Browse Items (11810 total)
Sort by:
-
Predictive analytics for cardiac arrhythmia using machine intelligence
Myocardial Infarction (MI) is the primary cause of death worldwide. MI occurs when a plaque buildup in the inner surface of the coronary artery suddenly ruptures and prevents the blood flow. A heart attack is medically termed as MI. It is the irreversible damage caused by the prolonged ischemia. Ischemia is nothing but the heart organ doesn’t get enough blood and oxygen which is also termed as coronary artery disease or coronary
heart disease. The heart gets damaged if it has not received enough blood or oxygen. In connection to the damage of the heart, arrhythmia would occur. Arrhythmia is the problem based on the heart rhythm or rate of the heartbeat. Tachycardia, when there is a fast beat in the heart. Bradycardia, when the heart beats too slow. The common type of arrhythmia is atrial fibrillation. The great concern is that the patient who has arrhythmia has to be treated immediately. They lose consciousness in a few minutes when the heart is not pumping enough blood mainly to the brain. Death occurs when the patient is not given emergency treatment. -
Predictive analytics for cardiac arrhythmia using machine intelligence
Myocardial Infarction (MI) is the primary cause of death worldwide. MI occurs when a plaque buildup in the inner surface of the coronary artery suddenly ruptures and prevents the blood flow. A heart attack is medically termed as MI. It is the irreversible damage caused by the prolonged ischemia. Ischemia is nothing but the heart organ doesn t get enough blood and oxygen which is also termed as coronary artery disease or coronary heart disease. The heart gets damaged if it has not received enough blood or oxygen. In connection to the damage of the heart, arrhythmia would occur. Arrhythmia is the problem based on the heart rhythm or rate of the heartbeat. Tachycardia, when there is a fast beat in the heart. Bradycardia, when the heart beats too slow. The common type of arrhythmia is atrial fibrillation. The great concern is that the patient who has arrhythmia has to be treated immediately. They lose consciousness in a few minutes when the heart is not pumping enough blood mainly to the brain. Death occurs when the patient is not given emergency treatment. newline Treatment which is included in the emergency is defibrillation and Cardiopulmonary Resuscitation (CPR). CPR is an emergency procedure which is combined with the chest compressions. It is through artificial ventilation which gives manual effort, preserves the brain functions until further treatment for the restoration of spontaneous blood circulation. The common symptoms of sudden cardiac death are chest pain, shortness of breath, severe wheezing, irregular heartbeats, fainting etc. newlineHeart Scar tissue which is not like heart muscle. It doesn t contrast like the normal heart muscle. Heart muscles get damaged for the heart attack patient based on the time of the treatment. The damage of the heart is based on the blockage of the artery. Arrhythmia can be predicted based on the volume of the scar region in the heart. Arrhythmia patients are treated by fixing Implantable Cardioverter Defibrillator (ICD). -
A Study on defective colouring of graphs
If different technology represents distinct colours that are to be located on some geographical region which can be represented as vertices of a graph, then the proper colouring is obtained when no two technology of same type share a common edge between the vertices they are placed on. The minimum number of technology required for such a colouring of a graph is the chromatic number of the graph. However, if the available technology are less than that of the minimum required, then the question arises on how to place the technology on the vertices of a graph in such a way that there is a minimum adjacency between the technology of same type. The solution for this problem can be attained by defining certain rules for the properness of colouring in which a few thresholds are tolerated. We know that, in a proper colouring every colour class is an independent set. If the available colours to colour a graph is less than that of the chromatic number of graphs, then a threshold that can be tolerated is permitting few colour classes to be non-independent set. An edge uv is said to be a monochromatic edge or bad edge if the colours assigned to both u and v are the same. A near proper colouring of graphs is a colouring that minimises the number of monochromatic edges by permitting few colour classes to have adjacency between the elements in it. The minimum number of monochromatic edges obtained from near proper colouring is called near defect number, denoted by B_k (G). A and#948;^((k))-colouring of graph G is a near proper colouring of G consisting of k given colours, where 1and#8804;kand#8804;and#967;(G)-1, which minimises the number of monochromatic edges by permitting at most one colour class to have adjacency among the vertices in it. The and#948;^((k))-defect number is the minimum number of monochromatic edges obtained from a and#948;^((k))-colouring of graphs and it is denoted by b_k(G). The study concerned is the further work on a near proper colouring and a and#948;^((k))-colouring of graphs. -
