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1.
Sensors (Basel) ; 23(18)2023 Sep 08.
Artigo em Inglês | MEDLINE | ID: mdl-37765819

RESUMO

The reliable and safe operation of industrial systems needs to detect and diagnose bearing faults as early as possible. Intelligent fault diagnostic systems that use deep learning convolutional neural network (CNN) techniques have achieved a great deal of success in recent years. In a traditional CNN, the fully connected layer is located in the final three layers, and such a layer consists of multiple layers that are all connected. However, the fully connected layer of the CNN has the disadvantage of too many training parameters, which makes the model training and testing time longer and incurs overfitting. Additionally, because the working load is constantly changing and noise from the place of operation is unavoidable, the efficiency of intelligent fault diagnosis techniques suffers great reductions. In this research, we propose a novel technique that can effectively solve the problem of traditional CNN and accurately identify the bearing fault. Firstly, the best pre-trained CNN model is identified by considering the classification's success rate for bearing fault diagnosis. Secondly, the selected CNN model is modified to effectively reduce the parameter quantities, overfitting, and calculating time of this model. Finally, the best classifier is identified to make a hybrid model concept to achieve the best performance. It is found that the proposed technique performs well under different load conditions, even in noisy environments, with variable signal-to-noise ratio (SNR) values. Our experimental results confirm that this proposed method is highly reliable and efficient in detecting and classifying bearing faults.

2.
Sensors (Basel) ; 20(9)2020 Apr 29.
Artigo em Inglês | MEDLINE | ID: mdl-32365610

RESUMO

Spectrum sensing plays a vital role in cognitive radio networks (CRNs) for identifying the spectrum hole. However, an individual cognitive radio user in a CRN does not obtain sufficient sensing performance and sum rate of the primary and secondary links to support the future Internet of Things (IoT) using conventional detection techniques such as the energy detection (ED) technique in a noise-uncertain environment. In an environment comprising noise uncertainty, the performance of conventional energy detection techniques is significantly degraded owing to the noise fluctuation caused by the noise temperature, interference, and filtering. To mitigate this problem, we present a cooperative spectrum sensing technique that comprises the use of the Kullback-Leibler divergence (KLD) in cognitive radio-based IoT (CR-IoT). In the proposed method, each unlicensed IoT device that is capable of spectrum sensing, which is called a CR-IoT user, makes a local decision using the KLD technique. The spectrum sensing performed with the KLD requires a smaller number of samples than other conventional approaches, e.g., energy detection, for reliable sensing even in a noise uncertain environment. After the local decision is made, each CR-IoT user sends its own local decision result to the corresponding fusion center, which makes a global decision using the soft fusion rule. The results obtained through simulations show that the proposed KLD scheme achieves a better sensing performance, i.e., higher detection and lower false-alarm probabilities, enhances the sum rate, and reduces the total time as compared to the conventional ED scheme under various fading channels.

3.
Sci Rep ; 14(1): 22797, 2024 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-39354009

RESUMO

Brain tumor, a leading cause of uncontrolled cell growth in the central nervous system, presents substantial challenges in medical diagnosis and treatment. Early and accurate detection is essential for effective intervention. This study aims to enhance the detection and classification of brain tumors in Magnetic Resonance Imaging (MRI) scans using an innovative framework combining Vision Transformer (ViT) and Gated Recurrent Unit (GRU) models. We utilized primary MRI data from Bangabandhu Sheikh Mujib Medical College Hospital (BSMMCH) in Faridpur, Bangladesh. Our hybrid ViT-GRU model extracts essential features via ViT and identifies relationships between these features using GRU, addressing class imbalance and outperforming existing diagnostic methods. We extensively processed the dataset, and then trained the model using various optimizers (SGD, Adam, AdamW) and evaluated through rigorous 10-fold cross-validation. Additionally, we incorporated Explainable Artificial Intelligence (XAI) techniques-Attention Map, SHAP, and LIME-to enhance the interpretability of the model's predictions. For the primary dataset BrTMHD-2023, the ViT-GRU model achieved precision, recall, and F1-score metrics of 97%. The highest accuracies obtained with SGD, Adam, and AdamW optimizers were 81.66%, 96.56%, and 98.97%, respectively. Our model outperformed existing Transfer Learning models by 1.26%, as validated through comparative analysis and cross-validation. The proposed model also shows excellent performances with another Brain Tumor Kaggle Dataset outperforming the existing research done on the same dataset with 96.08% accuracy. The proposed ViT-GRU framework significantly improves the detection and classification of brain tumors in MRI scans. The integration of XAI techniques enhances the model's transparency and reliability, fostering trust among clinicians and facilitating clinical application. Future work will expand the dataset and apply findings to real-time diagnostic devices, advancing the field.


Assuntos
Neoplasias Encefálicas , Imageamento por Ressonância Magnética , Humanos , Bangladesh , Imageamento por Ressonância Magnética/métodos , Neoplasias Encefálicas/diagnóstico por imagem , Neoplasias Encefálicas/classificação , Neoplasias Encefálicas/patologia , Inteligência Artificial , Algoritmos , Interpretação de Imagem Assistida por Computador/métodos
4.
Life Sci ; 297: 120483, 2022 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-35288173

RESUMO

AIMS: Due to traditional endocrinological techniques, there is currently no shared work available, and no therapeutic choices have been presented in type 2 diabetes (T2D), rheumatoid arthritis (RA), and tuberculosis (TB). The purpose of this research is to summarize the prospective molecular complications and potential therapeutic targets associated with T2D that have been connected to the development of TB and RA. MATERIALS AND METHODS: We collected the transcriptomic data as GSE92724, GSE110999 and GSE 148036 for T2D, RA and TB patients. After collecting from NCBI, then GREIN were employed to process our datasets. STRING and Enrichr were used to construct protein-protein interaction (PPI), gene regulatory network (GRN), protein-drug-chemical, gene ontology and pathway network. Finally, Cytoscape and R studio were employed to visualize our proposed network. KEY FINDINGS: We discovered a number of strong candidate hub proteins in significant pathways, namely RAB25, MAL2, SFN, MYO5B, and HLA-DQB1 out of 75 common genes. We also identified a number of TFs (JUN, TFAP2A, FOXC1, and GATA2); miRNA (mir-1-3p, mir-16-5p, and mir-34a5p); drugs (sulfasalazine, cholic acid, and nilflumic acid) and chemicals (Valproic acid, and Aflatoxin B1) may control DEGs in transcription as well as post- transcriptional expression levels. SIGNIFICANCE: To summarize, our computational techniques discovered unique potential biomarkers that show how T2D, RA, and TB interacted, as well as pathways and gene regulators by which T2D may influence autoimmune inflammation and infectious diseases. In the future, more clinical and pharmacological research is needed to confirm the findings at the transcriptional and translational levels.


Assuntos
Artrite Reumatoide , Diabetes Mellitus Tipo 2 , Tuberculose , Artrite Reumatoide/tratamento farmacológico , Artrite Reumatoide/genética , Artrite Reumatoide/metabolismo , Diabetes Mellitus Tipo 2/genética , Ontologia Genética , Humanos , Proteínas Proteolipídicas Associadas a Linfócitos e Mielina/metabolismo , Estudos Prospectivos , Tuberculose/tratamento farmacológico , Tuberculose/genética , Proteínas rab de Ligação ao GTP/metabolismo
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