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The Gene Ontology (GO) analysis of the miRNA with affiliation to NSP3 suggests that these miRNAs show strongly significantly enriched GO terms related to the known symptoms of COVID-19. Docking and MD simulation study of the obtained miRNA through high-throughput analysis suggest a non-coding RNA (an RNA antitoxin, ToxI) as a natural aptamer drug candidate for NSP5 inhibition. Finally, a significant interplay of the host RNA-viral protein in the host cell can disrupt the host cell's system by influencing the RNA-dependent processes of the host cells, such as a differential expression in RNA. Furthermore, our results are useful to identify the side effects of mRNA-based vaccines, many of which are caused by the off-label interactions with the human lncRNAs.Bacterial diseases are considered by the World Health Organization to be one of the greatest threats to public health worldwide, mainly due to the increasingly frequent resistance to traditional antibiotics. Estimates from the World Bank indicate that the annual global economic impacts of antibiotic resistance will reach US$1.0-3.4 trillion by 2030. With this, the demand for studies aiming at the discovery of new antibiotics or molecules that may play a synergistic role within the spectrum of drug-resistant bacteria is of fundamental importance. In this in silico study, ligands generated from anthraquinones with established antibacterial activity were evaluated as potential inhibitors of the DNA gyrase subunit B of two species of Gram-positive and two Gram-negative bacteria. The main result of molecular docking-based virtual screening reveals several anthraquinones with remarkable binding energies, of which 7,7'-bializarin (ZINC000004783172) exhibited the highest value for all DNA gyrases subunit B studied and formed stable complexes, as evidenced by molecular dynamics simulations. Collectively, the results presented here reveal the potential of this molecule to bind tightly to the active site of DNA gyrases subunit B of Escherichia coli, Salmonella enterica (subtype typhi), Enterococcus faecalis, and Staphylococcus aureus, and therefore represents a promising candidate for further in vitro testing aimed at evaluating its antibacterial effect.Breast cancer is the second most common cancer in the world. Early diagnosis and treatment increase the patient's chances of healing. The temperature of cancerous tissues is generally different from that of healthy neighboring tissues, making thermography an option to be considered in the fight against cancer because it does not use ionizing radiation, venous access, or any other invasive process, presenting no damage or risk to the patient. In this paper, we propose a hybrid computational method using the Dynamic Infrared Thermography (DIT) and Static Infrared Thermography (SIT) for abnormality screening and diagnosis of malignant tumor (cancer), applying supervised and unsupervised machine learning techniques. We use the area under receiver operating characteristic curve, sensitivity, specificity, and accuracy as performance measures to compare the hybrid methodology with previous work in the literature. Wnt agonist 1 molecular weight The K-Star classifier achieved accuracy of 99% in the screening phase using DIT images. The Support Vector Machines (SVM) classifier applied on SIT images yielded accuracy of 95% in the diagnosis of cancer. The results confirm the potential of the proposed approaches for screening and diagnosis of breast cancer.The application of machine learning (ML) techniques to digitized images of biopsied cells for breast cancer diagnosis is an active area of research. We hypothesized that reducing noise in the data would lead to an increase in classification accuracies. To test this hypothesis, we first compared several classification techniques in their ability to discriminate between malignant and benign breast cancer tumors using the Wisconsin Breast Cancer Data Set and subsequently evaluated the effect of noise reduction techniques on model accuracies. We applied two noise-reduction techniques based on Principal Component Analysis - dimensionality reduction and outlier removal - to a comprehensive list of ML algorithms with different learning paradigms including Decision Trees (fine, medium, coarse), dimensionality reduction techniques (Linear Discriminant Analysis, Quadratic Discriminant Analysis, Partial Least Squares-Discriminant Analysis), logistic Regression, Bayesian techniques (Gaussian Naive, Kernel Naive), Supportng a ML algorithm.Low-dose computed tomography (LDCT) imaging can greatly reduce the radiation dose imposed on the patient. However, image noise and visual artifacts are inevitable when the radiation dose is low, which has serious impact on the clinical medical diagnosis. Hence, it is important to address the problem of LDCT denoising. Image denoising technology based on Generative Adversarial Network (GAN) has shown promising results in LDCT denoising. Unfortunately, the structures and the corresponding learning algorithms are becoming more and more complex and diverse, making it tricky to analyze the contributions of various network modules when developing new networks. In this paper, we propose a progressive Wasserstein generative adversarial network to remove the noise of LDCT images, providing a more feasible and effective way for CT denoising. Specifically, a recursive computation is designed to reduce the network parameters. Moreover, we introduce a novel hybrid loss function for achieving improved results. The hybrid loss function aims to reduce artifacts while better retaining the details in the denoising results. Therefore, we propose a novel LDCT denoising model called progressive Wasserstein generative adversarial network with the weighted structurally-sensitive hybrid loss function (PWGAN-WSHL), which provides a better and simpler baseline by considering network architecture and loss functions. Extensive experiments on a publicly available database show that our proposal achieves better performance than the state-of-the-art methods.In conventional medical image printing methods, volumetric medical data needs to be conversed into STereo Lithography (STL) format, the most commonly used format for representing geometric models for 3D printing. However, this STL conversion process is not only time consuming, but more importantly, it often leads to the loss of accuracy. It has become a critical factor hindering the printing efficiency and precision of organ models. By examining the key characteristics of discrete medical volume data, this paper proposes a direct slicing technique for printing implicitly represented 3D medical models. The proposed method mainly consists of three algorithms (1) A layer-based contour extraction algorithm for discrete volume data; (2) An inner shell construction algorithm based on discrete point differential indentation; (3) An infill generation algorithm based on the constructed virtual contour and scan lines. The proposed method has been applied to the slicing of several organ models for experiments, and the ratios of time cost and memory cost between the conventional method and the proposed method are about 4-100 and 1.
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