Harnessing transition metal oxide?carbon heterostructures: Pioneering electrocatalysts for energy systems and other applications
Exponential demand for energy resources and fossil fuel substitution with green alternatives are essential to bringing sustainable development and a solution to the energy crisis. Transition metal oxides (TMOs) and their composites (TMOCs) as promising electrocatalysts to develop potential energy conversion and storage devices contribute to the solution to this crisis. The productivity of green fuels such as hydrogen from water-splitting reactions, the efficiency of energy storage and harvesting devices including supercapacitors and batteries, and the performance of electrochemical sensors can be remarkably enhanced with TMOs and their composites. Excellent electrochemical attributes, stability, abundant reserves, low cost, environment-friendly, and low toxicity make TMOs and their composites an excellent choice. The tunability of the physical and chemical properties of TMOs makes them attractive for research in designing different energy storage devices. This review presents a concise overview of the unique physical and electrochemical aspects of various TMOs and TMOCs, such as spinels, perovskites, and TMO-integrated carbon-based compounds, and their relevance for specific applications, emphasizing energy-related fields. The recent research advancements of TMOs-based functional materials for emerging applications, such as water splitting, fuel cells, supercapacitors, batteries, and sensing, are discussed. This review also highlights the advantageous properties and pertinent fabrication methods of TMOs and TMOCs for electrocatalysis, along with the methods to enhance their electrocatalytic abilities, which improve the overall efficiency of the desired applications. 2024 -
Discovery of inverse-Compton X-ray emission and estimate of the volume-averaged magnetic field in a galaxy group
Observed in a significant fraction of clusters and groups of galaxies, diffuse radio synchrotron emission reveals the presence of relativistic electrons and magnetic fields permeating large scale systems of galaxies. Although, these non-thermal electrons are expected to upscatter cosmic microwave background photons up to hard X-ray energies, such inverse-Compton (IC) X-ray emission has so far not been unambiguously detected on cluster/group scales. Using deep, new proprietary XMM-Newton observations (?200 ks of clean exposure), we report a 4.6 ? detection of extended IC X-ray emission in MRC 0116 +111, an extraordinary group of galaxies at z = 0.131. Assuming a spectral slope derived from low frequency radio data, the detection remains robust to systematic uncertainties. Together with low frequency radio data from the Giant Metrewave Radio Telescope (GMRT), this detection provides an estimate for the volume-averaged magnetic field of (1.9 0.3) ?G within the central part of the group. This value can serve as an anchor for studies of magnetic fields in the largest gravitationally bound systems in the Universe. 2023 The Author(s) Published by Oxford University Press on behalf of Royal Astronomical Society. -
FSDA: Framework for Secure Data Aggregation in wireless sensor network for enhancing key management
An effective key management plays a crucial role in imposing a resilient security technique in Wireless Sensor Network (WSN). After reviewing the existing approaches of key management, it is confirmed that existing approachs does not offer good coverage on all potential security breaches in WSN. With WSN being essential part of Internet-of-Things (IoT), the existing approaches of key management can definitely not address such security breaches. Therefore, this paper introduces a Framework for Secure Data Aggregation (FSDA) that hybridizes the public key encryption mechanism in order to obtain a novel key management system. The proposed system does not target any specific attacks but is widely applicable for both internal and external attacks in WSN owing to its design principle. The study outcome exhibits that proposed FSDA offers highly reduced computational burden, minimal delay, less energy consumption, and higher data transmission perforance in contrast to frequency used encryption schemes in WSN. Copyright 2018 Institute of Advanced Engineering and Science. All rights reserved. -
N-tier modelling of robust key management for secure data aggregation in wireless sensor network
Security problems in Wireless Sensor Network (WSN) have been researched from more than a decade. There are various security approaches being evolving towards resisting various forms of attack using different methodologies. After reviewing the existing security approaches, it can be concluded that such security approaches are highly attack-specific and doesnt address various associated issues in WSN. It is essential for security approach to be computationally lightweight. Therefore, this paper presents a novel analytical modelling that is based on n-tier approach with a target to generate an optimized secret key that could ensure higher degree of security during the process of data aggregation in WSN. The study outcome shows that proposed system is computationally lightweight with good performance on reduced delay and reduced energy consumption. It also exhibits enhanced response time and good data delivery performance to balance the need of security and data forwarding performance in WSN. 2019 Institute of Advanced Engineering and Science. -
