ArticleDiagnostics (Basel, Switzerland)2023
Assist-Dermo: A Lightweight Separable Vision Transformer Model for Multiclass Skin Lesion Classification.
Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 25 citations in OpenAlex.
- Quantum-enhanced multimodal prognostic transformer for skin disease progression prediction and visualization.Scientific reports · 2026Article
- Explainable depth-wise and channel-wise fusion models for multi-class skin lesion classification.PloS one · 2026Article
- LBNet: an optimized lightweight CNN for mammographic breast cancer classification with XAI-based interpretability.Scientific reports · 2025Article
- Explainable AI-Based Skin Cancer Detection Using CNN, Particle Swarm Optimization and Machine Learning.Journal of imaging · 2024Article
- A novel Skin lesion prediction and classification technique: ViT-GradCAM.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024Article
- Skin Cancer Detection and Classification Using Neural Network Algorithms: A Systematic Review.Diagnostics (Basel, Switzerland) · 2024Review
- AI in dermatology: a comprehensive review into skin cancer detection.PeerJ. Computer science · 2024Article
- An ensemble-based deep learning model for detection of mutation causing cutaneous melanoma.Scientific reports · 2023Article
- Dermo-Seg: ResNet-UNet Architecture and Hybrid Loss Function for Detection of Differential Patterns to Diagnose Pigmented Skin Lesions.Diagnostics (Basel, Switzerland) · 2023Article
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 3 countries.
Funding
Abstract
A dermatologist-like automatic classification system is developed in this paper to recognize nine different classes of pigmented skin lesions (PSLs), using a separable vision transformer (SVT) technique to assist clinical experts in early skin cancer detection. In the past, researchers have developed a few systems to recognize nine classes of PSLs. However, they often require enormous computations to achieve high performance, which is burdensome to deploy on resource-constrained devices. In this paper, a new approach to designing SVT architecture is developed based on SqueezeNet and depthwise separable CNN models. The primary goal is to find a deep learning architecture with few parameters that has comparable accuracy to state-of-the-art (SOTA) architectures. This paper modifies the SqueezeNet design for improved runtime performance by utilizing depthwise separable convolutions rather than simple conventional units. To develop this Assist-Dermo system, a data augmentation technique is applied to control the PSL imbalance problem. Next, a pre-processing step is integrated to select the most dominant region and then enhance the lesion patterns in a perceptual-oriented color space. Afterwards, the Assist-Dermo system is designed to improve efficacy and performance with several layers and multiple filter sizes but fewer filters and parameters. For the training and evaluation of Assist-Dermo models, a set of PSL images is collected from different online data sources such as Ph2, ISBI-2017, HAM10000, and ISIC to recognize nine classes of PSLs. On the chosen dataset, it achieves an accuracy (ACC) of 95.6%, a sensitivity (SE) of 96.7%, a specificity (SP) of 95%, and an area under the curve (AUC) of 0.95. The experimental results show that the suggested Assist-Dermo technique outperformed SOTA algorithms when recognizing nine classes of PSLs. The Assist-Dermo system performed better than other competitive systems and can support dermatologists in the diagnosis of a wide variety of PSLs through dermoscopy. The Assist-Dermo model code is freely available on GitHub for the scientific community.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.