Active Learning (AL) deals with identifying the most informative samples for labeling to reduce data annotation costs for supervised learning tasks. AL research suffers from the fact that lifts from literature generalize poorly and that only a small number of repetitions of experiments are conducted. To overcome these obstacles, we propose CDALBench, the first active learning benchmark which includes tasks in computer vision, natural language processing and tabular learning. Furthermore, by providing an efficient, greedy oracle, CDALBench can be evaluated with 50 runs for each experiment. We show, that both the cross-domain character and a large amount of repetitions are crucial for sophisticated evaluation of AL research. Concretely, we show that the superiority of specific methods varies over the different domains, making it important to evaluate Active Learning with a cross-domain benchmark. Additionally, we show that having a large amount of runs is crucial. With only conducting three runs as often done in the literature, the superiority of specific methods can strongly vary with the specific runs. This effect is so strong, that, depending on the seed, even a well-established method's performance can be significantly better and significantly worse than random for the same dataset.

Objectives: To evaluate GPT-4o's ability to extract diagnostic labels (with uncertainty) from free-text radiology reports and to test how these labels affect multi-label image classification of musculoskeletal radiographs. Methods: This retrospective study included radiography series of the clavicle (n=1,170), elbow (n=3,755), and thumb (n=1,978). After anonymization, GPT-4o filled out structured templates by indicating imaging findings as present ("true"), absent ("false"), or "uncertain." To assess the impact of label uncertainty, "uncertain" labels of the training and validation sets were automatically reassigned to "true" (inclusive) or "false" (exclusive). Label-image-pairs were used for multi-label classification using ResNet50. Label extraction accuracy was manually verified on internal (clavicle: n=233, elbow: n=745, thumb: n=393) and external test sets (n=300 for each). Performance was assessed using macro-averaged receiver operating characteristic (ROC) area under the curve (AUC), precision recall curves, sensitivity, specificity, and accuracy. AUCs were compared with the DeLong test. Results: Automatic extraction was correct in 98.6% (60,618 of 61,488) of labels in the test sets. Across anatomic regions, label-based model training yielded competitive performance measured by macro-averaged AUC values for inclusive (e.g., elbow: AUC=0.80 [range, 0.62-0.87]) and exclusive models (elbow: AUC=0.80 [range, 0.61-0.88]). Models generalized well on external datasets (elbow [inclusive]: AUC=0.79 [range, 0.61-0.87]; elbow [exclusive]: AUC=0.79 [range, 0.63-0.89]). No significant differences were observed across labeling strategies or datasets (p>=0.15). Conclusion: GPT-4o extracted labels from radiologic reports to train competitive multi-label classification models with high accuracy. Detected uncertainty in the radiologic reports did not influence the performance of these models.

Risk prediction that capitalizes on emerging genetic findings holds great promise for improving public health and clinical care. However, recent risk prediction research has shown that predictive tests formed on existing common genetic loci, including those from genome-wide association studies, have lacked sufficient accuracy for clinical use. Because most rare variants on the genome have not yet been studied for their role in risk prediction, future disease prediction discoveries should shift toward a more comprehensive risk prediction strategy that takes into account both common and rare variants. We are proposing a collapsing receiver operating characteristic CROC approach for risk prediction research on both common and rare variants. The new approach is an extension of a previously developed forward ROC FROC approach, with additional procedures for handling rare variants. The approach was evaluated through the use of 533 single-nucleotide polymorphisms SNPs in 37 candidate genes from the Genetic Analysis Workshop 17 mini-exome data set. We found that a prediction model built on all SNPs gained more accuracy AUC = 0.605 than one built on common variants alone AUC = 0.585. We further evaluated the performance of two approaches by gradually reducing the number of common variants in the analysis. We found that the CROC method attained more accuracy than the FROC method when the number of common variants in the data decreased. In an extreme scenario, when there are only rare variants in the data, the CROC reached an AUC value of 0.603, whereas the FROC had an AUC value of 0.524.