RASK: Request authentication using shared keys for secured data aggregation in sensor network
Accomplishing a robust security features to resists lethal attacks is still an open research area in wireless sensor network. The present paper review existing security techniques to find that there is still a trade-off between cryptographic-based security incorporations and communication performance. Moreover, we have identified that majority of the existing system has not emphasized on first line of defense i.e. security the route discovery process that can act as a firewall for all forms of illegitimate nodes existing in the network. The proposed study introduced RASK i.e. Request Authentication using Shared Key, which is a novel concept developed using simple quadratic formulation of generating keys for encrypting the message during data aggregation. The study outcome has been significantly benchmarked with recent studies and existing cryptographic standards to find RASK outperform existing techniques. Springer International Publishing AG 2017. -
A genome wide association study of fast beta EEG in families of European ancestry
Background Differences in fast beta (2028Hz) electroencephalogram (EEG) oscillatory activity distinguish some individuals with psychiatric and substance use disorders, suggesting that it may be a useful endophenotype for studying the genetics of disorders characterized by neural hyper-excitability. Despite the high heritability estimates provided by twin and family studies, there have been relatively few genetic studies of beta EEG, and to date only one genetic association finding has replicated (i.e., GABRA2). Method In a sample of 1564 individuals from 117 families of European Ancestry (EA) drawn from the Collaborative Study on the Genetics of Alcoholism (COGA), we performed a Genome-Wide Association Study (GWAS) on resting-state fronto-central fast beta EEG power, adjusting regression models for family relatedness, age, sex, and ancestry. To further characterize genetic findings, we examined the functional and behavioral significance of GWAS findings. Results Three intronic variants located within DSE (dermatan sulfate epimerase) on 6q22 were associated with fast beta EEG at a genome wide significant level (p<5נ10?8). The most significant SNP was rs2252790 (p<2.6נ10?8; MAF=0.36; ?=0.135). rs2252790 is an eQTL for ROS1 expressed most robustly in the temporal cortex (p=1.2נ10?6) and for DSE/TSPYL4 expressed most robustly in the hippocampus (p=7.3נ10?4; ?=0.29). Previous studies have indicated that DSE is involved in a network of genes integral to membrane organization; gene-based tests indicated that several variants within this network (i.e., DSE, ZEB2, RND3, MCTP1, and CTBP2) were also associated with beta EEG (empirical p<0.05), and of these genes, ZEB2 and CTBP2 were associated with DSM-V Alcohol Use Disorder (AUD; empirical p<0.05). Discussion In this sample of EA families enriched for AUDs, fast beta EEG is associated with variants within DSE on 6q22; the most significant SNP influences the mRNA expression of DSE and ROS1 in hippocampus and temporal cortex, brain regions important for beta EEG activity. Gene-based tests suggest evidence of association with related genes, ZEB2, RND3, MCTP1, CTBP2, and beta EEG. Converging data from GWAS, gene expression, and gene-networks presented in this study provide support for the role of genetic variants within DSE and related genes in neural hyperexcitability, and has highlighted two potential candidate genes for AUD and/or related neurological conditions: ZEB2 and CTBP2. However, results must be replicated in large, independent samples. 2016 Elsevier B.V. -
Genetic and cytogenetic screening of autistic spectrum disorder: Genotype-phenotype profiles
Autism, a pervasive developmental disorder typically characterized by repetitive behaviour, social skills deficit (or a deficit in social communication), speech and language impairments. Our prime focus is to analyze the clinical features and phenotypical behavioural changes using the diagnostic and statistical manual of mental disorders, fourth edition, text revision (DSM IV-TR), and locating the biomarkers associated with specific autistic characters using karyotyping and fluorescence in situ hybridization (FISH) techniques. The prevalence rate of the neurexin 1 (NRXN1) gene polymorphism was also assessed in the current study. The study group involved 196 samples with 98 autistics, and equal age-matched (2) controls based on their birth order and carrier. The participants include 35.2% males (n = 69) and 14.8% females (n = 29). The autistic and control participants were categorized based on their ages as group I (<12 yrs) with n = 62; males n = 41 (20.9%); females n = 21 (10.7%) and group II (?12 yrs)-n = 36; males n = 28 (14.2%); females n = 08 (4.08%). Karyotyping was done for autism participants (n = 98) and the results showed that 90% of autistic participants were either the only child or the first child with a low perception and frequency in both the groups. Subsequently, we carried out the FISH assay on participants (n = 37) with higher DSM-IV TR score (?30). Only 30 FISH tests were negative for subtelomeric deletions with NRXN1 polymorphism genotypic frequency as 62.50%, 25% and 25% for A/A, A/G and G/G genotype respectively. Our study suggests the link between a haplotype with clinical signs of autism for the single nucleotide sequence (SNP rs9636391) and links autistic characters and gene among autistic children according to their birth order, age and gender in India. 2021 Elsevier B.V. -
