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1.
Artigo em Inglês | MEDLINE | ID: mdl-38607744

RESUMO

The purpose of this work is to analyze how new technologies can enhance clinical practice while also examining the physical traits of emotional expressiveness of face expression in a number of psychiatric illnesses. Hence, in this work, an automatic facial expression recognition system has been proposed that analyzes static, sequential, or video facial images from medical healthcare data to detect emotions in people's facial regions. The proposed method has been implemented in five steps. The first step is image preprocessing, where a facial region of interest has been segmented from the input image. The second component includes a classical deep feature representation and the quantum part that involves successive sets of quantum convolutional layers followed by random quantum variational circuits for feature learning. Here, the proposed system has attained a faster training approach using the proposed quantum convolutional neural network approach that takes [Formula: see text] time. In contrast, the classical convolutional neural network models have [Formula: see text] time. Additionally, some performance improvement techniques, such as image augmentation, fine-tuning, matrix normalization, and transfer learning methods, have been applied to the recognition system. Finally, the scores due to classical and quantum deep learning models are fused to improve the performance of the proposed method. Extensive experimentation with Karolinska-directed emotional faces (KDEF), Static Facial Expressions in the Wild (SFEW 2.0), and Facial Expression Recognition 2013 (FER-2013) benchmark databases and compared with other state-of-the-art methods that show the improvement of the proposed system.


Assuntos
Reconhecimento Facial , Saúde Mental , Humanos , Benchmarking , Bases de Dados Factuais , Redes Neurais de Computação
2.
Artigo em Inglês | MEDLINE | ID: mdl-38424698

RESUMO

Even though many different approaches have been employed to address the complex mutational heterogeneity of cancer, finding driver genes is still problematic since other genomic factors cannot be fully integrated for combined analyses. This research paper presents a novel gene identification and segregation model with five key processes (a) pre-processing, (b) treatment of class imbalances, (c) feature extraction, (d) feature selection, and (e) gene classification. To increase the data quality, the gathered initial information is first pre-processed utilizing data cleaning and data normalization. This turns the raw data into something that is both useful and effective. In actuality, the sample is skewed against drivers because passenger mutation markers appear in proportionally less instances than drivers do. To address the Class Imbalance Problem, improved K-Means + SMOTE are applied to the preprocessed data. The most crucial characteristics, including those at the gene and mutation levels, are then extracted from the balanced dataset. To lessen the computational load in terms of time, the best features from the retrieved features are selected using Forensic interpretation tailored hunger food search optimization (FIHFSO). The ideal features are used to train the deep learning classifier that conducts the separation procedure. In this research, an Improved Recurrent Neural Network (I-RNN) is used to make a final decision about genes. At 90% of learning percentage, the accuracy of the proposed method achieves 0.98% of 0.83, 0.81, 0.65, 0.80, 0.92 and 0.63% which is compared to the other methods like HGS, FBIO, AOA, AO, GOA and PRO respectively.

3.
BMC Bioinformatics ; 24(1): 376, 2023 Oct 04.
Artigo em Inglês | MEDLINE | ID: mdl-37794362

RESUMO

BACKGROUND: Protein methylation, a post-translational modification, is crucial in regulating various cellular functions. Arginine methylation is required to understand crucial biochemical activities and biological functions, like gene regulation, signal transduction, etc. However, some experimental methods, including Chip-Chip, mass spectrometry, and methylation-specific antibodies, exist for the prediction of methylated proteins. These experimental methods are expensive and tedious. As a result, computational methods based on machine learning play an efficient role in predicting arginine methylation sites. RESULTS: In this research, a novel method called PRMxAI has been proposed to predict arginine methylation sites. The proposed PRMxAI extract sequence-based features, such as dipeptide composition, physicochemical properties, amino acid composition, and information theory-based features (Arimoto, Havrda-Charvat, Renyi, and Shannon entropy), to represent the protein sequences into numerical format. Various machine learning algorithms are implemented to select the better classifier, such as Decision trees, Naive Bayes, Random Forest, Support vector machines, and K-nearest neighbors. The random forest algorithm is selected as the underlying classifier for the PRMxAI model. The performance of PRMxAI is evaluated by employing 10-fold cross-validation, and it yields 87.17% and 90.40% accuracy on mono-methylarginine and di-methylarginine data sets, respectively. This research also examines the impact of various features on both data sets using explainable artificial intelligence. CONCLUSIONS: The proposed PRMxAI shows the effectiveness of the features for predicting arginine methylation sites. Additionally, the SHapley Additive exPlanation method is used to interpret the predictive mechanism of the proposed model. The results indicate that the proposed PRMxAI model outperforms other state-of-the-art predictors.


