Enhancing breast cancer diagnosis using deep learning and gradient multi-verse optimizer: a robust biomedical data analysis approach

Breast cancer (BC) is one of the most common causes of mortality among women. However, early detection of BC can effectively improve the treatment outcomes. Computer-aided diagnosis (CAD) systems can be utilized clinical specialists for accurate diagnosis of BC in its early stages. Due to their superior classification performance, deep learning (DL) methods have been extensively used in CAD systems. The classification accuracy of a DL model mainly depends on the parameters, such as weights and biases, of the deep neural network (DNN), which are optimized during the training phase. The training of DL models has been carried out by gradient-based techniques, <i>e.g</i>., stochastic gradient descent with momentum (SGDM) and adaptive momentum estimation (ADAM), and metaheuristic techniques, <i>e.g</i>., genetic algorithms (GA) and particle swarm optimization (PSO). However, these techniques suffer from frequent stagnation in local optima due to the huge search space, which can lead to sub-optimal DL performance. This article proposes a hybrid optimization algorithm, based on incorporating a simple gradient search mechanism into a metaheuristic technique, multi-verse optimizer (MVO), to facilitate the search for global optimal solution in the high-dimensional search space of DL models. A DL model for BC diagnosis is developed based on a three-hidden-layer DNN whose parameters are optimized using the proposed hybrid optimizer. Experimental analysis is carried out on the Wisconsin breast cancer dataset (WBCD) and the Wisconsin Diagnosis Breast Cancer (WDBC) dataset, each is divided into 70% for training and 30% for testing. For comparison reasons, similar DL models trained using various optimizers, including gradient-based, metaheuristic, and recently-proposed hybrid optimization algorithms, are also analyzed. The results demonstrate the superior performance of our optimizer in terms of attaining the most accurate DL model in the fastest convergence rate. The proposed model achieves outstanding metrics, including accuracy at 93.5%, precision at 88.06%, specificity at 93.06%, sensitivity at 95.64%, F1 score at 91.67%, and Matthew's correlation coefficient (MCC) at 87.14% on WBCD, and accuracy at 96.73%, precision at 93.38%, specificity at 95.83%, sensitivity at 98.25%, F1 score at 95.75%, and MCC at 93.18% on WDBC, in just six epochs. This research significantly contributes to advancing CAD systems for BC, emphasizing the potential benefits of the proposed optimizer in medical classification domains.

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Publication Details

Journal
PeerJ Computer Science
Published
2024-12-23
DOI
https://doi.org/10.7717/peerj-cs.2578
Citations
2
Primary Topic
Spectroscopy and Chemometric Analyses
Type
article
Field-Weighted Citation Impact
0.47

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article

Enhancing breast cancer diagnosis using deep learning and gradient multi-verse optimizer: a robust biomedical data analysis approach

Talal Ahmed Ali Ali, Mundher Mohammed Taresh, Yassine EL Kati, Shulin Wang
2 citations
PeerJ Computer Science
Spectroscopy and Chemometric Analyses
0.47
article

Enhancing breast cancer diagnosis using deep learning and gradient multi-verse optimizer: a robust biomedical data analysis approach

Talal Ahmed Ali Ali, Mundher Mohammed Taresh, Yassine EL Kati, Shulin Wang
article en
2 citations

Abstract

Breast cancer (BC) is one of the most common causes of mortality among women. However, early detection of BC can effectively improve the treatment outcomes. Computer-aided diagnosis (CAD) systems can be utilized clinical specialists for accurate diagnosis of BC in its early stages. Due to their superior classification performance, deep learning (DL) methods have been extensively used in CAD systems. The classification accuracy of a DL model mainly depends on the parameters, such as weights and biases, of the deep neural network (DNN), which are optimized during the training phase. The training of DL models has been carried out by gradient-based techniques, <i>e.g</i>., stochastic gradient descent with momentum (SGDM) and adaptive momentum estimation (ADAM), and metaheuristic techniques, <i>e.g</i>., genetic algorithms (GA) and particle swarm optimization (PSO). However, these techniques suffer from frequent stagnation in local optima due to the huge search space, which can lead to sub-optimal DL performance. This article proposes a hybrid optimization algorithm, based on incorporating a simple gradient search mechanism into a metaheuristic technique, multi-verse optimizer (MVO), to facilitate the search for global optimal solution in the high-dimensional search space of DL models. A DL model for BC diagnosis is developed based on a three-hidden-layer DNN whose parameters are optimized using the proposed hybrid optimizer. Experimental analysis is carried out on the Wisconsin breast cancer dataset (WBCD) and the Wisconsin Diagnosis Breast Cancer (WDBC) dataset, each is divided into 70% for training and 30% for testing. For comparison reasons, similar DL models trained using various optimizers, including gradient-based, metaheuristic, and recently-proposed hybrid optimization algorithms, are also analyzed. The results demonstrate the superior performance of our optimizer in terms of attaining the most accurate DL model in the fastest convergence rate. The proposed model achieves outstanding metrics, including accuracy at 93.5%, precision at 88.06%, specificity at 93.06%, sensitivity at 95.64%, F1 score at 91.67%, and Matthew's correlation coefficient (MCC) at 87.14% on WBCD, and accuracy at 96.73%, precision at 93.38%, specificity at 95.83%, sensitivity at 98.25%, F1 score at 95.75%, and MCC at 93.18% on WDBC, in just six epochs. This research significantly contributes to advancing CAD systems for BC, emphasizing the potential benefits of the proposed optimizer in medical classification domains.

PeerJ Computer ScienceVol. 10
Hunan University (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 39%
Spectroscopy and Chemometric Analyses
0.47
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