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A Deep Learning-Based Mobile Application for
Monkeypox Detection
Haifa F. Alhasson * , Elaf Almozainy, Manar Alharbi, Naseem Almansour, Shuaa S. Alharbi
and Rehan Ullah Khan
Department of Information Technology, College of Computer, Qassim University, Buraydah 52571, Saudi Arabia;
392206338@qu.edu.sa (E.A.); 392206339@qu.edu.sa (M.A.); 392206376@qu.edu.sa (N.A.);
shuaa.s.alharbi@qu.edu.sa (S.S.A.); re.khan@qu.edu.sa (R.U.K.)
* Correspondence: hhson@qu.edu.sa
Abstract: The recent outbreak of monkeypox has raised significant concerns in the field of public
health, primarily because it has quickly spread to over 40 countries outside of Africa. Detecting
monkeypox in its early stages can be quite challenging because its symptoms can resemble those of
chickenpox and measles. However, there is hope that potential use of computer-assisted tools may be
used to identify monkeypox cases rapidly and efficiently. A promising approach involves the use of
technology, specifically deep learning methods, which have proven effective in automatically detect-
ing skin lesions when sufficient training examples are available. To improve monkeypox diagnosis
through mobile applications, we have employed a particular neural network called MobileNetV2,
which falls under the category of Fully Connected Convolutional Neural Networks (FCCNN). It
enables us to identify suspected monkeypox cases accurately compared to classical machine learning
approaches. The proposed approach was evaluated using the recall, precision, F score, and accuracy.
The experimental results show that our architecture achieves an accuracy of 0.99%, a Recall of 1.0%,
an F-score of 0.98%, and a Precision of 0.95%. We believe that such experimental evaluation will
contribute to the medical domain and many use cases.
Keywords: artificial neural network; deep learning; detection performance; image analysis; image
classification; machine learning models; neural network; object detectors
Citation: Alhasson, H.F.; Almozainy,
E.; Alharbi, M.; Almansour, N.;
Alharbi, S.S.; Khan, R.U. A Deep
Learning-Based Mobile Application 1. Introduction
for Monkeypox Detection. Appl. Sci.
The Mpox virus, also known as monkeypox, is a type of virus that belongs to the family
2023, 13, 12589. https://doi.org/
Poxviridae and the genus Orthopoxvirus. It is believed that monkeypox is transmitted to
10.3390/app132312589
humans through rodents. The symptoms of monkeypox, such as lesions and rashes, are
Academic Editor: Xianpeng Wang similar to those caused by measles, chickenpox, and smallpox. Due to this similarity, early
Received: 15 October 2023
diagnosis of the disease can be very challenging [1]. However, electron microscopy can
Revised: 15 November 2023
be used to definitively diagnose the virus. It is crucial to isolate individuals who have the
Accepted: 19 November 2023
disease to prevent the spread of the virus [2].
Published: 22 November 2023 Recent outbreaks of the monkeypox virus have caused concern in many parts of the
world. Considering its clinical characteristics, monkeypox closely resembles chickenpox,
measles, and smallpox. The monkeypox virus has gained attention due to its severity and
widespread occurrence. In 1970, a nine-month-old child from the Democratic Republic
Copyright: © 2023 by the authors. of Congo became the first documented case of the disease. Since then, monkeypox has
Licensee MDPI, Basel, Switzerland. become an emerging zoonotic disease that poses a significant public health threat [3]. As
This article is an open access article
a result, outbreaks have increased but are primarily restricted to the continent of Africa.
distributed under the terms and
Due to its rapid spread in more than 40 countries outside of Africa, the recent monkeypox
conditions of the Creative Commons
outbreak has become a public health concern [4]. The transmission of the monkeypox
Attribution (CC BY) license (https://
virus from infected animals to humans has historically been limited due to the need for
creativecommons.org/licenses/by/
close and prolonged contact with wild animals. Human-to-human transmission is rare,
4.0/).
as it typically requires direct interaction with an infected individual. This limited spread
resulted in the disease being confined to specific regions where such interactions occur
regularly. However, recent outbreaks have shown an alarming increase in the number of
monkeypox cases in countries where it was not previously considered endemic [5]. These
outbreaks have highlighted the urgent need for early detection and accurate diagnosis of
monkeypox infections [6]. Monkeypox is a typically self-limiting disease. A monkeypox
rash appears between 1 and 5 days after the onset of the initial signs of monkeypox. The
severity of the disease depends on the amount of virus exposure the patient has received,
their health status, and any complications that occur. As a result, the disease spreads to
other parts of the body. It may be mistaken for chickenpox due to the similarity of the
rashes. Eventually, the rash becomes crusty and begins to spread, making it important to
accurately detect and diagnose monkeypox early on [7,8].
