119 research outputs found

    An Overview of Electricity Demand Forecasting Techniques

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    Load forecasts are extremely important for energy suppliers and other participants in electric energy generation, transmission, distribution and markets. Accurate models for electric power load forecasting are essential to the operation and planning of a utility company. Load forecasts are extremely important for energy suppliers and other participants in electric energy generation, transmission, distribution and markets. This paper presents a review of electricity demand forecasting techniques. The various types of methodologies and models are included in the literature. Load forecasting can be broadly divided into three categories: short-term forecasts which are usually from one hour to one week, medium forecasts which are usually from a week to a year, and long-term forecasts which are longer than a year.  Based on the various types of studies presented in these papers, the load forecasting techniques may be presented in three major groups: Traditional Forecasting technique, Modified Traditional Technique and Soft Computing Technique. Keywords: Electricity Demand, Forecasting Techniques, Soft Computing, Regression method, SVM

    ISOLATION AND CHARACTERIZATION OF ACTINOMYCETES FROM SOIL OF AD-DAWADMI, SAUDI ARABIA AND SCREENING THEIR ANTIBACTERIAL ACTIVITIES

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    Objective: To isolate and characterize novel actinomycetes and to evaluate their antibacterial activity against drug-resistant pathogenic bacteriaMethods: In the present study, 19 soil samples were collected from different localities of Ad-Dawadmi, Saudi Arabia. Actinomycetes were isolated from these samples using serial dilution and plating method on Actinomycetes isolation agar supplemented with nalidixic acid and actidione to inhibit bacteria and fungi. Crude extracts of potential actinomycetes were produced by submerged fermentation. The antimicrobial activity of crude extracts of actinomycetes was tested against different bacteria using the agar well diffusion method. Characterization of the isolates was done by morphological, physiological and biochemical methods.Results: A total of 9 (47%) isolates of actinomycetes were isolated from 19 different soil samples tested. Among them, 4 (44%) isolates confirmed as Streptomyces sp. showed potential antimicrobial activity against one or more test organisms. Crude extracts were made from these 4 actinomycetes isolates(DOM1, DOM3, DP3, DP4)and tested for their antibacterial activities against 4 different clinical bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Enterococcus). Crude extract from DP3 isolate showed highest antibacterial activity against all the four test organisms (28 mm, 21 mm, 20 mm and 18 mm) respectively and DP4 showed lowest antibacterial activity against all the four test organisms (14 mm, 12 mm, 0 mm, 6 mm) respectively. The highest zone of inhibition was shown by DP3 against Staphylococcus aureus (28 mm) and Escherichia coli was resistant for DP4. Most of the Inhibition zones produced by crude extracts showed significant differences when compared with control, tested against test organisms (P<0.05). Inhibition zones produced by DP3 and DOM1 against Staphylococcus aureus were 28 mm and 23 mm, respectively which were strong active when compared with control Ciprofloxacin (18 mm).Conclusion: Further studies for purification of bioactive metabolites and molecular characterization analysis of isolated Streptomyces sp. are in progress which would be helpful in discovering novel compounds of commercial value

    Targeted and untargeted metabolite profiling of the ethnobotanical Martynia annua L. identifies bioactive compounds with medicinal properties

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    Martynia annua is an indigenous plant found endemic in the Indian subcontinent where it is commonly used for self-treatment of a variety of ailments and diseases. Previous studies have shown that preparations from the plant have antiseptic, anti-inflammatory, and antiepileptic effects in vitro, but the biochemical composition and active compounds responsible for health benefits remain unknown. The aim of this study was to take extracts from different parts of the M. annua plant and, using targeted and untargeted metabolite profiling and quantitation, provide a comprehensive secondary metabolite profile to identify potential biotherapeutic metabolites. Ultrahigh-performance liquid chromatography, coupled directly to a Thermo Q-Exactive Orbitrap mass spectrometer, was used for high-resolution targeted and untargeted analysis. 89 metabolites were identified and their relative and selected absolute abundances measured across 5 different parts of the plant (leaf, flower, fruit, stem, and root). A number of the compounds identified are known to have bioactive and therapeutic properties; these include trans-ferulic acid, homovanillic acid, syringic acid, isorhamnetin, apigenin, luteolin, and hispidulin. We report their concentrations in different parts of the plant. Our findings significantly extend the plant metabolite profile of M. annua and amongst the compounds identified, we have highlight those with known biotherapeutic properties. These results provide a foundation for future studies addressing specific compounds that may be responsible for the bioactivity and therapeutic use of M. annua

