The coronavirus (COVID-19) pandemic is putting healthcare systems across the world under unprecedented and increasing pressure according to the World Health Organization (WHO). With the advances in computer algorithms and especially Artificial Intelligence, the detection of this type of virus in the early stages will help in fast recovery and help in releasing the pressure off healthcare systems. In this paper, a GAN with deep transfer learning for coronavirus detection in chest X-ray images is presented. The lack of datasets for COVID-19 especially in chest X-rays images is the main motivation of this scientific study. The main idea is to collect all the possible images for COVID-19 that exists until the writing of this research and use the GAN network to generate more images to help in the detection of this virus from the available X-rays images with the highest accuracy possible. The dataset used in this research was collected from different sources and it is available for researchers to download and use it. The number of images in the collected dataset is 307 images for four different types of classes. The classes are the COVID-19, normal, pneumonia bacterial, and pneumonia virus. Three deep transfer models are selected in this research for investigation. The models are the Alexnet, Googlenet, and Restnet18. Those models are selected for investigation through this research as it contains a small number of layers on their architectures, this will result in reducing the complexity, the consumed memory and the execution time for the proposed model. Three case scenarios are tested through the paper, the first scenario includes four classes from the dataset, while the second scenario includes 3 classes and the third scenario includes two classes. All the scenarios include the COVID-19 class as it is the main target of this research to be detected. In the first scenario, the Googlenet is selected to be the main deep transfer model as it achieves 80.6% in testing accuracy. In the second scenario, the Alexnet is selected to be the main deep transfer model as it achieves 85.2% in testing accuracy, while in the third scenario which includes two classes (COVID-19, and normal), Googlenet is selected to be the main deep transfer model as it achieves 100% in testing accuracy and 99.9% in the validation accuracy. All the performance measurement strengthens the obtained results through the research.

The Coronavirus disease 2019 (COVID-19) is the fastest transmittable virus caused by severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2). The detection of COVID-19 using artificial intelligence techniques and especially deep learning will help to detect this virus in early stages which will reflect in increasing the opportunities of fast recovery of patients worldwide. This will lead to release the pressure off the healthcare system around the world. In this research, classical data augmentation techniques along with Conditional Generative Adversarial Nets (CGAN) based on a deep transfer learning model for COVID-19 detection in chest CT scan images will be presented. The limited benchmark datasets for COVID-19 especially in chest CT images are the main motivation of this research. The main idea is to collect all the possible images for COVID-19 that exists until the very writing of this research and use the classical data augmentations along with CGAN to generate more images to help in the detection of the COVID-19. In this study, five different deep convolutional neural network-based models (AlexNet, VGGNet16, VGGNet19, GoogleNet, and ResNet50) have been selected for the investigation to detect the Coronavirus-infected patient using chest CT radiographs digital images. The classical data augmentations along with CGAN improve the performance of classification in all selected deep transfer models. The outcomes show that ResNet50 is the most appropriate deep learning model to detect the COVID-19 from limited chest CT dataset using the classical data augmentation with testing accuracy of 82.91%, sensitivity 77.66%, and specificity of 87.62%.

Cancer is one of the most feared and aggressive diseases in the world and is responsible for more than 9 million deaths universally. Staging cancer early increases the chances of recovery. One staging technique is RNA sequence analysis. Recent advances in the efficiency and accuracy of artificial intelligence techniques and optimization algorithms have facilitated the analysis of human genomics. This paper introduces a novel optimized deep learning approach based on binary particle swarm optimization with decision tree (BPSO-DT) and convolutional neural network (CNN) to classify different types of cancer based on tumor RNA sequence (RNA-Seq) gene expression data. The cancer types that will be investigated in this research are kidney renal clear cell carcinoma (KIRC), breast invasive carcinoma (BRCA), lung squamous cell carcinoma (LUSC), lung adenocarcinoma (LUAD) and uterine corpus endometrial carcinoma (UCEC). The proposed approach consists of three phases. The first phase is preprocessing, which at first optimize the high-dimensional RNA-seq to select only optimal features using BPSO-DT and then, converts the optimized RNA-Seq to 2D images. The second phase is augmentation, which increases the original dataset of 2086 samples to be 5 times larger. The selection of the augmentations techniques was based achieving the least impact on manipulating the features of the images. This phase helps to overcome the overfitting problem and trains the model to achieve better accuracy. The third phase is deep CNN architecture. In this phase, an architecture of two main convolutional layers for featured extraction and two fully connected layers is introduced to classify the 5 different types of cancer according to the availability of images on the dataset. The results and the performance metrics such as recall, precision and F1 score show that the proposed approach achieved an overall testing accuracy of 96.90%. The comparative results are introduced, and the proposed method outperforms those in related works in terms of testing accuracy for 5 classes of cancer. Moreover, the proposed approach is less complex and consume less memory.

Multi-access edge computing (MEC) brings many services closer to user devices, alleviating the pressure on resource-constrained devices. It enables devices to offload compute-intensive tasks to nearby MEC servers. Hence, improving users’ quality of experience (QoS) by reducing both application execution time and energy consumption. However, to meet the huge demands, efficient resource scheduling algorithms are an essential and challenging problem. Resource scheduling involves efficiently allocating and managing MEC resources. In this paper, we survey the state-of-the-art research regarding this issue and focus on deep reinforcement learning (DRL) solutions. DRL algorithms reach optimal or near-optimal policies when adapted to a particular scenario. To the best of our knowledge, this is the first survey that specifically focuses on the use of RL and DRL techniques for resource scheduling in multi-access computing. We analyze recent literature in three research aspects, namely, content caching, computation offloading, and resource management. Moreover, we compare and classify the reviewed papers in terms of application use cases, network architectures, objectives, utilized RL algorithms, evaluation metrics, and model approaches: centralized and distributed. Furthermore, we investigate the issue of user mobility and its effect on the model. Finally, we point out a few unresolved research challenges and suggest several open research topics for future studies.

Early detection of cancer increases the probability of recovery. This paper presents an intelligent decision support system (IDSS) for the early diagnosis of cancer based on gene expression profiles collected using DNA microarrays. Such datasets pose a challenge because of the small number of samples (no more than a few hundred) relative to the large number of genes (in the order of thousands). Therefore, a method of reducing the number of features (genes) that are not relevant to the disease of interest is necessary to avoid overfitting. The proposed methodology uses the information gain (IG) to select the most important features from the input patterns. Then, the selected features (genes) are reduced by applying the grey wolf optimization (GWO) algorithm. Finally, the methodology employs a support vector machine (SVM) classifier for cancer type classification. The proposed methodology was applied to two datasets (Breast and Colon) and was evaluated based on its classification accuracy, which is the most important performance measure in disease diagnosis. The experimental results indicate that the proposed methodology is able to enhance the stability of the classification accuracy as well as the feature selection.