Biomarker study of the biological parameter and neurotransmitter levels in autistics
Autism is a prevalent developmental disorder that combines repetitive behaviours, social deficits and language abnormalities. The present study aims to assess the autistic subjects using DSM IV-TR criteria followed with the analysis of neurotransmitters, biochemical parameters, oxidative stress and its ions in two groups of autistic subjects (group I < 12years; group II ? 12years). Antioxidants show a variation of 10% increase in controls compared to autistic age < 12years. The concentration of pyruvate kinase and hexokinase is elevated in controls approximately 60% and 45%, respectively, with the significance of 95 and 99%. Autistic subjects showed marked variation in levels of neurotransmitters, oxidative stress and its related ions. Cumulative assessment of parameters related to biochemical markers and neurotransmitters paves the way for autism-based research, although these observations draw interest in an integrated approach for autism. 2020, Springer Science+Business Media, LLC, part of Springer Nature. -
Crux role of neurocomputing in teaching learning pedagogy
The advent of brain-based learning in the early 1990s has limelighted the syndication between the educational learning process and neurosciences. Through educational learning ability, an individual can gather and assimilate anecdotes or come up with new notions with logical conclusions to form an organizational memory. Supreme level of knowledge assimilation ability results in developing new crucial knowledge for strategic renewal for the betterment of the learning process. Earlier efforts to link neuroscience and learning mode were controversial. However, continuous researches imply the significant role of neurosciences in the field of education and its deep-rooted involvement in building reformed educational pedagogy related to curriculum and general teaching-learning practices. Educational neurosciences help in interpreting brain-behaviour intricacy to provide latest teaching-learning strategies. Education is the most robust cognitive skill developer, and it must be provided to all irrespective of age and gender as it makes the person flexible and provides strength to cope with the adversities. Through this report, we would like to covey the deep association between the teaching-learning process with neurological sciences along with providing measures to be taken for holistic development in the educational setups. Learning is a by-product of human behaviour towards the external environment. Recent advanced tools of neuroimaging aid in more in-depth insight linked to adaptive neural mechanics, knowledge attainment, new skill acquisition and building neuroscience network for human learning. The neuroscience research shows intricacy between emotions and cognition as mediators between mind and body that are then followed by the social behaviour and learning, by indulging in subjective interpretations of person's goals, feelings, actions and experiences, ultimately resulting in learning new theories through neurobiological shreds of evidence. The Author(s), under exclusive license to Springer Nature Switzerland AG 2021. All rights reserved. -
Clinical implications of chromosomal polymorphisms in congenital disorders
Alterations in the DNA sequence are generally seen in the general population at >1%, and these alterations can be deletions or insertions. Classically, chromosomal polymorphisms (CPMs) are alterations with no significant phenotypic distinctions. However, few studies have shown that the presence of CPM can lead to congenital disabilities, which can be fatal. These variants in the DNA can happen in the form of single nucleotide polymorphisms (SNPs). The human genome is considered full of SNPs, and they are responsible for causing pathological phenotypes and provide insight into pathogenesis, a therapeutic approach to the pathology. About 100 million SNPs are observed in humans for an average of 300 nucleotides. These polymorphisms are detected by using molecular techniques. These polymorphisms are not just restricted to the coding region. The CPMs are first recognized on the chromosomes through molecular techniques, followed by detection of the polymorphism. The CMPs are generally the SNPs, deletions/duplications, and presence of microsatellite DNAs. Here we have summarized the implications of CMPs in a few congenital disorders and the method of diagnosis. The Author(s), under exclusive license to Springer Nature Switzerland AG 2023. -