    Anti-nociceptive, anti-inflammatory and antipyretic effects of the methanolic extract of Bombax buonopozense leaves in rats and mice

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    Methanolic extract of Bombax buonopozense was evaluated for possible anti-nociceptive, antiinflammatory and anti-pyretic activities in mice and rats. Acetic acid-induced abdominal constriction test in mice and formalin test in rats were used to investigate the antinociceptive effect of the extract. Studies were carried out on yeast-induced pyrexia and egg albumin-induced anti-inflammatory activity in rats. The extract produced a significant decrease in acetic acid-induced writhing in mice and inhibition of late phase of the formalin pain test in rats. The methanolic extract of B. buonopozense leaf also produced a potent antipyretic effect and significant inhibition of egg  albumin-induced antiinflammatory activity in rats. The result suggests that B. buonopozense contains biologically active substances with potential values for the treatment of fever, painful and inflammatory conditions.Keywords: Bombax buonopozense; analgesic, inflammation, pyrexia

    A prototype of an energy-efficient MAGLEV train : a step towards cleaner train transport

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    The magnetic levitation (MAGLEV) train uses magnetic field to suspend, guide, and propel vehicle onto the track. The MAGLEV train provides a sustainable and cleaner solution for train transportation by significantly reducing the energy usage and greenhouse gas emissions as compared to traditional train transportation systems. In this paper, we propose an advanced control mechanism using an Arduino microcontroller that selectively energizes the electromagnets in a MAGLEV train system to provide dynamic stability and energy efficiency. We also design the prototype of an energy-efficient MAGLEV train that leverages our proposed control mechanism. In our MAGLEV train prototype, the levitation is achieved by creating a repulsive magnetic field between the train and the track using magnets mounted on the top-side of the track and bottom-side of the vehicle. The propulsion is performed by creating a repulsive magnetic field between the permanent magnets attached on the sides of the vehicle and electromagnets mounted at the center of the track using electrodynamic suspension (EDS). The electromagnets are energized via a control mechanism that is applied through an Arduino microcontroller. The Arduino microcontroller is programmed in such a way to propel and guide the vehicle onto the track by appropriate switching of the electromagnets. We use an infrared-based remote-control device for controlling the power, speed, and direction of the vehicle in both the forward and the backward direction. The proposed MAGLEV train control mechanism is novel, and according to the best of our knowledge is the first study of its kind that uses an Arduino-based microcontroller system for control mechanism. Experimental results illustrate that the designed prototype consumes only 144 W-hour (Wh) of energy as compared to a conventionally designed MAGLEV train prototype that consumes 1200 Wh. Results reveal that our proposed control mechanism and prototype model can reduce the total power consumption by 8.3 x as compared to the traditional MAGLEV train prototype, and can be applied to practical MAGLEV trains with necessary modifications. Thus, our proposed prototype and control mechanism serves as a first step towards cleaner engineering of train transportation systems

    Social mining for sustainable cities: thematic study of gender-based violence coverage in news articles and domestic violence in relation to COVID-19

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    We argue that social computing and its diverse applications can contribute to the attainment of sustainable development goals (SDGs)—specifically to the SDGs concerning gender equality and empowerment of all women and girls, and to make cities and human settlements inclusive. To achieve the above goals for the sustainable growth of societies, it is crucial to study gender-based violence (GBV) in a smart city context, which is a common component of violence across socio-economic groups globally. This paper analyzes the nature of news articles reported in English newspapers of Pakistan, India, and the UK—accumulating 12,693 gender-based violence-related news articles. For the qualitative textual analysis, we employ Latent Dirichlet allocation for topic modeling and propose a Doc2Vec based word-embeddings model to classify gender-based violence-related content, called GBV2Vec. Further, by leveraging GBV2Vec, we also build an online tool that analyzes the sensitivity of Gender-based violence-related content from the textual data. We run a case study on GBV concerning COVID-19 by feeding the data collected through Google News API. Finally, we show different news reporting trends and the nature of the gender-based violence committed during the testing times of COVID-19. The approach and the toolkit that this paper proposes will be of great value to decision-makers and human rights activists, given the prompt and coordinated performance against gender-based violence in smart city context—and can contribute to the achievement of SDGs for sustainable growth of human societies