The symptoms of monkeypox, smallpox, and measles are almost identical, as shown in
Figure 1, making it difficult to distinguish them without a laboratory test [9]. Vaccination is
the only way to completely eradicate the disease [10]. While the virus is not life-threatening,
it can cause complications in severe cases, such as sepsis, pneumonia, and blindness [9].
Based on research on virus-related disease detection using Deep Learning (DL) meth-
ods, the majority of studies use the transfer learning approach, which uses well-established
pre-trained DL methods. To the best of our knowledge, there is no extensive research
available on the detection of the monkeypox virus except for the work in ref. [9]. In ref. [9],
interesting results have been achieved. It was determined that the state of the art has three
major limitations.
• Most of the models are limited to binary classification with limited performance.
• There is a limited number of models that offer high accuracy in classifying monkeypox
for quick, real-time diagnosis using smartphones.
• Most of the models have been evaluated using some evaluation metrics in the literature.
The best-performing models in the literature cannot be compared with others and are
not sufficiently generalized, as in ref. [11].
A limited number of research studies have been found to demonstrate the potential of
Machine Learning (ML) methods in diagnosing monkeypox disease using image processing
techniques. In a previous study [12], two main factors were identified as the cause for the
lack of a basis for the advancement of an image-based diagnosis of monkeypox disease:
1. There is a small number of publicly accessible datasets that can be utilized to train and
test to construct an ML model to diagnose monkeypox.
2. Given that the virus has recently gained significant exposure in numerous nations, it is
customary to incorporate a suitable ML algorithm alongside the dataset. Furthermore,
the presentation of a model requires additional time when dealing with image data.
In this article, we evaluate, develop and deploy a mobile application based on DL to
identify and classify monkeypox disease among other skin lesions. From an application
Appl. Sci. 2023, 13, 12589 3 of 16
perspective, monkeypox images can be distinguished from chickenpox and measles images
using pre-trained deep learning networks in the Android mobile application.
The main contribution of this article is a proposed mobile-based deep-learning model
for detecting and classifying monkeypox skin lesions. The model achieves an accurate and
affordable diagnosis, leading to improved treatment outcomes and a reduction in healthcare
costs. It also suggests that deep learning can have broader applications in medical imaging
tasks beyond monkeypox diagnosis.
The rest of the paper is organized as follows: Section 2 provides an explanation of
the deep learning-based approaches utilized in this paper with details of dataset used
to evaluate the method. Details of the results related to the discussion are provided in
Section 3. Section 4 concludes the article.
Akin et al. [23] analyzed monkeypox skin lesions using an AI-assisted CNN. ResNet-18,
ResNet-50, VGG- 16, Densenet-161, EfficientNet B7, EfficientNet V2, GoogLeNet, MobileNet
V2, MobileNet V3, ResNeXt-50, ShuffleNetV2, and ConvNeXt were used in the experiments.
This resulted in the MobileNetV2 model having the best accuracy compared with the other
modules. Islam et al. [13] proposed a web-scraping-based data collection system for a
monkeypox skin lesion. In the classification task, ResNet50, Inception-V3, DenseNet121,
MnasNet-A1, MobileNet-V2, ShuffleNet-V2, and SqueezeNet models were used. The
ShuffleNet-V2 outperformed the other modules.
Ahsan et al. [24] generated a new monkeypox classification dataset. Based on the
1915 augmented images, the VGG16 model was implemented. Ali et al. [10] applied
different deep learning modules to the MSID dataset in order to classify monkeypox. These
modules included VGG16, ResNet50, Inception-V3, and ResNet50. The ResNet50 achieved
the best accuracy compared to other modules.
Sahin et al. [21] presented an android mobile application, using a smartphone camera
to detect and classify the monkey-pox. They used four different DL networks VGG16,
ResNet50, InceptionV3, and Ensemble. In their experiment, EfficientNetb0 and Mo-
bileNetv2 showed better performance in terms of accuracy compared to other modules.
