arXiv subjects

Nabil Ashab

Publications and source records attributed to Nabil Ashab.

3 recordsLinked to original sources

arXiv2026

ORViT-DR: Ordinally-Robust Hybrid ViT for Low-Resolution Diabetic Retinopathy Grading

Diabetic retinopathy (DR) is one of the main causes of impaired vision. A good and reliable automated grading system can make the screening process safer and more accurate. Because DR stages progress gradually, the task of grading disease severity naturally follows an ordinal structure in which neighboring classes share similar visual characteristics. In this study, ORViT-DR, a hybrid deep learning framework, is designed to improve DR grading from low-resolution retinal images. The proposed approach combines convolutional feature extraction with transformer-based global context modeling through a pre-trained ViT-Hybrid backbone, which integrates BiT-ResNetv2 with a Vision Transformer architecture. The approach is tested on the RetinaMNIST subset of the MedMNISTv2 dataset, which contains 28x28 retinal fundus images annotated with five levels of disease severity. To promote stable training and better feature learning, the training strategy applies progressive layer unfreezing, layer-wise learning rate decay, exponential moving average (EMA) parameter updates, and ensemble-based prediction during inference. Experimental results on the official RetinaMNIST test set show that the proposed method achieves 57.00% classification accuracy, along with a quadratic weighted kappa score of 0.5963 and a macro-F1 score of 0.4293. These results suggest that hybrid CNN-Transformer architectures can provide effective representations for ordinal retinal image analysis.

eess.IV↗

arXiv2026

MagViT: Interpretable Multi-Magnification Transformers with Patient-Level Model Selection for Breast Histopathology

Breast cancer is one of the most common types of cancer among women around the world. Rapid detection and early treatment can hinder its progress to more complex stages and can impede its spread to other parts of the body. Histopathological image classification is the most common task in cancer detection due to its robustness in analyzing cellular data. Breast histopathology classification requires handling both multi-scale tissue morphology and clinically relevant generalization beyond the source domain. This paper presents MagViT, an interpretable multi-magnification transformer framework with scale-gated fusion and patient-level model selection. The model uses four BreakHis magnifications (40X, 100X, 200X, 400X) and extracts per-scale representations with a ViT backbone, and combines them via a learnable gate that masks missing scales. Patient-level five-fold cross-validation with a fixed seed has been run and compared with three architectural branches. The most accurate branch is then selected as the final model due to the strongest patient-level accuracy while retaining the simplest fusion pathway. On BreakHis, our architecture achieves a mean image accuracy of 0.9191, a mean patient accuracy of 0.9643, and a mean macro-F1 of 0.9042. External transfer experiments provide preliminary evidence of cross-dataset generalization under controlled adaptation settings on BUSI (image accuracy 0.8306, macro-F1 0.7480, patient accuracy 0.8291) and IDC (image accuracy 0.8577, macro-F1 0.8191, patient accuracy 0.8372). Grad-CAM visualization indicates that the model focuses on diagnostically significant and meaningful regions across magnifications. Relative to prior ViT-centered BreakHis work, this study emphasizes patient-level selection and cross-dataset robustness under a reproducible protocol.

eess.IV↗

arXiv2026

Few-Shot Cross-Dataset Adaptation for Tuberculosis Detection Using DenseNet

Tuberculosis (TB) is one of the most common and dangerous bacterial ailments. Every year, it causes a large number of deaths worldwide. Although many deep learning models can detect tuberculosis from chest X-rays quite accurately, severe domain shift across datasets makes the task challenging. Different imaging protocols, patient demographics, and equipment across domains make the task of generalization difficult. In real-world settings, a model may perform well on one dataset but show a noticeable drop in performance when tested on another. In this work, we address this domain adaptation challenge through a few-shot scaling study. A controlled cross-dataset evaluation is presented in this paper using TBX11K as the source domain and the Mendeley TB dataset as the target domain. It is investigated how varying the number of target samples affects model performance under three training regimes: frozen backbone adaptation, full fine-tuning of a source-pretrained DenseNet121 model, and training from scratch. The results indicate that the model can perform well even with limited data and can achieve 98.36\% accuracy with just 75 labeled samples per class. The adaptation curves demonstrate how fine-tuning effectively mitigates domain shift. These findings establish full fine-tuning of pretrained models as a highly effective and practical strategy for mitigating domain shift in low-resource clinical deployment scenarios.

cs.CV↗