Cardiovascular diseases (CVDs) are the leading cause of mortality worldwide, accounting for over 30% of global deaths according to the World Health Organization (WHO). Importantly, one-third of these deaths are preventable with timely and accurate diagnosis. The electrocardiogram (ECG), a non-invasive method for recording the electrical activity of the heart, is crucial for diagnosing CVDs. However, privacy concerns surrounding the use of patient ECG data in research have spurred interest in synthetic data, which preserves the statistical properties of real data without compromising patient confidentiality. This study explores the potential of synthetic ECG data for training deep learning models from regression to classification tasks and evaluates the feasibility of transfer learning to enhance classification performance on real ECG data. We experimented with popular deep learning models to predict four key cardiac parameters, namely, Heart Rate (HR), PR interval, QT interval, and QRS complex-using separate regression models. Subsequently, we leveraged these regression models for transfer learning to perform 5-class ECG signal classification. Our experiments systematically investigate whether transfer learning from regression to classification is viable, enabling better utilization of diverse open-access and synthetic ECG datasets. Our findings demonstrate that transfer learning from regression to classification improves classification performance, highlighting its potential to maximize the utility of available data and advance deep learning applications in this domain.

Transformers have profoundly influenced AI research, but explaining their decisions remains challenging -- even for relatively simpler tasks such as classification -- which hinders trust and safe deployment in real-world applications. Although activation-based attribution methods effectively explain transformer-based text classification models, our findings reveal that these methods can be undermined by class-irrelevant features within activations, leading to less reliable interpretations. To address this limitation, we propose Contrast-CAT, a novel activation contrast-based attribution method that refines token-level attributions by filtering out class-irrelevant features. By contrasting the activations of an input sequence with reference activations, Contrast-CAT generates clearer and more faithful attribution maps. Experimental results across various datasets and models confirm that Contrast-CAT consistently outperforms state-of-the-art methods. Notably, under the MoRF setting, it achieves average improvements of x1.30 in AOPC and x2.25 in LOdds over the most competing methods, demonstrating its effectiveness in enhancing interpretability for transformer-based text classification.

Insulin resistance (IR) is a key precursor to diabetes and a significant risk factor for cardiovascular disease. Traditional IR assessment methods require multiple blood tests. We developed a simple AI model using only fasting blood glucose to predict IR in non-diabetic populations. Data from the NHANES (1999-2020) and CHARLS (2015) studies were used for model training and validation. Input features included age, gender, height, weight, blood pressure, waist circumference, and fasting blood glucose. The CatBoost algorithm achieved AUC values of 0.8596 (HOMA-IR) and 0.7777 (TyG index) in NHANES, with an external AUC of 0.7442 for TyG. For METS-IR prediction, the model achieved AUC values of 0.9731 (internal) and 0.9591 (external), with RMSE values of 3.2643 (internal) and 3.057 (external). SHAP analysis highlighted waist circumference as a key predictor of IR. This AI model offers a minimally invasive and effective tool for IR prediction, supporting early diabetes and cardiovascular disease prevention.

It is widely accepted that the Bayesian ideal observer (IO) should be used to guide the objective assessment and optimization of medical imaging systems. The IO employs complete task-specific information to compute test statistics for making inference decisions and performs optimally in signal detection tasks. However, the IO test statistic typically depends non-linearly on the image data and cannot be analytically determined. The ideal linear observer, known as the Hotelling observer (HO), can sometimes be used as a surrogate for the IO. However, when image data are high dimensional, HO computation can be difficult. Efficient channels that can extract task-relevant features have been investigated to reduce the dimensionality of image data to approximate IO and HO performance. This work proposes a novel method for generating efficient channels by use of the gradient of a Lagrangian-based loss function that was designed to learn the HO. The generated channels are referred to as the Lagrangian-gradient (L-grad) channels. Numerical studies are conducted that consider binary signal detection tasks involving various backgrounds and signals. It is demonstrated that channelized HO (CHO) using L-grad channels can produce significantly better signal detection performance compared to the CHO using PLS channels. Moreover, it is shown that the proposed L-grad method can achieve significantly lower computation time compared to the PLS method.