Haque et al. [25] applied the MSLD dataset to different transfer-learning-based models
using VGG19, DenseNet121, Xception, EfficientNetB3, and MobileNetV2. Ali et al. [10]
analyzed monkeypox skin lesions and other diseases (chickenpox, measles) using pre-
trained models such as VGG-16, ResNet50, and InceptionV3. On another hand, Hus-
sain et al. [22] compared the performance of monkeypox classification using wide range of
modules: ResNet50, DenseNet121, Inception-V3, SqueezeNet, MnasNet-A1, MobileNet-V2
and ShuffleNet-V2. Ahsan et al. [9] applied a modified VGG16 to identify monkeypox.
They applied feature extraction and prediction using Local Interpretable Model-Agnostic
Explanations (LIME). Sitaula et al. [11] introduced a new method based on DenseNet-169
and Xception on the monkeypox-2022 image dataset, whereas Bajwa et al. [26] utilized
DenseNet-161, ResNet-152, NASNet, and SE ResNeXt-101 in the DermNet dataset.
Manne et al. [27], reviews several articles using CNNs to classify skin lesions. Recently,
machine learning algorithms have reduced the rate of misclassification of skin lesions
compared to dermatologists. In our paper, we also present the use of CNNs in successfully
classifying skin cancer types, as well as the methods that have been implemented and the
success rate. Rajput et al. [28] proposed an efficient convolutional neural network (CNN)
model for identifying skin cancer problems with high accuracy. In order to classify the
HAM10K data, the AlexNet model has been customized.
Other methods that are designed to utilize a collection of transfer learning modules
to improve the classification task are discussed in [29,30]. Raza et al. [29] introduced an
ensemble model for the classification of skin lesions. Their module includes the use of hyper-
transfer learning methods such as Xception, Inceptionv3, DenseNet121, and DenseNet201.
On the other hand, Gouda et al. [30] presents a new method called ESRGAN that classifies
images using Resnet50, InceptionV3, and Inception Resnet. Table 1 summarizes the various
approaches used in previous studies, along with the techniques applied and the datasets
used to evaluate the models.
Appl. Sci. 2023, 13, 12589 5 of 16
Additional
Research Paper Network Used and Accuracy Value (%) Dataset Used Evaluation
Measurement
ResNet18 (86.8%), GoogleNet (82.22%),
1-fold
Sahin et al. [21] EfficientNetb0 (91.11%), NasnetMobile (86.67%), Prepared
cross-validation
ShuffleNet (80.00%), MobileNetv2 (91.11%)
Precision, Recall,
Manjurul et al. [12] VGGNet (71%), MobileNet (94.4%) MSLD F1-score and
Specificity
VGG19-CBAM-Dense (71.86%), Xception
CBAM-Dense (83.89%),
Monkey-pox Skin,
DenseNet121-CBAM-Dense (78.27%), 4-fold
Haque et al. [25] Lesion
MobileNetV2-CBAM-Dense (74.07%), cross-validation
Dataset (MSLD)
EfficientNetB3CBAMDense (81.43%), Ensemble (79.26%),
ShuffleNet (80.00%)
Xception (96.83%), Resnet50 (96.93%),
Almuayqil et al. [31] DenseNet201 (97.16%), InceptionV3 (96.62%), Prepared –
VGG19 (96.97%), InceptionResnet (96.65%)
ResNet-18 (98.25%), ResNet50 (96.49%), VGG-16 (92.98%),
Densenet-161 (96.49%), EfficientNetB7 (94.74%),
Monkey-pox Skin,
GogLeNet (96.49%), EfficientNetV2 (96.49%),
Akin et al. [23] Images Sensitivity
MobileNetV2 (98.25%), MobileNetV3 (75.44%),
Dataset (MSID)
ResNeXt-50 (92.98%), ShuffleNetV2 (78.95%),
ConvNeXt (96.49%)
VGG16 (0.93%), InceptionResNetV2 (0.98%),
Ahsan et al. [9] ResNet50 (0.72%), ResNet101 (0.72%), Prepared Precision
MobileNetV2 (0.99%), VGG19 (0.90%)
ResNet50 (0.72%), Inception-V3 (0.71%),
DenseNet121 (0.78%), MnasNet-AI (0.72%), 5-fold
Hussain et al. [22] Prepared
MobileNet-V2 (0.77%), ShuffleNet-V2 (0.79%), cross-validation
SqueezeNet (0.65%)
1.3. DL Approaches
1.3.1. CNN
Utilizing deep learning (DL) techniques enables the automated acquisition of complex
features necessary for visual pattern recognition. Convolutional neural networks (CNNs),
a specific type of DL approach, have been extensively employed in various computer
vision tasks, encompassing facial expression recognition, text recognition, face recognition,
gender classification, age classification, and action recognition. Moreover, CNNs have
exhibited remarkable performance in biomedical applications, specifically in the domains
of pattern recognition and computer vision. Different CNN architectures employ different
combinations of convolutional, pooling, and fully connected layers. The convolutional
process involves the conversion of input data into filters [21,32]. The convolution process is
visually depicted in Figure 2.
