Relative likelihood based aggregated dual deep neural network for skin lesion recognition in dermoscopy images
This paper presents a novel approach classifying benign and malignant skin lesions based on dermoscopy images using a deep learning (DL) framework. We present a dual deep neural network (DDNN) to solve the problem of classification accuracy (ACC) that varies from class to class, which happens when d...
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Published in: | Multimedia tools and applications Vol. 83; no. 21; pp. 60603 - 60626 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
New York
Springer US
2024
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | This paper presents a novel approach classifying benign and malignant skin lesions based on dermoscopy images using a deep learning (DL) framework. We present a dual deep neural network (DDNN) to solve the problem of classification accuracy (ACC) that varies from class to class, which happens when different feature sets work better for different classes. This DDNN comprises two deep neural networks (DNN) designed to extract and characterize lesions, utilizing two distinct handcrafted feature sets: phase congruency features and (PC) Gabor features (GA). PC is known for its resilience to illumination and contrast variations, and GA captures high-frequency directional information in localized regions surrounding the lesion. The DDNN outputs of these two-trained networks are aggregated, employing a novel likelihood-based add-and-compare decision (LACD) in the output layer. With the utilization of training data, this proposed method generates additional discriminative features that aid in the classification of malignant and benign. To evaluate the effectiveness of our approach, ablation studies and experiments were conducted using skin cancer images from the ISIC archive, achieving a normalised ACC of 87.76% for ISIC2016 and 84.25% for ISIC2017. The performance of our method is also compared with existing skin lesion classification methods. |
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ISSN: | 1573-7721 1380-7501 1573-7721 |
DOI: | 10.1007/s11042-023-17908-z |