The rapid expansion of citizen science initiatives has led to a significant growth of biodiversity databases, and particularly presence-only (PO) observations. PO data are invaluable for understanding species distributions and their dynamics, but their use in a Species Distribution Model (SDM) is curtailed by sampling biases and the lack of information on absences. Poisson point processes are widely used for SDMs, with Maxent being one of the most popular methods. Maxent maximises the entropy of a probability distribution across sites as a function of predefined transformations of variables, called features. In contrast, neural networks and deep learning have emerged as a promising technique for automatic feature extraction from complex input variables. Arbitrarily complex transformations of input variables can be learned from the data efficiently through backpropagation and stochastic gradient descent (SGD). In this paper, we propose DeepMaxent, which harnesses neural networks to automatically learn shared features among species, using the maximum entropy principle. To do so, it employs a normalised Poisson loss where for each species, presence probabilities across sites are modelled by a neural network. We evaluate DeepMaxent on a benchmark dataset known for its spatial sampling biases, using PO data for calibration and presence-absence (PA) data for validation across six regions with different biological groups and covariates. Our results indicate that DeepMaxent performs better than Maxent and other leading SDMs across all regions and taxonomic groups. The method performs particularly well in regions of uneven sampling, demonstrating substantial potential to increase SDM performances. In particular, our approach yields more accurate predictions than traditional single-species models, which opens up new possibilities for methodological enhancement.

MRI and CT are essential clinical cross-sectional imaging techniques for diagnosing complex conditions. However, large 3D datasets with annotations for deep learning are scarce. While methods like DINOv2 are encouraging for 2D image analysis, these methods have not been applied to 3D medical images. Furthermore, deep learning models often lack explainability due to their "black-box" nature. This study aims to extend 2D self-supervised models, specifically DINOv2, to 3D medical imaging while evaluating their potential for explainable outcomes. We introduce the Medical Slice Transformer (MST) framework to adapt 2D self-supervised models for 3D medical image analysis. MST combines a Transformer architecture with a 2D feature extractor, i.e., DINOv2. We evaluate its diagnostic performance against a 3D convolutional neural network (3D ResNet) across three clinical datasets: breast MRI (651 patients), chest CT (722 patients), and knee MRI (1199 patients). Both methods were tested for diagnosing breast cancer, predicting lung nodule dignity, and detecting meniscus tears. Diagnostic performance was assessed by calculating the Area Under the Receiver Operating Characteristic Curve (AUC). Explainability was evaluated through a radiologist's qualitative comparison of saliency maps based on slice and lesion correctness. P-values were calculated using Delong's test. MST achieved higher AUC values compared to ResNet across all three datasets: breast (0.94$\pm$0.01 vs. 0.91$\pm$0.02, P=0.02), chest (0.95$\pm$0.01 vs. 0.92$\pm$0.02, P=0.13), and knee (0.85$\pm$0.04 vs. 0.69$\pm$0.05, P=0.001). Saliency maps were consistently more precise and anatomically correct for MST than for ResNet. Self-supervised 2D models like DINOv2 can be effectively adapted for 3D medical imaging using MST, offering enhanced diagnostic accuracy and explainability compared to convolutional neural networks.

This study investigates the impact of quantity and diversity of data on the performance of various machine-learning models for detecting general EEG pathology. We utilized an EEG dataset of 2,993 recordings from Temple University Hospital and a dataset of 55,787 recordings from Elmiko Biosignals sp. z o.o. The latter contains data from 39 hospitals and a diverse patient set with varied conditions. Thus, we introduce the Elmiko dataset - the largest publicly available EEG corpus. Our findings show that small and consistent datasets enable a wide range of models to achieve high accuracy; however, variations in pathological conditions, recording protocols, and labeling standards lead to significant performance degradation. Nonetheless, increasing the number of available recordings improves predictive accuracy and may even compensate for data diversity, particularly in neural networks based on attention mechanism or transformer architecture. A meta-model that combined these networks with a gradient-boosting approach using handcrafted features demonstrated superior performance across varied datasets.