Suppose a square neuron layer is followed by a convolutional layer. If we use a m × m
filter w, our convolutional layer output will be of the size ( N − m + 1) × ( N − m + 1).
To calculate the pre-nonlinearity input to a unit x l ij in our layer, we must sum up the
contributions (weighted by the filter components) from the previous layer cells.
m −1 m −1
xijl = ∑ ∑ wab yl(− 1
i + a)( j+b)
(1)
a =0 b =0
Appl. Sci. 2023, 13, 12589 6 of 16
1.3.2. MobileNetV2
Howard et al. [33,34] introduced a class of efficient models designed for applications
involving mobile and embedded vision, which they call MobileNets. These MobileNets
are built upon a simplified architecture that utilizes depth-wise separable convolutions
to construct deep and lightweight neural networks. The key idea behind depth-wise
separable convolution is that it achieves the same output as the conventional convolution
method but with increased efficiency. This efficiency arises from a reduction in the number
of parameters involved in the computation, as in ref. [33]. Furthermore, the authors
incorporate inverted residual layers into their network architecture. These layers are added
right after the initial convolution layer and feature 32 filters. This is then followed by
a pointwise convolution which produces output with a size of 7 × 7 × 1280 pixels. In
convolutional networks, residual blocks serve to convey information from the beginning
to the end of the convolutional block using a skip-connection. It is commonly observed
that the layers between the beginning and end of a residual block have more channels
than those between the beginning and end of the residual block. MobileNetV2 uses an
inverted residual block in which the connected layers have fewer channels than the layers
between, resulting in a much lower number of parameters than the standard residual block.
Therefore, the authors present two simple global hyperparameters that are designed to
efficiently trade off latency and accuracy. By selecting these hyperparameters, the model
creator is able to select the appropriate model size for their application based on the
constraints of the problem.
Under the same level of complexity, MobileNet performs inference significantly faster.
When the computational resources are relatively low, MobileNet uses a slow down sampling
strategy, which causes severe performance degradation. MobileNetV2 takes input images
with the size of 224 × 224 × 3 pixels. Therefore, the input images on the dataset have to be
resized and cropped. Figure 3 shows the architecture of MobileNet that contains several
convolutional blocks.
the base network or model are generally frozen. In the last layer of the network, which
is usually a fully connected layer, the network is trained to learn the specific features of
the new dataset. A number of layers are added to the base model, called the head model,
which improves the performance of the network.
2. Methods
2.1. Datasets
In order to train and test the proposed model, the focus is on two datasets from the
literature as shown in Table 2. Furthermore, our aim is to make the chosen dataset different
in terms of clarity, illumination, shadow, and noise. Therefore, we use two datasets.
we acquired a diverse and large dataset. For experimental evaluation, we used Kaggle’s
MSID Monkeypox Skin Image Dataset, which consists of 770 images and is comparatively
state of the art for the detection of monkeypox. We split the dataset into three parts: training
(40%), validation (20%), and testing (20%), before conducting augmentation to avoid any
inducing bias to the model performance results. Then, we applied Data Augmentation to
the dataset and increased the number of images to 4074 before dividing the images into
four categories. Figure 4a,b display some sample images from MSID and MSLD datasets.
Figure 5. Augmentation approaches used on MSID dataset. (a) Resizing and grayscale effect,
(b) resizing and rotation effect, and (c) resizing and saturation effect.
