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. 2022 Sep 26:e13141.
doi: 10.1111/exsy.13141. Online ahead of print.

Detection of COVID-19 and its pulmonary stage using Bayesian hyperparameter optimization and deep feature selection methods

Affiliations

Detection of COVID-19 and its pulmonary stage using Bayesian hyperparameter optimization and deep feature selection methods

Nedim Muzoğlu et al. Expert Syst. .

Abstract

Since the first case of COVID-19 was reported in December 2019, many studies have been carried out on artificial intelligence for the rapid diagnosis of the disease to support health services. Therefore, in this study, we present a powerful approach to detect COVID-19 and COVID-19 findings from computed tomography images using pre-trained models using two different datasets. COVID-19, influenza A (H1N1) pneumonia, bacterial pneumonia and healthy lung image classes were used in the first dataset. Consolidation, crazy-paving pattern, ground-glass opacity, ground-glass opacity and consolidation, ground-glass opacity and nodule classes were used in the second dataset. The study consists of four steps. In the first two steps, distinctive features were extracted from the final layers of the pre-trained ShuffleNet, GoogLeNet and MobileNetV2 models trained with the datasets. In the next steps, the most relevant features were selected from the models using the Sine-Cosine optimization algorithm. Then, the hyperparameters of the Support Vector Machines were optimized with the Bayesian optimization algorithm and used to reclassify the feature subset that achieved the highest accuracy in the third step. The overall accuracy obtained for the first and second datasets is 99.46% and 99.82%, respectively. Finally, the performance of the results visualized with Occlusion Sensitivity Maps was compared with Gradient-weighted class activation mapping. The approach proposed in this paper outperformed other methods in detecting COVID-19 from multiclass viral pneumonia. Moreover, detecting the stages of COVID-19 in the lungs was an innovative and successful approach.

Keywords: Bayesian optimization; H1N1 viral pneumonia; bacterial pneumonia; chest CT findings; feature selection; occlusion sensitivity maps; sine–cosine optimization.

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Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

FIGURE 1
FIGURE 1
Percentage distributions of the images. (a) CPBH dataset, and (b) CovCT‐findings dataset
FIGURE 2
FIGURE 2
Computed tomography (CT) images from the CPBH dataset used in the experimental analysis of this study. (a) COVID‐19 pneumonia, (b) H1N1 viral pneumonia, (c) bacterial pneumonia, (d) healthy lung images
FIGURE 3
FIGURE 3
Computed tomography (CT) images of COVID‐19 pulmonary stages from the CovCT‐findings dataset used in the experimental analysis of this study. (a) Crazy‐paving‐pattern (b) consolidation, (c) ground‐glass opacities, (d) ground‐glass opacities and nodule, (e) ground‐glass opacities and consolidation
FIGURE 4
FIGURE 4
Effects of sine and cosine in Equations (7) and (8) on the next position
FIGURE 5
FIGURE 5
Representation of three classes of linear separable multi‐class support vector machines
FIGURE 6
FIGURE 6
Overall block diagram of SCA‐BayeSVMNet multi‐class approach
FIGURE 7
FIGURE 7
Training and validation accuracy graphs of the CPBH dataset with convolutional neural network (CNN) models. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 8
FIGURE 8
Confusion matrix of the pre‐trained models using Softmax on CPBH dataset. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 9
FIGURE 9
Confusion matrix of the pre‐trained models using support vector machine (SVM) on CPBH dataset. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 10
FIGURE 10
Confusion matrix of the pre‐trained models using support vector machine (SVM) and sine‐cosine algorithm (SCA) method on CPBH dataset. (a) GoogLeNet, (b) MobileNetV2, (c) ShuffleNet, (d) combined 515 features and (e) 5‐fold cross validation for combined 515 features
FIGURE 11
FIGURE 11
(a) Min classification error graph using Bayesian optimization algorithm with combined 515 features, (b) best point hyperparameter optimization confusion matrix of 515 combined features
FIGURE 12
FIGURE 12
Training and validation accuracy graphs of the CovCT‐findings dataset with convolutional neural network (CNN) models. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 13
FIGURE 13
Confusion matrix of the pre‐trained models using Softmax on CovCT‐findings dataset. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 14
FIGURE 14
Confusion matrix of the pre‐trained models using support vector machine (SVM) on CovCT‐findings dataset. (a) GoogLeNet, (b) MobileNetV2 and (c) ShuffleNet
FIGURE 15
FIGURE 15
Confusion matrices from classification of CovCT‐findings dataset using the sine‐cosine algorithm (SCA) method. (a) GoogLeNet, (b) MobileNetV2, (c) ShuffleNet, (d) combined 683 features, (e) 5‐fold cross validation for combined 683 features
FIGURE 16
FIGURE 16
(a) Min classification error graph using Bayesian optimization algorithm with combined 683 features, (b) best point hyperparameter optimization confusion matrix of 683 combined features
FIGURE 17
FIGURE 17
Comparison of occlusion sensitivity maps and grad‐CAM in differentiating multifocal lesions in COVID‐19 and CovCT findings classes. (a) Ground‐glass opacities, (b) ground‐glass opacities and nodule (c) crazy‐paving‐pattern (d) consolidation, (e) bacterial pneumonia (f) H1N1 viral pneumonia, (g) healthy lung

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