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Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet

Skin lesions are one of the typical symptoms of many diseases in humans and indicative of many types of cancer worldwide. Increased risks caused by the effects of climate change and a high cost of treatment, highlight the importance of skin cancer prevention efforts like this. The methods used to de...

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Autores principales: Cano, Elia, Mendoza-Avilés, José, Areiza, Mariana, Guerra, Noemi, Mendoza-Valdés, José Longino, Rovetto, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189026/
https://www.ncbi.nlm.nih.gov/pubmed/34150994
http://dx.doi.org/10.7717/peerj-cs.371
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author Cano, Elia
Mendoza-Avilés, José
Areiza, Mariana
Guerra, Noemi
Mendoza-Valdés, José Longino
Rovetto, Carlos A.
author_facet Cano, Elia
Mendoza-Avilés, José
Areiza, Mariana
Guerra, Noemi
Mendoza-Valdés, José Longino
Rovetto, Carlos A.
author_sort Cano, Elia
collection PubMed
description Skin lesions are one of the typical symptoms of many diseases in humans and indicative of many types of cancer worldwide. Increased risks caused by the effects of climate change and a high cost of treatment, highlight the importance of skin cancer prevention efforts like this. The methods used to detect these diseases vary from a visual inspection performed by dermatologists to computational methods, and the latter has widely used automatic image classification applying Convolutional Neural Networks (CNNs) in medical image analysis in the last few years. This article presents an approach that uses CNNs with a NASNet architecture to recognize in a more accurate way, without segmentation, eight skin diseases. The model was trained end-to-end on Keras with augmented skin diseases images from the International Skin Imaging Collaboration (ISIC). The CNN architectures were initialized with weight from ImageNet, fine-tuned in order to discriminate well among the different types of skin lesions, and then 10-fold cross-validation was applied. Finally, some evaluation metrics are calculated as accuracy, sensitivity, and specificity and compare with other CNN trained architectures. This comparison shows that the proposed system offers higher accuracy results, with a significant reduction on the training paraments. To the best of our knowledge and based in the state-of-art recompiling in this work, the application of the NASNet architecture training with skin image lesion from ISIC archive for multi-class classification and evaluated by cross-validation, represents a novel skin disease classification system.
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spelling pubmed-81890262021-06-17 Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet Cano, Elia Mendoza-Avilés, José Areiza, Mariana Guerra, Noemi Mendoza-Valdés, José Longino Rovetto, Carlos A. PeerJ Comput Sci Bioinformatics Skin lesions are one of the typical symptoms of many diseases in humans and indicative of many types of cancer worldwide. Increased risks caused by the effects of climate change and a high cost of treatment, highlight the importance of skin cancer prevention efforts like this. The methods used to detect these diseases vary from a visual inspection performed by dermatologists to computational methods, and the latter has widely used automatic image classification applying Convolutional Neural Networks (CNNs) in medical image analysis in the last few years. This article presents an approach that uses CNNs with a NASNet architecture to recognize in a more accurate way, without segmentation, eight skin diseases. The model was trained end-to-end on Keras with augmented skin diseases images from the International Skin Imaging Collaboration (ISIC). The CNN architectures were initialized with weight from ImageNet, fine-tuned in order to discriminate well among the different types of skin lesions, and then 10-fold cross-validation was applied. Finally, some evaluation metrics are calculated as accuracy, sensitivity, and specificity and compare with other CNN trained architectures. This comparison shows that the proposed system offers higher accuracy results, with a significant reduction on the training paraments. To the best of our knowledge and based in the state-of-art recompiling in this work, the application of the NASNet architecture training with skin image lesion from ISIC archive for multi-class classification and evaluated by cross-validation, represents a novel skin disease classification system. PeerJ Inc. 2021-06-03 /pmc/articles/PMC8189026/ /pubmed/34150994 http://dx.doi.org/10.7717/peerj-cs.371 Text en © 2021 Cano et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Computer Science) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Cano, Elia
Mendoza-Avilés, José
Areiza, Mariana
Guerra, Noemi
Mendoza-Valdés, José Longino
Rovetto, Carlos A.
Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title_full Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title_fullStr Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title_full_unstemmed Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title_short Multi skin lesions classification using fine-tuning and data-augmentation applying NASNet
title_sort multi skin lesions classification using fine-tuning and data-augmentation applying nasnet
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189026/
https://www.ncbi.nlm.nih.gov/pubmed/34150994
http://dx.doi.org/10.7717/peerj-cs.371
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