Appl. Sci. 2023, 13, 12589 9 of 16
Previous studies have highlighted the problem of class imbalances [37], where some
classes had significantly higher volumes than others. The dataset was balanced using
SMOTETomek [38], which combines oversampling and under-sampling techniques. Prior
to implementing the SMOTETomek technique, the target variable count was found to be
imbalanced, as indicated in (Supplementary Materials, Figure S1a). The method involves
combining oversampling and undersampling techniques to generate synthetic samples
for minority classes, as well as removing noisy samples from majority classes. As shown
in (Supplementary Materials, Figure S1b), the SMOTETomek technique has resulted in a
target variable count of 1220–1356 for all classes.
Figure 6. The structure of our model using samples of MSID dataset [24].
Appl. Sci. 2023, 13, 12589 10 of 16
Hyperparameters Value
Learning rate 0.001
Optimizer Adamax
Activation function Softmax
Regularizers L2 (0.01)
Early stopping Yes
Batch size 128
Dropout 0.2
Dense activation function ReLU
Appl. Sci. 2023, 13, 12589 11 of 16
Table 5. F1-score, Recall, and Precision testing results for all classes.
epoch epoch
(a) Training vs. validation loss (b) Training vs. validation accuracy
Figure 8. Performance of the training process and validation of the proposed method on MSID dataset.
accuracy, recall, precision, auc
epoch
Figure 9. A graph showing the highest score among the evaluation metrics used in the study.
Appl. Sci. 2023, 13, 12589 13 of 16
costs, and facilitating prompt diagnoses across various ailments. This study also highlights
the potential significance of deep learning in other medical imaging tasks.
Nevertheless, it is important to acknowledge the limitations of this study. One limi-
tation is the relatively small sample size in the dataset used and its applicability to other
datasets. Another limitation is that the dataset utilized solely consists of pox-related images
without any samples of “no skin lesions”. Future research should consider incorporating
larger and more diverse datasets that include various types of skin lesions as well as cases
without any skin lesions for a comprehensive analysis. Furthermore, it would be valuable
to evaluate the performance of the proposed model on different platforms and devices to
ensure its practicality and scalability.
4. Conclusions
The recent monkeypox outbreak has become a major cause for concern within the field
of public health, particularly due to its rapid spread to more than 40 countries outside of
Africa. Detecting monkeypox in its early stages presents a significant challenge because
its symptoms can easily be mistaken for those of chickenpox and measles. One promising
avenue is the use of computer-assisted tools, specifically harnessing the power of deep
learning methods. These methods have already demonstrated their effectiveness in auto-
matically identifying skin lesions, provided they are trained with sufficient examples. To
contribute to the diagnosis of monkeypox through easily accessible mobile applications, in
this article, we used a specific type of neural network known as MobileNetV2.
Our proposed approach was rigorously evaluated using various metrics, including
Recall, Precision, F-score, and accuracy. The experimental results showed the effectiveness
of our proposed approach: our architecture achieved an astonishing precision rate of 99%, a
perfect recall rate of 100%, an F-score of 98%, and a high precision rate of 95%. These results
underscore the potential of deep learning and MobileNetV2 as valuable tools in the battle
against monkeypox, offering both precision and efficiency in diagnosis. We believe that
such experimental evaluation will contribute to the medical domain and many use cases.
Supplementary Materials: The following supporting information can be downloaded at: https://www.
mdpi.com/article/10.3390/app132312589/s1, Figure S1: The distribution of skin disease classes in
the MSID dataset before and after augmentation (a) before augmentation and (b) after augmentation.;
Figure S2:An illustration of different use cases in the application.; Table S1: The description of used
evaluation metrics in the study.
Author Contributions: Methodology, H.F.A., E.A., M.A. and N.A.; Software, E.A., M.A., N.A. and
H.F.A.; Validation, E.A., M.A. and N.A.; Writing—original draft, H.F.A.; Writing—review & editing,
H.F.A., S.S.A. and R.U.K.; Supervision, H.F.A.; Project administration, H.F.A. All authors have read
and agreed to the published version of the manuscript.
Funding: The researchers would like to thank the Deanship of Scientific Research, Qassim University
for funding the publication of this project.
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.
Data Availability Statement: The data presented in this study are available in the article.
Conflicts of Interest: The authors declare no conflict of interest.
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