    A novel blood proteomic signature for prostate cancer

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    International audienceSimple Summary Despite intensive research, effective tools for detection and monitoring of prostate cancer remain to be found. Prostate-specific antigen (PSA), commonly used in prostate cancer assessments, can lead to overdiagnosis and overtreatment of indolent disease. This highlights the need for supporting non-invasive diagnostic, prognostic, and disease stratification biomarkers that could complement PSA in clinical decision-taking via increased sensitivity and specificity. In order to address this need, we uncover novel prostate cancer protein signatures by leveraging a cutting-edge analytical technique to measure proteins in patient samples. This strategy was used as a discovery tool to identify changes in protein levels in the serum of newly diagnosed patients as compared with healthy controls; the feature set was then further validated by reference to a second cohort of patients, achieving a high discriminatory ability. The proteomic maps generated also identified relevant changes in biological functions, notably the complement cascade. Prostate cancer is the most common malignant tumour in men. Improved testing for diagnosis, risk prediction, and response to treatment would improve care. Here, we identified a proteomic signature of prostate cancer in peripheral blood using data-independent acquisition mass spectrometry combined with machine learning. A highly predictive signature was derived, which was associated with relevant pathways, including the coagulation, complement, and clotting cascades, as well as plasma lipoprotein particle remodeling. We further validated the identified biomarkers against a second cohort, identifying a panel of five key markers (GP5, SERPINA5, ECM1, IGHG1, and THBS1) which retained most of the diagnostic power of the overall dataset, achieving an AUC of 0.91. Taken together, this study provides a proteomic signature complementary to PSA for the diagnosis of patients with localised prostate cancer, with the further potential for assessing risk of future development of prostate cancer. Data are available via ProteomeXchange with identifier PXD025484

    Transdermal oestradiol for androgen suppression in prostate cancer: long-term cardiovascular outcomes from the randomised Prostate Adenocarcinoma Transcutaneous Hormone (PATCH) trial programme

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    Background: Androgen suppression is a central component of prostate cancer management but causes substantial long-term toxicity. Transdermal administration of oestradiol (tE2) circumvents first-pass hepatic metabolism and, therefore, should avoid the cardiovascular toxicity seen with oral oestrogen and the oestrogen-depletion effects seen with luteinising hormone releasing hormone agonists (LHRHa). We present long-term cardiovascular follow-up data from the Prostate Adenocarcinoma Transcutaneous Hormone (PATCH) trial programme. Methods: PATCH is a seamless phase 2/3, randomised, multicentre trial programme at 52 study sites in the UK. Men with locally advanced or metastatic prostate cancer were randomly allocated (1:2 from August, 2007 then 1:1 from February, 2011) to either LHRHa according to local practice or tE2 patches (four 100 μg patches per 24 h, changed twice weekly, reducing to three patches twice weekly if castrate at 4 weeks [defined as testosterone ≤1·7 nmol/L]). Randomisation was done using a computer-based minimisation algorithm and was stratified by several factors, including disease stage, age, smoking status, and family history of cardiac disease. The primary outcome of this analysis was cardiovascular morbidity and mortality. Cardiovascular events, including heart failure, acute coronary syndrome, thromboembolic stroke, and other thromboembolic events, were confirmed using predefined criteria and source data. Sudden or unexpected deaths were attributed to a cardiovascular category if a confirmatory post-mortem report was available and as other relevant events if no post-mortem report was available. PATCH is registered with the ISRCTN registry, ISRCTN70406718; the study is ongoing and adaptive. Findings: Between Aug 14, 2007, and July 30, 2019, 1694 men were randomly allocated either LHRHa (n=790) or tE2 patches (n=904). Overall, median follow-up was 3·9 (IQR 2·4–7·0) years. Respective castration rates at 1 month and 3 months were 65% and 93% among patients assigned LHRHa and 83% and 93% among those allocated tE2. 157 events from 145 men met predefined cardiovascular criteria, with a further ten sudden deaths with no post-mortem report (total 167 events in 153 men). 26 (2%) of 1694 patients had fatal cardiovascular events, 15 (2%) of 790 assigned LHRHa and 11 (1%) of 904 allocated tE2. The time to first cardiovascular event did not differ between treatments (hazard ratio 1·11, 95% CI 0·80–1·53; p=0·54 [including sudden deaths without post-mortem report]; 1·20, 0·86–1·68; p=0·29 [confirmed group only]). 30 (34%) of 89 cardiovascular events in patients assigned tE2 occurred more than 3 months after tE2 was stopped or changed to LHRHa. The most frequent adverse events were gynaecomastia (all grades), with 279 (38%) events in 730 patients who received LHRHa versus 690 (86%) in 807 patients who received tE2 (p<0·0001) and hot flushes (all grades) in 628 (86%) of those who received LHRHa versus 280 (35%) who received tE2 (p<0·0001). Interpretation: Long-term data comparing tE2 patches with LHRHa show no evidence of a difference between treatments in cardiovascular mortality or morbidity. Oestrogens administered transdermally should be reconsidered for androgen suppression in the management of prostate cancer. Funding: Cancer Research UK, and Medical Research Council Clinical Trials Unit at University College London

