Augmentations that model the physical causes of domain shift improve cross-source transfer at no cost to in-domain accuracy, and the improvement survives a selection-disjoint, contamination-free evaluation.
Abstract
Background/Objectives: Dermoscopic skin-lesion classifiers lose accuracy when images arrive from a new clinic or a new device. We asked which data augmentations reduce that loss, and measured the effect under a protocol that keeps policy selection separate from policy evaluation. Methods: A ConvNeXt-Large binary malignant-versus-non-malignant classifier was trained on six dermoscopic sources (25,903 images); HAM10000 and ISIC 2016-2020 were held out of training entirely. Single augmentations, photometric combinations and eleven composite policies were ranked on a development split of 1511 held-out images. The winning policy was then evaluated on a confirmation set of 8073 held-out images that took no part in that ranking and from which we removed every image sharing a lesion identifier with the training data and every image contributed by an institution represented in training. Both policies were retrained with four random seeds each and compared with an exact permutation test. Results: The mix policy raised confirmation-set ROC-AUC from 0.787 to 0.826 (+0.039; per-seed ranges 0.772-0.797 and 0.815-0.840, non-overlapping; exact permutation p=0.029), with the same direction on each contributing source. At matched sensitivity the gain is larger in clinical terms: specificity rose from 0.612 to 0.713 at a sensitivity of 0.80, and from 0.284 to 0.397 at a sensitivity of 0.95. In-domain ROC-AUC was preserved (0.938 to 0.941). On an independent clinical cohort acquired with a different device at a different institution (472 images, 22 malignant), performance was maintained (0.934 versus 0.930). Conclusions: Augmentations that model the physical causes of domain shift improve cross-source transfer at no cost to in-domain accuracy, and the improvement survives a selection-disjoint, contamination-free evaluation.
Background/Objectives: Cutaneous melanoma caused over 331,000 new cases and 58,000 deaths worldwide in 2022, with five-year survival falling from 99.4% in localised disease to 35.6% after distant metastasis. Most dermoscopic deep learning studies report headline accuracy without addressing data leakage, calibration, or...
Abdulvahap Pınar, F. H. Yagin, Cemil Çolak et al.· Journal of Clinical Medicine· 0 citations
Early assessment of suspicious skin lesions can improve access to care, but dermoscopic interpretation depends on specialist expertise and automated classifiers must be evaluated carefully under severe class imbalance. This paper presents a seven-class convolutional neural network pipeline and a cloud-connected desktop...
Yazeed Al Moaiad, Marwan Ehssi· International Journal on Con...· 0 citations
An ensemble model combining EfficientNetB3 and Xception, trained using transfer learning with ImageNet weights with SMOTE-based balancing, offers a reliable solution for automated skin cancer classification.
Shabib Aftab, Tuba Mubarik, M. A. Saeed· International Journal of Inn...· 0 citations
Background: Reliable melanoma classification requires models that capture both local dermoscopic morphology and broader contextual patterns while maintaining auditable, leakageaware internal validation. Objectives: To develop and internally validate an EfficientNetB0-Swin Transformer Tiny ensemble for classifying histo...
The results show that both the CNN architectures used for the experiment and the automated classification of skin lesions using them are effective, and the MobileNetV2 performs the best in the experimental framework of this study.
Raees Adnan, Fawad Nasim, Muqaddas Salahuddin· SOCIAL PRISM· 0 citations
Known for his clear and elegant writing style, Bertsekas shaped fields from control and optimization to large-scale computation and artificial intelligence.