Data, Depth, and Design: Learning Reliable Models for Skin Lesion Analysis
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Abstract (arXiv)
Deep learning fostered a leap ahead in automated skin lesion analysis in the last two years. Those models are expensive to train and difficult to parameterize. Objective: We investigate methodological issues for designing and evaluating deep learning models for skin lesion analysis. We explore 10 choices faced by researchers: use of transfer learning, model architecture, train dataset, image resolution, type of data augmentation, input normalization, use of segmentation, duration of training, additional use of SVMs, and test data augmentation. Methods: We perform two full factorial experiments, for five different test datasets, resulting in 2560 exhaustive trials in our main experiment, and 1280 trials in our assessment of transfer learning. We analyze both with multi-way ANOVA. We use the exhaustive trials to simulate sequential decisions and ensembles, with and without the use of privileged information from the test set. Results -- main experiment: Amount of train data has disproportionate influence, explaining almost half the variation in performance. Of the other factors, test data augmentation and input resolution are the most influential. Deeper models, when combined, with extra data, also help. -- transfer experiment: Transfer learning is critical, its absence brings huge performance penalties. -- simulations: Ensembles of models are the best option to provide reliable results with limited resources, without using privileged information and sacrificing methodological rigor. Conclusions and Significance: Advancing research on automated skin lesion analysis requires curating larger public datasets. Indirect use of privileged information from the test set to design the models is a subtle, but frequent methodological mistake that leads to overoptimistic results. Ensembles of models are a cost-effective alternative to the expensive full-factorial and to the unstable sequential designs.
Key facts. Cited by 8 papers in the map (data through 7 Oct 2026). First posted on arXiv 1 Nov 2017.
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Citing papers per year: 2021: 4; 2022: 1; 2023: 1; 2024: 1; 2025: 0; 2026: 1.
8 papers.
- 2021GAN-Based Data Augmentation and Anonymization for Skin-Lesion Analysis: A Critical Reviewcited by 25
- 2022A Survey on Deep Learning for Skin Lesion Segmentationcited by 22
- 2021Soft-Attention Improves Skin Cancer Classification Performancecited by 15
- 2021An Evaluation of Self-Supervised Pre-Training for Skin-Lesion Analysiscited by 10
- 2021Dermo-DOCTOR: A framework for concurrent skin lesion detection and recognition using a deep convolutional neural network with end-to-end dual encoderscited by 4
- 2023Assessing the Generalizability of Deep Neural Networks-Based Models for Black Skin Lesionscited by 3
- 2024Are Explanations Helpful? A Comparative Analysis of Explainability Methods in Skin Lesion Classifierscited by 0
- 2026Searching for Robust Augmentations to Improve Out-of-Domain Generalization in Dermoscopic Skin Cancer Classificationcited by 0
- 2026Searching for Robust Augmentations to Improve Out-of-Domain Generalization in Dermoscopic Skin Cancer Classification29 Jul 2026
- 2024Are Explanations Helpful? A Comparative Analysis of Explainability Methods in Skin Lesion Classifiers4 Dec 2024
- 2023Assessing the Generalizability of Deep Neural Networks-Based Models for Black Skin Lesions30 Sep 2023
- 2022A Survey on Deep Learning for Skin Lesion Segmentation1 Jun 2022
- 2021An Evaluation of Self-Supervised Pre-Training for Skin-Lesion Analysis17 Jun 2021
- 2021Soft-Attention Improves Skin Cancer Classification Performance5 May 2021
- 2021GAN-Based Data Augmentation and Anonymization for Skin-Lesion Analysis: A Critical Review20 Apr 2021
- 2021Dermo-DOCTOR: A framework for concurrent skin lesion detection and recognition using a deep convolutional neural network with end-to-end dual encoders3 Feb 2021