
Bone cancer detection is an essential region of medical analysis but developments in medical imaging and artificial intelligence (AI) are vital. Using approaches, namely deep learning (DL) and machine learning (ML), radiologists and medical staff can examine X-ray, CT, and MRI scans to identify bone cancer and abnormalities. These technologies support earlier diagnosis, correct diagnosis, and treatment planning, enhancing patient solutions. The combination of AI-driven image analysis and the knowledge of medical practitioners improves the speed and precision of bone cancer detection, contributing to more effectual clinical activities. DL algorithms, particularly CNNs, are exposed to great performance in image classification tasks and are extremely utilized for medical image analysis. We offer a Hybrid Rice Optimization Algorithm with DL-Assisted Bone Cancer Detection (HROADL-BCD) technique on medical X-ray images. The major intention of the HROADL-BCD method is to examine the X-ray images for the recognition of bone cancer. In the presented HROADL-BCD method, a bilateral filtering (BF) process was performed to remove the noise. To derive feature vectors, the HROADL-BCD technique applied the EfficientNet model. The HROADL-BCD technique involved the HROA for hyperparameter tuning of the EfficientNet model. Last, the bone cancer detection and classification process were executed by the attention-based bidirectional long short-term memory (ABiLSTM) approach. A wide range of simulations could be applied for the simulation result analysis of the HROADL-BCD algorithm. The extensive outcome of the HROADL-BCD approach inferred the superior outcome of 97.62% outcome concerning various aspects.
Citation: Thavavel Vaiyapuri, Prasanalakshmi Balaji, S. Shridevi, Santhi Muttipoll Dharmarajlu, Nourah Ali AlAseem. An attention-based bidirectional long short-term memory based optimal deep learning technique for bone cancer detection and classifications[J]. AIMS Mathematics, 2024, 9(6): 16704-16720. doi: 10.3934/math.2024810
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Bone cancer detection is an essential region of medical analysis but developments in medical imaging and artificial intelligence (AI) are vital. Using approaches, namely deep learning (DL) and machine learning (ML), radiologists and medical staff can examine X-ray, CT, and MRI scans to identify bone cancer and abnormalities. These technologies support earlier diagnosis, correct diagnosis, and treatment planning, enhancing patient solutions. The combination of AI-driven image analysis and the knowledge of medical practitioners improves the speed and precision of bone cancer detection, contributing to more effectual clinical activities. DL algorithms, particularly CNNs, are exposed to great performance in image classification tasks and are extremely utilized for medical image analysis. We offer a Hybrid Rice Optimization Algorithm with DL-Assisted Bone Cancer Detection (HROADL-BCD) technique on medical X-ray images. The major intention of the HROADL-BCD method is to examine the X-ray images for the recognition of bone cancer. In the presented HROADL-BCD method, a bilateral filtering (BF) process was performed to remove the noise. To derive feature vectors, the HROADL-BCD technique applied the EfficientNet model. The HROADL-BCD technique involved the HROA for hyperparameter tuning of the EfficientNet model. Last, the bone cancer detection and classification process were executed by the attention-based bidirectional long short-term memory (ABiLSTM) approach. A wide range of simulations could be applied for the simulation result analysis of the HROADL-BCD algorithm. The extensive outcome of the HROADL-BCD approach inferred the superior outcome of 97.62% outcome concerning various aspects.
Bone cancer arises from strong cells and then initiates cancer. The initial sign of bone tumor is bone cancer. The cancer develops steadily and can extend to different body parts [1]. It can ruin the bone tissues and then make the bone fragile. According to the data, 3,500 persons in the USA were afflicted with bone cancer in 2018. Approximately 47 percent of people with bone cancer perish. Through many tests, the surgeon analyzes the tumors. The X-ray radiograph analysis is utilized to identify tumors in the bones of humanoids. The strong bone and the tumorous bone X-ray integration rates are dissimilar [2]. Because of that, a tumorous bone image surface seems shabby. The bone cancer harshness is dignified by a phase and the status. Tumor progress level is employed by physicians to forecast the illness progress ratio [3]. Analyzing tumors in the bone needs proficiency. A physician does bone cancer analyses physically; therefore, it is time-consuming, and there is a chance of a mistake.
