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.

This study presents a pipeline leveraging t-Distributed Stochastic Neighbor Embedding (t-SNE) for interpretable visualizations of chirp features across diverse outcome scenarios. The dataset, comprising chirp-based temporal, spectral, and frequency metrics. Using t-SNE, local neighborhood relationships were preserved while addressing the crowding problem through Student t-distribution-based similarity optimization. Three classification tasks were formulated on the 2D t-SNE embeddings: (1) distinguishing clinical success from failure/no-resection, (2) separating high-difficulty from low-difficulty cases, and (3) identifying optimal cases, defined as successful outcomes with minimal clinical difficulty. Four classifiers, namely, Random Forests, Support Vector Machines, Logistic Regression, and k-Nearest Neighbors, were trained and evaluated using stratified 5-fold cross-validation. Across tasks, the Random Forest and k-NN classifiers demonstrated superior performance, achieving up to 88.8% accuracy in optimal case detection (successful outcomes with minimal clinical difficulty). Additionally, feature influence sensitivity maps were generated using SHAP explanations applied to model predicting t-SNE coordinates, revealing spatially localized feature importance within the embedding space. These maps highlighted how specific chirp attributes drive regional clustering and class separation, offering insights into the latent structure of the data. The integrated framework showcases the potential of interpretable embeddings and local feature attribution for clinical stratification and decision support.

Estimating disease severity from endoscopic images is essential in assessing ulcerative colitis, where the Mayo Endoscopic Subscore (MES) is widely used to grade inflammation. However, MES classification remains challenging due to label noise from inter-observer variability and the ordinal nature of the score, which standard models often ignore. We propose CLoE, a curriculum learning framework that accounts for both label reliability and ordinal structure. Image quality, estimated via a lightweight model trained on Boston Bowel Preparation Scale (BBPS) labels, is used as a proxy for annotation confidence to order samples from easy (clean) to hard (noisy). This curriculum is further combined with ResizeMix augmentation to improve robustness. Experiments on the LIMUC and HyperKvasir datasets, using both CNNs and Transformers, show that CLoE consistently improves performance over strong supervised and self-supervised baselines. For instance, ConvNeXt-Tiny reaches 82.5\% accuracy and a QWK of 0.894 on LIMUC with low computational cost. These results highlight the potential of difficulty-aware training strategies for improving ordinal classification under label uncertainty. Code will be released at https://github.com/zeynepozdemir/CLoE.

In fact, a line of work has proposed to learn group-invariant representations with adversarial learning techniques in order to achieve statistical parity, also known as the demographic parity in the literature.

Existing state-of-the-art dense object detection techniques tend to produce a large number of false positive detections on difficult images with complex scenes because they focus on ensuring a high recall. To improve the detection accuracy, we propose an Adaptive Important Region Selection ( AIRS) framework guided by Evidential Q-learning coupled with a uniquely designed reward function. Inspired by human visual attention, our detection model conducts object search in a top-down, hierarchical fashion. It starts from the top of the hierarchy with the coarsest granularity and then identifies the potential patches likely to contain objects of interest. It then discards non-informative patches and progressively moves downward on the selected ones for a fine-grained search. The proposed evidential Q-learning systematically encodes epistemic uncertainty in its evidential-Q value to encourage the exploration of unknown patches, especially in the early phase of model training. In this way, the proposed model dynamically balances exploration-exploitation to cover both highly valuable and informative patches. Theoretical analysis and extensive experiments on multiple datasets demonstrate that our proposed framework outperforms the SOT A models.

Nonetheless, most of the existing methods could only optimize P AUC approximately, leading to inevitable biases that are not controllable.

Prompted by these insights, we reviewed over 1.5 million scientific papers to understand the origin of this invalid