    TNN-IDS: Transformer neural network-based intrusion detection system for MQTT-enabled IoT Networks

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    The Internet of Things (IoT) is a global network that connects a large number of smart devices. MQTT is a de facto standard, lightweight, and reliable protocol for machine-to-machine communication, widely adopted in IoT networks. Various smart devices within these networks are employed to handle sensitive information. However, the scale and openness of IoT networks make them highly vulnerable to security breaches and attacks, such as eavesdropping, weak authentication, and malicious payloads. Hence, there is a need for advanced machine learning (ML) and deep learning (DL)-based intrusion detection systems (IDS). Existing ML-based IoT-IDSs face several limitations in effectively detecting malicious activities, mainly due to imbalanced training data. To address this, this study introduces a transformer neural network-based intrusion detection system (TNN-IDS) specifically designed for MQTT-enabled IoT networks. The proposed approach aims to enhance the detection of malicious activities within these networks. The TNN-IDS leverages the parallel processing capability of the Transformer Neural Network, which accelerates the learning process and results in improved detection of malicious attacks. To evaluate the performance of the proposed system, it was compared with various IDSs based on ML and DL approaches. The experimental results demonstrate that the proposed TNN-IDS outperforms other systems in terms of detecting malicious activity. The TNN-IDS achieved optimum accuracies reaching 99.9% in detecting malicious activities

    Real world, multicentre patterns of treatment and survival in metastatic renal cell carcinoma with the UK Renal Oncology Collaborative (UK ROC): Is it time to look favourably on first-line immunotherapy containing combinations in all IMDC groups?

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    \ua9 2024 The Author(s). Cancer Medicine published by John Wiley &amp; Sons Ltd.Introduction: Clinical trials show improved progression-free survival (PFS) and overall survival (OS) in first-line metastatic renal cell carcinoma (mRCC) patients with immunotherapy containing systemic anti-cancer therapies (SACT). However, in the favourable international metastatic renal cell cancer database consortium (IMDC) group there is no trial evidence for OS benefit despite clear PFS improvement when comparing anti-VEGF tyrosine kinase inhibitor (TKI) monotherapy and (immunotherapy and TKI) IO/TKI combinations. Objective: To assess the impact of first-line SACT choice on the clinical outcomes of PFS and OS in mRCC. To evaluate this impact of initial SACT for allcomers and the favourable IMDC group. Methods: A multicentre retrospective review of patients who started SACT for mRCC (01/01/2018–30/06/2021) at 17 UK NHS trusts. Patient demographics and IMDC group were analysed. Survival data were compared using Kaplan–Meier curves, and the statistical significance of differences in outcome between the groups was assessed with the log-rank test. Univariable and multivariable Cox proportional hazard modelling estimate the hazard ratios (HRs) for survival outcomes associated with IMDC and treatment subtype. Results: One thousand three hundred and nineteen patients were identified with a median age of 64. 294 (22.3%), 695 (52.7%) and 321 (24.3%) were IMDC group favourable, intermediate and poor, respectively. 311 (23.6%), 197 (14.9%) and 778 (59%) patients received checkpoint inhibitor and anti-CTLA4 monoclonal antibody (IO/IO), IO/TKI and TKI first-line SACT across all IMDC groups. Significant PFS improvement favouring IO/TKI versus TKI was demonstrated in allcomers HR = 0.61. In the favourable risk group, Log rank testing demonstrated a significant benefit for IO/TKI over TKI for PFS (HR = 0.60, 95% CI [0.39, 0.91]) and OS (HR = 0.42, 95% CI [0.18, 0.99]). Conclusion: In this real-world evidence cohort, we have shown OS and PFS benefit with IO/TKI versus TKI in the favourable IMDC risk group. This has not been previously reported from trial outcomes and would support use of front-line IO/TKI in mRCC favourable risk patients
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