The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment
Inherited neurodegenerative pathology characterized by lower muscle tone and increasing spasticity in the lower limbs is termed hereditary spastic paraplegia (HSP). HSP is associated with changes in about 80 genes and their products involved in various biochemical pathways, such as lipid droplet formation, endoplasmic reticulum shaping, axon transport, endosome trafficking, and mitochondrial function. With the inheritance patterns of autosomal dominant, autosomal recessive, X-linked recessive, and mitochondrial inheritance, HSP is prevalent around the globe at a rate of 15 cases in every 100,000 individuals. Recent technology and medical interventions somewhat aid in recognizing and managing the malaise. However, HSP still lacks an appropriate and adequate therapeutic approach. Current therapies are based on the clinical manifestations observed in the patients, for example, smoothing the relaxant spastic muscle and physiotherapies. The limited clinical trial studies contribute to the absence of specific pharmaceuticals for HSPs. Our current work briefly explains the causative genes, epidemiology, underlying mechanism, and the management approach undertaken to date. We have also mentioned the latest approved drugs to summarise the available knowledge on therapeutic strategies for HSP. 2022 by the authors. -
Cytokine see-saw across pregnancy, its related complexities and consequences
During pregnancy, a woman's immune system adapts to the changing hormonal concentrations, causing immunologic transition. These immunologic changes are required for a full-term pregnancy, preserving the fetus' innate and adaptive immunity. Preterm labor, miscarriage, gestational diabetes mellitus, and pre-eclampsia are all caused by abnormal cytokine expression during pregnancy and childbirth. A disruption in the cytokine balance can lead to autoimmune diseases or microbiologic infections, or to autoimmune illness remission during pregnancy with postpartum recurrence. The cytokine treatments are essential and damaging to the developing fetus. The current review summarizes the known research on cytokine changes during pregnancy and their possible consequences for pregnant women. Studies suggest that customizing medication for each woman and her progesterone levels should be based on the cytokine profile of each pregnant woman. Immune cells and chemicals play an important function in development of the placenta and embryo. During pregnancy, T cells divide and move, and a careful balance between proinflammatory and anti-inflammatory cytokines is necessary. The present review focuses on the mother's endurance in generating fetal cells and the immunologic mechanism involved. 2022 International Federation of Gynecology and Obstetrics. -
Nutrition paves the way to environmental toxicants and influences fetal development during pregnancy
Nutrition plays a major role in the healthy pregnancy and development of the fetus. In addition, nutrition can expose humans to a wide range of potentially hazardous environmental constituents, such as organic pollutants and heavy metals from marine or agricultural food products while processing, producing, and packaging. Humans constantly face these constituents through air, water, soil, food, and domestic products. During pregnancy, the rate of cellular division and differentiation is higher; exposure to any of these environmental toxicants can lead to developmental defects as they cross the placental barrier and, in some cases, can harm the successive generation too, as some contaminants can act on the reproductive cells of the fetus (Diethylstilbestrol). Pregnant women are considered a vulnerable population to food contaminant exposure and require a proper dietary chart and conscious food choices. Food is a source of both essential nutrients and environmental toxicants. Here, we have researched the possible toxicants of the food industry and their influence on the fetus's in-utero development, along with the importance of dietary interventions and the need to balance a healthy diet to overcome the harms. The cumulative exposure to environmental toxicants can influence the mother's prenatal environment and affect the fetus's development. 2023 -
Customary complications and screening techniques of early pregnancy
Complications arising during pregnancy are one of the significant public health issues around the world. Being the critical aspect for the growth and development in every human's life, it is necessary to assess any pathological disturbance mainly concerning the well-being of the fetus and mother throughout pregnancy. Few women face health downline while pregnancy, whereas few faces before getting pregnant; both the conditions can lead to complications in maternal and fetal health. Usually, pregnancy-related complications disappear as soon as the baby is delivered or shortly after that. Few complications include premature delivery, abruption of the placenta, preeclampsia, and diabetes. At the same time, gestation and these complications reoccur in successive pregnancies at a higher rate. They can also make the women prone to lifelong medical complications such as metabolic diseases or cardiovascular disease later in life. Most of the complications are mild without progression, but it harms both the mother and baby when they progress. Hence, it is important to diagnose early the danger signs and provide antenatal care to elevate the chances of proper health in both the mother and infant throughout the pregnancy and afterwards. This chapter focuses on the complications faced in the early phase of pregnancies and the screening methods utilized to diagnose them early, along with long-term effects in mothers due to some complications. The Author(s), under exclusive license to Springer Nature Switzerland AG 2023. -