Assuntos
Aminoácidos , Arginina , Aminoácidos/metabolismo , Arginina/química , Arginina/metabolismo , Metilação , Inteligência Artificial , Teorema de Bayes , Processamento de Proteína Pós-Traducional , Algoritmos
4.
Front Genet ; 14: 1154120, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37152988

RESUMO

Introduction: Essential genes are essential for the survival of various species. These genes are a family linked to critical cellular activities for species survival. These genes are coded for proteins that regulate central metabolism, gene translation, deoxyribonucleic acid replication, and fundamental cellular structure and facilitate intracellular and extracellular transport. Essential genes preserve crucial genomics information that may hold the key to a detailed knowledge of life and evolution. Essential gene studies have long been regarded as a vital topic in computational biology due to their relevance. An essential gene is composed of adenine, guanine, cytosine, and thymine and its various combinations. Methods: This paper presents a novel method of extracting information on the stationary patterns of nucleotides such as adenine, guanine, cytosine, and thymine in each gene. For this purpose, some co-occurrence matrices are derived that provide the statistical distribution of stationary patterns of nucleotides in the genes, which is helpful in establishing the relationship between the nucleotides. For extracting discriminant features from each co-occurrence matrix, energy, entropy, homogeneity, contrast, and dissimilarity features are computed, which are extracted from all co-occurrence matrices and then concatenated to form a feature vector representing each essential gene. Finally, supervised machine learning algorithms are applied for essential gene classification based on the extracted fixed-dimensional feature vectors. Results: For comparison, some existing state-of-the-art feature representation techniques such as Shannon entropy (SE), Hurst exponent (HE), fractal dimension (FD), and their combinations have been utilized. Discussion: An extensive experiment has been performed for classifying the essential genes of five species that show the robustness and effectiveness of the proposed methodology.

5.
Cluster Comput ; 26(1): 119-135, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-35125934

RESUMO

A sentiment analysis system has been proposed in this paper for pain detection using cutting edge techniques in a smart healthcare framework. This proposed system may be eligible for detecting pain sentiments by analyzing facial expressions on the human face. The implementation of the proposed system has been divided into four components. The first component is about detecting the face region from the input image using a tree-structured part model. Statistical and deep learning-based feature analysis has been performed in the second component to extract more valuable and distinctive patterns from the extracted facial region. In the third component, the prediction models based on statistical and deep feature analysis derive scores for the pain intensities (no-pain, low-pain, and high-pain) on the facial region. The scores due to the statistical and deep feature analysis are fused to enhance the performance of the proposed method in the fourth component. We have employed two benchmark facial pain expression databases during experimentation, such as UNBC-McMaster shoulder pain and 2D Face-set database with Pain-expression. The performance concerning these databases has been compared with some existing state-of-the-art methods. These comparisons show the superiority of the proposed system.

6.
Comput Biol Med ; 141: 105024, 2022 02.
Artigo em Inglês | MEDLINE | ID: mdl-34815067

RESUMO

BACKGROUND AND OBJECTIVE: The world is currently facing a global emergency due to COVID-19, which requires immediate strategies to strengthen healthcare facilities and prevent further deaths. To achieve effective remedies and solutions, research on different aspects, including the genomic and proteomic level characterizations of SARS-CoV-2, are critical. In this work, the spatial representation/composition and distribution frequency of 20 amino acids across the primary protein sequences of SARS-CoV-2 were examined according to different parameters. METHOD: To identify the spatial distribution of amino acids over the primary protein sequences of SARS-CoV-2, the Hurst exponent and Shannon entropy were applied as parameters to fetch the autocorrelation and amount of information over the spatial representations. The frequency distribution of each amino acid over the protein sequences was also evaluated. In the case of a one-dimensional sequence, the Hurst exponent (HE) was utilized due to its linear relationship with the fractal dimension (D), i.e. D+HE=2, to characterize fractality. Moreover, binary Shannon entropy was considered to measure the uncertainty in a binary sequence then further applied to calculate amino acid conservation in the primary protein sequences. RESULTS AND CONCLUSION: Fourteen (14) SARS-CoV protein sequences were evaluated and compared with 105 SARS-CoV-2 proteins. The simulation results demonstrate the differences in the collected information about the amino acid spatial distribution in the SARS-CoV-2 and SARS-CoV proteins, enabling researchers to distinguish between the two types of CoV. The spatial arrangement of amino acids also reveals similarities and dissimilarities among the important structural proteins, E, M, N and S, which is pivotal to establish an evolutionary tree with other CoV strains.


Assuntos
COVID-19 , SARS-CoV-2 , Sequência de Aminoácidos , Aminoácidos , Humanos , Proteômica
7.
Neural Netw ; 122: 407-419, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31794950

RESUMO

A novel method for person identification based on the fusion of iris and periocular biometrics has been proposed in this paper. The challenges for image acquisition for Near-Infrared or Visual Wavelength lights under constrained and unconstrained environments have been considered here. The proposed system is divided into image preprocessing data augmentation followed by feature learning for classification components. In image preprocessing an annular iris, the portion is segmented out from an eyeball image and then transformed into a fixed-sized image region. The parameters of iris localization have been used to extract the local periocular region. Due to different imaging environments, the images suffer from various noise artifacts which create data insufficiency and complicate the recognition task. To overcome this situation, a novel method for data augmentation technique has been introduced here. For features extraction and classification tasks well-known, VGG16, ResNet50, and Inception-v3 CNN architectures have been employed. The performance due to iris and periocular are fused together to increase the performance of the recognition system. The extensive experimental results have been demonstrated in four benchmark iris databases namely: MMU1, UPOL, CASIA-Iris-distance, and UBIRIS.v2. The comparison with the state-of-the-art methods with respect to these databases shows the robustness and effectiveness of the proposed approach.


Assuntos
Identificação Biométrica/métodos , Aprendizado Profundo , Processamento de Imagem Assistida por Computador/métodos , Iris , Algoritmos , Bases de Dados Factuais , Face , Humanos
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