Initial recognition appears to be the mere factor that enhances the likelihood of being tumor-infected victims [4]. The analysis of bone cancer is established through 3 features: Histopathologic aspect, imaging, and symptomatology. Unluckily, the signs are nonspecific, and they deliver slight information to direct the analysis to two major types of bone tumors, mainly in the initial phases of the illness [5]. The histopathologic analysis is the crucial component, which offers the utmost precise analysis and begins the therapeutic method. Assuming its aggressive nature, this analysis characterizes the concluding phase of the analytical procedure. For the highest precision, imaging information is essential to define the utmost suitable region for harvesting [6]. Because of the modern key technical improvements, imaging examinations have grown increasingly successful.
ML and AI have made rapid progress in recent times [7]. The utilization of AI and ML techniques has significantly contributed to the advancement in medical domains such as image interpretation, image registration, Image-guided therapy, medical image processing, image fusion, and image segmentation. These methods have been proven to extract and represent information from medical images in a highly effective and efficient manner. AI and ML enable and support medics so that they can analyze and forecast precise and earlier threats of illnesses and stop them [8]. These methods improve the capabilities of medics and scientists to recognize how to examine the common differences that will give rise to the illness. Though automatic recognition of illnesses depends on conservative approaches in therapeutic imaging and has been exposed to important precisions for years, novel improvements in ML methods have exploded in the DL [9]. DL-dependent procedures exhibit encouraging presentation in various fields such as drug detection, lips reading, computer-aided analysis, text identification, speech identification, lip reading, computer-aided analysis, and face identification [10].
We offer a Hybrid Rice Optimization Algorithm with DL-Assisted Bone Cancer Detection (HROADL-BCD) technique on medical X-ray images. In the presented HROADL-BCD technique, a bilateral filtering (BF) process is performed to remove the noise. To derive feature vectors, the HROADL-BCD technique applies the EfficientNet model. The HROADL-BCD technique involves the HROA for hyperparameter tuning of the EfficientNet model. Last, the bone cancer detection and classification process were applied by an attention-based bidirectional long short-term memory (ABiLSTM) system. For simulation result analysis of the HROADL-BCD algorithm, a wide range of simulations can be executed.
Rehman et al. [11] designed for a tool for diagnosing osteoarthritis. The recent DL-based CNN and numerous ML-based algorithms have been implemented for evaluation. A new TL-based feature engineering method CRK (CNN, RF, and KNN) was developed. By employing a 2D-CNN, the CRK rapidly removes the spatial features that could be transferred to the RF and KNN methods, producing probabilistic feature sets. In [12], the Seg-Unet framework with patched and global-based techniques is introduced. This technique includes higher-risk area segmentation, cancer segmentation, and classification subdivisions for learning collective advantages between the local textures at all pixels and the global context of the whole image. The patch-based algorithm increases effectiveness in malignant tumor identification.
Bharodiya and Gonsai [13] projected an intelligent assistive method named BTDBB. This developed method takes human arm X-ray images, improves to split images into various sections depending on crop image to maintain only ROI, transforms into grayscale, performs Gaussian filtering (GF) for eliminating noise and segmentation, identification of ROI employing binary blob pattern analyses, diagnosing bone cancer, threshold, and determination of cancer size. Xu et al. [14] introduced a novel necrosis rate identification technique utilizing time series X-ray images. This presented technique employs a GAN with LSTM for producing time series X-ray images. An image-to-image transferred network was implemented to generate the major images for more data extension. This data augmentation has been referred to as a training set of 3D-CNN classification techniques.
Wani and Arora [15] projected a CNN-based technique. The TL of DL-based CNNs such as VggNet19, AlexNet, ResNet, and VggNet16 could be employed for categorizing the X-ray images. Our major aims are: To introduce a database of 381 knee x-rays pathologically confirmed by the T-scores acquired in the Quantitative Ultrasound technique, and to develop a DL algorithm employing TL for classification. Singh et al. [16] suggested an innovative method for diagnosing bone cancer that depends on classification and feature extraction employing the DL approach. After preprocessing, the features are removed by exploiting ROI extraction and Convolution HOG gradients (CHOG) technique. To classify the correct spotting and grading of the bone tissue as abnormal and normal, the presented model utilized the extreme Convolutional DL machine (ECDLM) approach.
