The in-medium masses of the kaons and antikaons in strongly magnetized asymmetric nuclear matter are studied using a chiral SU(3) model. The medium modifications of the masses of these open strange pseudoscalar mesons arise due to their interactions with the nucleons and scalar mesons within the model. The effects of anomalous magnetic moments (AMM) of the nucleons are taken into consideration in the present study and these are seen to be large at high magnetic fields and high densities. The isospin effects are appreciable at high densities. The density effects are observed to be the dominant medium effects, as compared to the effects from magnetic field and isospin asymmetry.
Alzheimer's disease is a non-reversible, non-curable, and progressive neurological disorder that induces the shrinkage and death of a specific neuronal population associated with memory formation and retention. It is a frequently occurring mental illness that occurs in about 60%-80% of cases of dementia. It is usually observed between people in the age group of 60 years and above. Depending upon the severity of symptoms the patients can be categorized in Cognitive Normal (CN), Mild Cognitive Impairment (MCI) and Alzheimer's Disease (AD). Alzheimer's disease is the last phase of the disease where the brain is severely damaged, and the patients are not able to live on their own. Radiomics is an approach to extracting a huge number of features from medical images with the help of data characterization algorithms. Here, 105 number of radiomic features are extracted and used to predict the alzhimer's. This paper uses Support Vector Machine, K-Nearest Neighbour, Gaussian Naïve Bayes, eXtreme Gradient Boosting (XGBoost) and Random Forest to predict Alzheimer's disease. The proposed random forest-based approach with the Radiomic features achieved an accuracy of 85%. This proposed approach also achieved 88% accuracy, 88% recall, 88% precision and 87% F1-score for AD vs. CN, it achieved 72% accuracy, 73% recall, 72% precisionand 71% F1-score for AD vs. MCI and it achieved 69% accuracy, 69% recall, 68% precision and 69% F1-score for MCI vs. CN. The comparative analysis shows that the proposed approach performs better than others approaches.
Ion channels are ion-permeable protein pores that are found in all cell lipid membranes. Distinct ion channels play multiple roles in biological processes.Proteomic data is fast accumulating as a result of the fast growth of mass spectrometry and giving us the chance to comprehensively explore ion channel classes along with their subclasses. This paper proposes an eXtreme Gradient Boosting (XGBoost)-based method to estimate the ion channel classes and their subclasses. Here, 12 feature vectors are applied to better characterize protein sequences like amino acid composition, pseudo-amino acid composition, normalized moreau-broto autocorrelation, amphiphilic pseudo-amino acid composition, dipeptide composition, Geary autocorrelation, tripeptide composition, sequence-order-coupling number, composition/transition/distribution, conjoint triad, moran autocorrelation, quasisequence-order descriptors. Here, a total of 9920 features are extracted from the protein sequence. The principal component analysis is applied to determine the optimal number of features to optimize the performance. In 10-fold cross-validation the proposed XGBoost based approach with optimal 50 features achieved accuracy of 100%, 98.70%, 98.77%, 97.26%, 87.40%, 97.39%, 98.03%, 96.42%, and F1-Score of 100%, 99%, 99%, 97%, 87%, 97%, 98%, 97%, for prediction of ion channel and nonion channel, voltage-gated and ligand-gated ion channels, subclasses of voltage-gated ion channels (VGICs), subclasses of ligand-gated ion channels (LGICs), subclasses of voltage-gated calcium channels (VGCCs), subclasses of voltage-gated potassium channels (VGKCs), subclasses of voltage-gated sodium channels (VGSCs), and subclasses of voltage-gated chloride channels, respectively. Here the proposed approach also compares with the other approaches such as support vector machine, k-nearest neighbor, Gaussian Naïve Bayes, and random forest and also compares with existing methods such as support vector machine (SVM) with maximum relevance maximum distance with an accuracy of 86.6%, 83.7%, and 85.1%, for ion channels, non-ion channels and overall respectively and SVM with radial basis function kernel-based method with an accuracy of 100%, 97% and 99.9% for ion channels, nonion channels, and overall accuracy, respectively.
Proteins are fundamental compounds in biological processes during the analysis of drug target indication for drug repurposing. The identification of relevant features is a necessary step in determining protein structure. A classification technique is used to identify the most important features in a dataset, which is why feature selection is so important. For protein structure prediction, recent research has developed a wide range of new methods to improve accuracy. The authors use principal component analysis (PCA) with correlation-matrix-based feature selection to analyse breast cancer data. In this paper, they discussed a therapeutic agent that is used to reduce the dataset by reduction-based algorithm and after that applied reduced dataset labelled as Standard Gold Dataset on machine learning model to analyze drug target indication. They get the higher accuracy of 92.8%, 93.9%, and 95.3%, each of the three datasets with 200, 500, and 1000 features with SVM with RBF kernel function. Also they found the best result, 97.8%, with the same classifier.
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