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DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection
Research in the field of medicine and relevant studies evince that melanoma is one of the deadliest cancers. It defines precisely that the condition develops due to uncontrolled growth of melanocytic cells. The current trends in any disease detection revolve around the usage of two main categories o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400005/ https://www.ncbi.nlm.nih.gov/pubmed/36034768 http://dx.doi.org/10.1007/s00500-022-07406-z |
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author | Girdhar, Nancy Sinha, Aparna Gupta, Shivang |
author_facet | Girdhar, Nancy Sinha, Aparna Gupta, Shivang |
author_sort | Girdhar, Nancy |
collection | PubMed |
description | Research in the field of medicine and relevant studies evince that melanoma is one of the deadliest cancers. It defines precisely that the condition develops due to uncontrolled growth of melanocytic cells. The current trends in any disease detection revolve around the usage of two main categories of models; these are general machine learning models and deep learning models. Further, the experimental analysis of melanoma has an additional requirement of visual records like dermatological scans or normal camera lens images. This further accentuates the need for a more accurate model for melanoma detection. In this work, we aim to achieve the same, primarily by the extensive usage of neural networks. Our objective is to propose a deep learning CNN framework-based model to improve the accuracy of melanoma detection by customizing the number of layers in the network architecture, activation functions applied, and the dimension of the input array. Models like Resnet, DenseNet, Inception, and VGG have proved to yield appreciable accuracy in melanoma detection. However, in most cases, the dataset was classified into malignant or benign classes only. The dataset used in our research provides seven lesions; these are melanocytic nevi, melanoma, benign keratosis, basal cell carcinoma, actinic keratoses, vascular lesions, and dermatofibroma. Thus, through the HAM10000 dataset and various deep learning models, we diversified the precision factors as well as input qualities. The obtained results are highly propitious and establish its credibility. |
format | Online Article Text |
id | pubmed-9400005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-94000052022-08-24 DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection Girdhar, Nancy Sinha, Aparna Gupta, Shivang Soft comput Focus Research in the field of medicine and relevant studies evince that melanoma is one of the deadliest cancers. It defines precisely that the condition develops due to uncontrolled growth of melanocytic cells. The current trends in any disease detection revolve around the usage of two main categories of models; these are general machine learning models and deep learning models. Further, the experimental analysis of melanoma has an additional requirement of visual records like dermatological scans or normal camera lens images. This further accentuates the need for a more accurate model for melanoma detection. In this work, we aim to achieve the same, primarily by the extensive usage of neural networks. Our objective is to propose a deep learning CNN framework-based model to improve the accuracy of melanoma detection by customizing the number of layers in the network architecture, activation functions applied, and the dimension of the input array. Models like Resnet, DenseNet, Inception, and VGG have proved to yield appreciable accuracy in melanoma detection. However, in most cases, the dataset was classified into malignant or benign classes only. The dataset used in our research provides seven lesions; these are melanocytic nevi, melanoma, benign keratosis, basal cell carcinoma, actinic keratoses, vascular lesions, and dermatofibroma. Thus, through the HAM10000 dataset and various deep learning models, we diversified the precision factors as well as input qualities. The obtained results are highly propitious and establish its credibility. Springer Berlin Heidelberg 2022-08-24 /pmc/articles/PMC9400005/ /pubmed/36034768 http://dx.doi.org/10.1007/s00500-022-07406-z Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Focus Girdhar, Nancy Sinha, Aparna Gupta, Shivang DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title | DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title_full | DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title_fullStr | DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title_full_unstemmed | DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title_short | DenseNet-II: an improved deep convolutional neural network for melanoma cancer detection |
title_sort | densenet-ii: an improved deep convolutional neural network for melanoma cancer detection |
topic | Focus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400005/ https://www.ncbi.nlm.nih.gov/pubmed/36034768 http://dx.doi.org/10.1007/s00500-022-07406-z |
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