In [17], a multi-feature aggregation block called a combined gate was presented. This developed combined gate is to make a regenerated feature, which includes both higher-level and lower-level data. Therefore, the regenerated feature was integrated with the smaller scare feature cued with a local feature fusion algorithm, attaining multi-scare feature aggregation. Moreover, an innovative X-ray image database has been developed for segmenting bone cancers. Gül et al. [18] implemented an innovative DL-based technique for automatically detecting pes planus through X-ray images. A novel pes planus database was employed. Followed by preprocessing, the images are provided to the pre-training MobileNetV2, and features are removed in the Logits layer.
In this manuscript, an automated bone cancer detection method known as the HROADL-BCD technique on X-ray images is presented. The major intention of the HROADL-BCD technique is to inspect the X-ray images for the recognition of bone cancer. In the proposed HROADL-BCD method, dissimilar phases of operations are BF-based noise removal, EfficientNet feature extraction, ABiLSTM-based classification, and HROA-based hyperparameter tuning. Figure 1 depicts the working process of the HROADL-BCD method.
The BF approach is used to eliminate the noise in the X-ray images. In X-ray imaging, noise, including speckle and Gaussian noise, poses a crucial threat, complicating critical anatomical details and hindering precise diagnosis. Hence, the BF model is significant in mitigating these problems, selectively mitigating noise while safeguarding needful image features and sharp transitions. BF is a great image processing system to efficiently improve and denoise images by maintaining boundaries and fine parts [19]. It accomplishes this by assuming either spatial proximity pixel intensity or color similarity once executing a weighted average filtering to adjacent pixels. This method permits BF for smoothing areas with the same preserving sharp transitions, making it a useful tool in distinct image processing applications comprising tone mapping, edge-preserving smoothing, and image denoising, but preserving image fidelity and infrastructure is essential for high-quality performances.
To generate features, the EfficientNet model is applied. EfficientNet is a ground-breaking family of CNN designs, which has caused a major control on the domain of computer vision (CV) [20]. Established by Google's researchers, EfficientNet is known for accomplishing an impressive balance between computational performance and accuracy, making it extremely sought-after for extracting features in distinct image processing and CV tasks. At the center, EfficientNet establishes a new method for scaling the model design, suggested as compound scaling. This method entails scaling the width, resolution, and depth of NN. As a result, EfficientNet optimizes its solution, making sure that as the model dimension enhances, its capability to capture intricate designs and representations is also enhanced. This outcome in methods could not only be extremely effectual but also remarkably correct, making it ideal for extracting features from the application ranges. The compound scaling in EfficientNet is directed by a scaling coefficient, signified as "phi" (ϕ), which handles the model's dimensional and capacity. As ϕ enhances, the model becomes greater and more important. Figure 2 portrays the infrastructure of EfficientNet.
The EfficientNet base structure, called EfficientNetB0, was planned with a certain balance of depth, width (i.e., the count of channels from all the layers), and image resolution. It further involves the MobileNetV2 structure that is recognized for its lightweight design, creating it an effective optimal for computation. EfficientNet establishes scaling factors for depth, width, and resolution, expressed as , , and , correspondingly. These factors define that several dimensions of networks can be scaled once is enhanced. This scaling approach makes sure that higher methods preserve similar comparative proportions as their lesser counterparts, maintaining structural integrity. EfficientNet provides a range of model variations, implied as B0-B7, with a distinct ϕ value. The B0 difference is the minimum and more computationally effective, but B7 is the maximum and most important. This scalability permits practitioners to select the model differently to be suited for its computational resources and performance requirements. Lesser variants are ideal for utilization in resource-constrained environments, but higher variants offer existing solutions for an extensive array of image detection tasks.