COVID-19 in pregnant women and children: Insights on clinical manifestations, complexities, and pathogenesis
Pregnancy changes the body's immune system to counteract the spectrum of infections, including COVID-19, which can pose complications. Pregnant women are less likely to contract COVID-19 infections than the general public. However, pregnant women are at slightly increased risk of becoming severely unwell if they do catch COVID-19, and congenital conditions in pregnant women may worsen the state of infection and lead to critical stages and even mortality. The possibility of vertical transmission has been reported in only a few cases of COVID-19; however, it was not noted in cases of SARS and MERS. Vaccination coverage in pregnant women remains a challenge. Children are the next suspected and vulnerable population to acquire infection after the first and second waves. Children are disproportionately infected compared with older populations, but the severity of infection is less compared to adults. This review highlights the complexities of COVID-19 in pregnant women and the underlying reasons why children tend to be comparatively less severely affected. Ethnicity, nutrition, lifestyle, and therapeutics influence the severity of infection in children. Low expression of angiotensin-converting enzyme 2 receptors, indigenous virus competence, and maternal immunity is the first-line defense for children against COVID-19. Habituating herbal medicines from childhood may help support a robust and defensive immune system to counteract novel antigens and encourage healthy generations. 2021 International Federation of Gynecology and Obstetrics -
A Bose horn antenna radio telescope (BHARAT) design for 21 cm hydrogen line experiments for radio astronomy teaching
We have designed a low-cost radio telescope system named the Bose Horn Antenna Radio Telescope (BHARAT) to detect the 21 cm hydrogen line emission from our Galaxy. The system is being used at the Radio Physics Laboratory (RPL) (Radio Physics Lab, IUCAA NCRA-TIFR, , ), Inter-University Centre for Astronomy and Astrophysics (IUCAA), India, for laboratory sessions and training students and teachers. It is also a part of the laboratory curriculum at several universities and colleges. Here, we present the design of a highly efficient, easy to build, and cost-effective dual-mode conical horn used as a radio telescope and describe the calibration procedure. We also present some model observation data acquired using the telescope for facilitating easy incorporation of this experiment in the laboratory curriculum of undergraduate or post-graduate programs. We have named the antenna after Acharya (teacher or an influential mentor) Jagadish Chandra Bose, honoring a pioneer in radio-wave science and an outstanding teacher, who inspired several world renowned scientists. 2022 Author(s). -
Efficiency Wage and Productivity in the Indian Microfinance Industry: A Panel Evidence
Enhanced productivity remains a crucial agenda for firms to attain cost and competitive advantages in the market. Hence, the main purpose of this study is to investigate the effects of efficiency wage (EW) on the productivity of microfinance institutions (MFIs) with respect to their dual objectives, namely, outreach (depth and breadth) and financial sustainability. Unbalanced panel data of 179 Indian MFIs were collected over the period 20102018 from the Microfinance Information Exchange (MIX) market platform (now obtainable from the World Bank catalogue). Under a static model setting (fixed effects model), the observed relationship between EW and MFIs productivity is mixed. On the one hand, EW exhibits a strong and statistically significant positive relationship with the breadth of outreach, even after considering various control variables and alternative proxies of EW. On the other hand, EW shows no positive influence on the MFIs depth of outreach; rather, it results in a mission drift of MFIs, with the poorest of the poor being neglected (weak and insignificant for proxy of EW). Concerning the financial sustainability of MFIs, EW exhibits a positive and statistically significant effect, except for the profitability dimension when an alternative proxy of EW is used. A two-step system generalized method of moments (GMM) performed to limit endogeneity problems also validates most of our findings. The outcomes of this study could help MFIs managers in designing appropriate financial packages to enhance MFIs productivity and subsequently attain the dual objective of outreach and sustainability. 2022 SAGE Publications.