learning, transformer-based zero-shot classifier, generative model fingerprinting, and meta-learning techniques that better adapt to the ever-evolving deepfake threat. In addition, we suggested AI-driven prevention strategies that mitigated the underlying generation pipeline of the deepfakes before they occurred. They consisted of adversarial perturbations for creating deepfake generators, digital watermarking for content authenticity verification, real-time AI monitoring for content creation pipelines, and blockchain-based content verification frameworks. Despite these advancements, zero-shot detection and prevention faced critical challenges such as adversarial attacks, scalability constraints, ethical dilemmas, and the absence of standardized evaluation benchmarks. These limitations were addressed by discussing future research directions on explainable AI for deepfake detection, multimodal fusion based on image, audio, and text analysis, quantum AI for enhanced security, and federated learning for privacy-preserving deepfake detection. This further highlighted the need for an integrated defense framework for digital authenticity that utilized zero-shot learning in combination with preventive deepfake mechanisms. Finally, we highlighted the important role of interdisciplinary collaboration between AI researchers, cybersecurity experts, and policymakers to create resilient defenses against the rising tide of deepfake attacks.

Fragment-Based Drug Discovery (FBDD) is a popular approach in early drug development, but designing effective linkers to combine disconnected molecular fragments into chemically and pharmacologically viable candidates remains challenging. Further complexity arises when fragments contain structural redundancies, like duplicate rings, which cannot be addressed by simply adding or removing atoms or bonds. To address these challenges in a unified framework, we introduce FragmentGPT, which integrates two core components: (1) a novel chemically-aware, energy-based bond cleavage pre-training strategy that equips the GPT-based model with fragment growing, linking, and merging capabilities, and (2) a novel Reward Ranked Alignment with Expert Exploration (RAE) algorithm that combines expert imitation learning for diversity enhancement, data selection and augmentation for Pareto and composite score optimality, and Supervised Fine-Tuning (SFT) to align the learner policy with multi-objective goals. Conditioned on fragment pairs, FragmentGPT generates linkers that connect diverse molecular subunits while simultaneously optimizing for multiple pharmaceutical goals. It also learns to resolve structural redundancies-such as duplicated fragments-through intelligent merging, enabling the synthesis of optimized molecules. FragmentGPT facilitates controlled, goal-driven molecular assembly. Experiments and ablation studies on real-world cancer datasets demonstrate its ability to generate chemically valid, high-quality molecules tailored for downstream drug discovery tasks.

Operator learning has emerged as a promising tool for accelerating the solution of partial differential equations (PDEs). The Deep Operator Networks (DeepONets) represent a pioneering framework in this area: the "vanilla" DeepONet is valued for its simplicity and efficiency, while the modified DeepONet achieves higher accuracy at the cost of increased training time. In this work, we propose a series of Transformer-inspired DeepONet variants that introduce bidirectional cross-conditioning between the branch and trunk networks in DeepONet. Query-point information is injected into the branch network and input-function information into the trunk network, enabling dynamic dependencies while preserving the simplicity and efficiency of the "vanilla" DeepONet in a non-intrusive manner. Experiments on four PDE benchmarks -- advection, diffusion-reaction, Burgers', and Korteweg-de Vries equations -- show that for each case, there exists a variant that matches or surpasses the accuracy of the modified DeepONet while offering improved training efficiency. Moreover, the best-performing variant for each equation aligns naturally with the equation's underlying characteristics, suggesting that the effectiveness of cross-conditioning depends on the characteristics of the equation and its underlying physics. To ensure robustness, we validate the effectiveness of our variants through a range of rigorous statistical analyses, among them the Wilcoxon Two One-Sided Test, Glass's Delta, and Spearman's rank correlation.