In this work, the HROA was executed for the hyperparameter selection of the EfficientNet model. Ye et al. proposed that HRO is a state-of-the-art metaheuristic approach stimulated by the advantages of heterosis, which offers robust global search capabilities and superior search efficiency [21]. Based on their fitness values, HRO splits the population into three lines. Consider as the population is arranged by fitness value, but the population size is represented as . The initial sub-population defined by possesses the best fitness, and constitutes a maintainer line. The second sub-population denoting the poor fitness value from the population is known as the sterile line and it is indicated as , which needs hybridization with the maintainer line to better their fitness quality. The restorer line is the residual sub-population, represented by . Through the selfing process, it evolves into the maintainer line. In the following section, the basic principles of HRO are further discussed.
The hybridization procedure includes crossing the maintainer and sterile lines that possess major differences in their fitness values. By replacing original individuals with new hybrid individuals, the sterile line can be updated if it shows better fitness. Using Eq. (1), the newly generated individuals within the sterile line can be attained:
(1) |
where and are the genes of random individuals chosen from the sterile and maintainer lines. is a random integer within the interval of [0, 1]. refers to the gene of hybrid individuals of the sterile line at iterations.
Selfing
This process is used for updating the restorer line, to steer the individuals toward the best global solution. Such behaviors are mathematically modeled as follows:
(2) |
In Eq (2), , a new gene generated by selfing between and restorer is . signifies the gene of the restorer selected arbitrarily in the restorer line and denotes the gene of the best individual obtained. The parameter is a randomly generated number from [0, 1].
The original candidate solution was evaluated and compared after the generation of the newest individual through hybridization and selfing. As defined in Eq (3), the substitution process is used to replace the old individuals with newer ones as long as the fitness values of a new individual exceed the old one.
(3) |
The selfing procedure in HRO includes tracking the iteration number while the restorer cannot endure upgrades utilizing self‐crossing parameters (SC). When the restorer's SC obtains the upper boundary, represented as iteration without upgrades, then the reset operation can be implemented for that individual. The mathematical modeling of a reset behavior is given below:
(4) |
In Eq (4), shows that the gene of restorer that has not been upgraded, and the maximal and minimal values of dimension are and correspondingly. refers to the random value ranging from zero and one. Note that the performance attained by HRO is continuous and should be mapped into the solution space of FS using the transfer function applications. The sigmoid function is used as a binary map that can be described as follows:
(5) |
(6) |
The HRO algorithm progresses a fitness function (FF) to achieve an enhanced classifier solution. It is used to express the positive integer to state the good efficiency of candidate performance. Here, the decreasing classifier errors are assumed as FF, as depicted in Eq (7).
(7) |
The HROADL-BCD model has been applied to the ABiLSTM model for the image classification process. The LSTM-NN is developed, which relies on RNN for resolving the disappearing and explosion gradient problems [22]. LSTM could capture the standard features of the input dataset. The above problems are efficiently evaded as a parameter of each structure as independent. The internal structure of LSTM is made up of a memory cell an input gate , forget gate , output gate , and existing output . The output values of prior unit , the cell layer of prior unit , and the input database are exploited as input for existing units. Using the following formula, LSTM is defined:
(8) |
(9) |
(10) |
(11) |
(12) |
(13) |
where indicates the Hadamard product, , and are the weighted matrices, , and are bias vectors, and and denote the activation functions. The formula is given below:
(14) |
(15) |
(16) |
In Eq (16), is the bias vector, and is the weight matrix.
Accordingly, Graves and Schmidhuber introduced Bi-LSTM that fuses forward and reverse LSTM. It has more benefits in terms of prediction since it extracts time series data. is provided as the reverse and forward LSTM to attain the output of LSTM. The predicted values can be evaluated by Eq (17):
(17) |
here, and imply the output results of forward as well as reverse LSTM. and denote the weighted matrices and is a bias vector.
There are some differences in the importance of time series features. Based on the CNN and BiLSTM, we present an attention model for assigning weight to the element in the feature sequence. The attention model highlights relevant features, decreases the impact of weakly related features, and assists the model in making more accurate evaluations as follows:
(18) |
In Eq (18), the feature sequence input to the layer of the attention module is , and the weighted sum of weight.
