A Support Vector Machine (SVM) based approach for microgrid islanding decision and control is investigated. The IEEE 13-feeder system is modified and serves as the microgrid model connected to Kundur four-machine two-area system that models the main transmission grid. A representative data set is obtained through simulations in MATLAB/Simulink considering multiple typical scenarios with or without a fault. A SVM classifier is designed to identify insecure scenarios with satisfying accuracy. Comparisons between different kernel functions are then carried out, which indicate that linear SVM can be effective for the islanding control. The SVM approach is further compared with a decision tree based approach in terms of training and testing accuracies for the microgrid islanding control problem.
This paper proposes a passive islanding detection technique for microgrid. The proposed technique relies on capturing the underlying signatures of a wide variety of system events on critical system parameters through the utilization of pattern recognition tools for islanding detection in a microgrid. The proposed technique is tested on a microgrid model implemented on IEEE 13-node distribution feeder system under a wide variety of system operating states. Results from test case study have been analyzed to evaluate the effectiveness of the proposed method. Case study results indicate that the proposed method can detect islanding events with high accuracy and reliability.
The present study emphasizes the efficacy of a biosurfactant-producing bacterial strain Klebsiella sp. KOD36 in biodegradation of azo dyes and hexavalent chromium individually and in a simultaneous system. The bacterial strain has exhibited a considerable potential for biodegradation of chromium and azo dyes in single and combination systems (maximum 97%, 94% in an individual and combined system, respectively). Simultaneous aerobic biodegradation of azo dyes and hexavalent chromium (SBAHC) was modeled using machine learning programming, which includes gene expression programming, random forest, support vector regression, and support vector regression-fruit fly optimization algorithm. The correlation coefficient includes the dispersion index, and the Willmott agreement index was employed as statistical metrics to assess the performance of each model separately. In addition, the Taylor diagram was used to further investigate the methods used. The findings of the present study were that the support vector regression-fruitfly optimization algorithm (SVR-FOA) with correlation coefficient (CC) of 0.644, (scattered index) SI of 0.374, and (Willmott’s index of agreement) WI of 0.607 performed better than the autonomous support vector regression (SVR), gene expression programming (GEP), and random forest (RF) methods. In addition, the standalone SVR model with CC of 0.146, SI of 0.473, and WI of 0.408 ranked the second best. In summary, the SBAHC can be accurately estimated using the hybrid SVR-FOA method. In other words, FOA has proven to be a powerful optimization algorithm for increasing the accuracy of the SVR method.
Stenotrophomonas maltophilia is a multidrug resistant pathogen associated with high mortality and morbidity in patients having compromised immunity. The efflux systems of S. maltophilia include SmeABC and SmeDEF proteins, which assist in acquisition of multiple-drug-resistance. In this study, proteome based mapping was utilized to find out the potential drug targets for S. maltophilia strain k279a. Various tools of computational biology were applied to remove the human-specific homologous and pathogen-specific paralogous sequences from the bacterial proteome. The CD-HIT analysis selected 4315 proteins from total proteome count of 4365 proteins. Geptop identified 407 essential proteins, while the BlastP revealed approximately 85 non-homologous proteins in the human genome. Moreover, metabolic pathway and subcellular location analysis were performed for essential bacterial genes, to describe their role in various cellular processes. Only two essential proteins (Acyl-[acyl-carrier-protein]—UDP-N acetyl glucosamine O-acyltransferase and D-alanine-D-alanine ligase) as candidate for potent targets were found in proteome of the pathogen, in order to design new drugs. An online tool, Swiss model was employed to model the 3D structures of both target proteins. A library of 5000 phytochemicals was docked against those proteins through the molecular operating environment (MOE). That resulted in to eight inhibitors for both proteins i.e. enterodiol, aloin, ononin and rhinacanthinF for the Acyl-[acyl-carrier-protein]—UDP-N acetyl glucosamine O-acyltransferase, and rhazin, alkannin beta, aloesin and ancistrocladine for the D-alanine-D-alanine ligase. Finally the ADMET was done through ADMETsar. This study supported the development of natural as well as cost-effective drugs against S. maltophilia. These inhibitors displayed the effective binding interactions and safe drug profiles. However, further in vivo and in vitro validation experiment might be performed to check their drug effectiveness, biocompatibility and their role as effective inhibitors.
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