In this study, the experimental outcome of the HROADL-BCD approach is tested on a dataset [23], including 200 samples and 2 classes as denoted in Table 1.
Class Name | No. of Instances |
Cancerous | 100 |
Healthy | 100 |
Total No. of Instances | 200 |
The confusion matrices offered by the HROADL-BCD technique on 70:30 and 80:20 of the TRPH/TSPH are illustrated in Figure 3. The outcome indicates the effective recognition of the healthy and cancerous samples under each 2 class labels.
The bone cancer detection outcomes of the HROADL-BCD technique are examined on 80:20 of the TRPH/TSPH as shown in Table 2 and Figure 4. The simulated outcomes pointed out that the HROADL-BCD method proficiently classifies every 2 samples. Moreover, based on 80% of the TRPH, the HROADL-BCD technique obtains average , , , , , and values of 93.75%, 93.75%, 93.75%, 93.75%, 87.50%, and 93.75% respectively. Likewise, with 20% of the TSPH, the HROADL-BCD system attains average , , , , , and values of 97.62%, 97.50%, 97.62%, 97.50%, 95.12%, and 97.53%, respectively.
Class | MCC | G-Measure | ||||
TRPH (80%) | ||||||
Cancerous | 93.67 | 93.67 | 93.67 | 93.67 | 87.50 | 93.67 |
Healthy | 93.83 | 93.83 | 93.83 | 93.83 | 87.50 | 93.83 |
Average | 93.75 | 93.75 | 93.75 | 93.75 | 87.50 | 93.75 |
TSPH (20%) | ||||||
Cancerous | 95.24 | 100.00 | 95.24 | 97.56 | 95.12 | 97.59 |
Healthy | 100.00 | 95.00 | 100.00 | 97.44 | 95.12 | 97.47 |
Average | 97.62 | 97.50 | 97.62 | 97.50 | 95.12 | 97.53 |
The bone cancer detection examination of the HROADL-BCD method can be investigated at 70:30 of the TRPH/TSPH as shown in Table 3 and Figure 5. The simulated outcomes denote that the HROADL-BCD system categorizes 2 samples efficiently.
Class | MCC | G-Measure | ||||
TRPH (70%) | ||||||
Cancerous | 93.06 | 95.71 | 93.06 | 94.37 | 88.61 | 94.38 |
Healthy | 95.59 | 92.86 | 95.59 | 94.20 | 88.61 | 94.21 |
Average | 94.32 | 94.29 | 94.32 | 94.28 | 88.61 | 94.29 |
TSPH (30%) | ||||||
Cancerous | 96.43 | 96.43 | 96.43 | 96.43 | 93.30 | 96.43 |
Healthy | 96.88 | 96.88 | 96.88 | 96.88 | 93.30 | 96.88 |
Average | 96.65 | 96.65 | 96.65 | 96.65 | 93.30 | 96.65 |
Based on 70% of the TRPH, the HROADL-BCD technique gets average , , , , , and values of 94.32%, 94.29%, 94.32%, 94.28%, 88.61%, and 94.29%, respectively. Based on 30% of TSPH, the HROADL-BCD system obtains average , , , , , and values of 96.65%, 96.65%, 96.65%, 96.65%, 93.30%, and 96.65% respectively.
To calculate the performance of the HROADL-BCD methodology on 80:20 of TRPH/TSPH, TR, and TS curves are shown in Figure 6. The TR and TS curves demonstrate the outcome of the HROADL-BCD method over several epochs. The figure offers related details regarding the learning task and generalizability of the HROADL-BCD system. The TR and TS curves are enhanced with increasing epoch count. The HROADL-BCD approach gets enriched TS accuracy that can identify the patterns in the TR and TS datasets.
The TR and TS loss values of the HROADL-BCD system on 80:20 of TRPH/TSPH over epochs are illustrated in Figure 7. The TR loss depicts that the model loss attained decreased over epochs. The loss value attained was minimized as the model adapted the weight for diminishing the prediction errors for the TR and TS datasets. The loss analysis denotes how well the model fits the TR dataset. TR and TS loss is gradually minimized and defined so that the HROADL-BCD system learns the pattern exposed in the TR and TS data. The HROADL-BCD method adapts the parameter to reduce the variation between the training labels and predictions.
The PR performance of the HROADL-BCD system on 80:20 of TRPH/TSPH is demonstrated by plotting precision against recall as described in Figure 8. The outcome inferred that the HROADL-BCD method obtains high PR values under 2 classes. The result demonstrates that the model identifies different classes. The HROADL-BCD obtains high efficiency in detecting positive instances with reduced false positives.
The ROC examination offered by the HROADL-BCD method on 80:20 of TRPH/TSPH is depicted in Figure 9. The outcome shows valuable insights into the tradeoffs between TPR and FPR rates with divergent classifier thresholds and dissimilar epoch count. It presents the correct predicted solution of the HROADL-BCD method for the classifier of 2 classes.
The cancer detection performance of the HROADL-BCD technique is compared with recent techniques in Table 4 and Figure 10. The simulated values exhibit that the RF, ResNet50, and Inceptionv3 algorithms obtained poorer performance while the SVM, BCDFE-ML, and Efficient-Net systems obtained moderately enhanced results.
Methods | ||||
HROADL-BCD | 97.62 | 97.50 | 97.62 | 97.50 |
OSADL-BCDC | 95.00 | 95.02 | 95.00 | 95.00 |
RF | 69.05 | 75.69 | 79.07 | 77.71 |
SVM | 92.59 | 90.63 | 93.58 | 93.13 |
BCDFE-ML | 92.48 | 92.70 | 89.17 | 93.83 |
ResNet50 | 82.57 | 81.02 | 78.92 | 81.75 |
InceptionV3 | 83.33 | 81.48 | 89.74 | 78.10 |
Efficient-Net | 85.79 | 82.28 | 91.53 | 83.61 |
The OSADL-BCDC model has shown considerable outcomes. However, the HROADL-BCD technique achieves better results with raised , , , and of 97.62%, 97.50%, 97.62%, and 97.50%, respectively. Therefore, the HROADL-BCD technique exhibits optimal performance in the bone cancer detection and classification process.
In this manuscript, an automated bone cancer detection method called the HROADL-BCD technique on X-ray images is presented. The major aim of the HROADL-BCD technique is to inspect the X-ray images for bone cancer detection. In the presented HROADL-BCD method, dissimilar phases of operations are BF-based noise removal, EfficientNet feature extraction, HROA-based tuning, and ABiLSTM-based classification. For hyperparameter tuning of the EfficientNet model, the HROADL-BCD technique uses the HROA. The bone cancer detection and classification process are performed using the ABiLSTM model. For experimental result analysis of the HROADL-BCD system, a wide range of simulations is executed. The extensive outcome inferred the improved outcome of the HROADL-BCD approach concerning various aspects.
The authors declare that they have not used Artificial Intelligence (AI) tools in the creation of this article.
The authors extend their appreciation to the Deputyship for Research and Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project number (IF2/PSAU/2022/01/23005).
The authors declare that they have no conflicts of interest.
T.V.: Conceptualization; P.B.: Data curation; P.B.: Formal analysis; S.S.: Investigation; T.V. and S.S.: Methodology; N.A. and S.M.: Validation; A.M.: Visualization; T.V.: Writing—original draft; P.B.; Writing—review & editing. All authors have read and agreed to the published version of the manuscript.
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Class Name | No. of Instances |
Cancerous | 100 |
Healthy | 100 |
Total No. of Instances | 200 |
Class | MCC | G-Measure | ||||
TRPH (80%) | ||||||
Cancerous | 93.67 | 93.67 | 93.67 | 93.67 | 87.50 | 93.67 |
Healthy | 93.83 | 93.83 | 93.83 | 93.83 | 87.50 | 93.83 |
Average | 93.75 | 93.75 | 93.75 | 93.75 | 87.50 | 93.75 |
TSPH (20%) | ||||||
Cancerous | 95.24 | 100.00 | 95.24 | 97.56 | 95.12 | 97.59 |
Healthy | 100.00 | 95.00 | 100.00 | 97.44 | 95.12 | 97.47 |
Average | 97.62 | 97.50 | 97.62 | 97.50 | 95.12 | 97.53 |
Class | MCC | G-Measure | ||||
TRPH (70%) | ||||||
Cancerous | 93.06 | 95.71 | 93.06 | 94.37 | 88.61 | 94.38 |
Healthy | 95.59 | 92.86 | 95.59 | 94.20 | 88.61 | 94.21 |
Average | 94.32 | 94.29 | 94.32 | 94.28 | 88.61 | 94.29 |
TSPH (30%) | ||||||
Cancerous | 96.43 | 96.43 | 96.43 | 96.43 | 93.30 | 96.43 |
Healthy | 96.88 | 96.88 | 96.88 | 96.88 | 93.30 | 96.88 |
Average | 96.65 | 96.65 | 96.65 | 96.65 | 93.30 | 96.65 |
Methods | ||||
HROADL-BCD | 97.62 | 97.50 | 97.62 | 97.50 |
OSADL-BCDC | 95.00 | 95.02 | 95.00 | 95.00 |
RF | 69.05 | 75.69 | 79.07 | 77.71 |
SVM | 92.59 | 90.63 | 93.58 | 93.13 |
BCDFE-ML | 92.48 | 92.70 | 89.17 | 93.83 |
ResNet50 | 82.57 | 81.02 | 78.92 | 81.75 |
InceptionV3 | 83.33 | 81.48 | 89.74 | 78.10 |
Efficient-Net | 85.79 | 82.28 | 91.53 | 83.61 |
Class Name | No. of Instances |
Cancerous | 100 |
Healthy | 100 |
Total No. of Instances | 200 |
Class | MCC | G-Measure | ||||
TRPH (80%) | ||||||
Cancerous | 93.67 | 93.67 | 93.67 | 93.67 | 87.50 | 93.67 |
Healthy | 93.83 | 93.83 | 93.83 | 93.83 | 87.50 | 93.83 |
Average | 93.75 | 93.75 | 93.75 | 93.75 | 87.50 | 93.75 |
TSPH (20%) | ||||||
Cancerous | 95.24 | 100.00 | 95.24 | 97.56 | 95.12 | 97.59 |
Healthy | 100.00 | 95.00 | 100.00 | 97.44 | 95.12 | 97.47 |
Average | 97.62 | 97.50 | 97.62 | 97.50 | 95.12 | 97.53 |
Class | MCC | G-Measure | ||||
TRPH (70%) | ||||||
Cancerous | 93.06 | 95.71 | 93.06 | 94.37 | 88.61 | 94.38 |
Healthy | 95.59 | 92.86 | 95.59 | 94.20 | 88.61 | 94.21 |
Average | 94.32 | 94.29 | 94.32 | 94.28 | 88.61 | 94.29 |
TSPH (30%) | ||||||
Cancerous | 96.43 | 96.43 | 96.43 | 96.43 | 93.30 | 96.43 |
Healthy | 96.88 | 96.88 | 96.88 | 96.88 | 93.30 | 96.88 |
Average | 96.65 | 96.65 | 96.65 | 96.65 | 93.30 | 96.65 |
Methods | ||||
HROADL-BCD | 97.62 | 97.50 | 97.62 | 97.50 |
OSADL-BCDC | 95.00 | 95.02 | 95.00 | 95.00 |
RF | 69.05 | 75.69 | 79.07 | 77.71 |
SVM | 92.59 | 90.63 | 93.58 | 93.13 |
BCDFE-ML | 92.48 | 92.70 | 89.17 | 93.83 |
ResNet50 | 82.57 | 81.02 | 78.92 | 81.75 |
InceptionV3 | 83.33 | 81.48 | 89.74 | 78.10 |
Efficient-Net | 85.79 | 82.28 | 91.53 | 83.61 |