
A review study: Computational techniques for expecting the impact of non-synonymous single nucleotide variants in human diseases
Non-Synonymous Single-Nucleotide Variants (nsSNVs) and mutations can create a diversity effect on proteins as changing genotype and phenotype, which interrupts its stability. The alterations in the protein stability may cause diseases like cancer. Discovering of nsSNVs and mutations can be a useful tool for diagnosing the disease at a beginning stage. Many studies introduced the various predicting singular and consensus tools that based on different Machine Learning Techniques (MLTs) using diverse datasets. Therefore, we introduce the current comprehensive review of the most popular and recent

Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics): Preface
[No abstract available]

Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics): Preface
[No abstract available]

Automated detection of shockable ECG signals: A review
Sudden cardiac death from lethal arrhythmia is a preventable cause of death. Ventricular fibrillation and tachycardia are shockable electrocardiographic (ECG)rhythms that can respond to emergency electrical shock therapy and revert to normal sinus rhythm if diagnosed early upon cardiac arrest with the restoration of adequate cardiac pump function. However, manual inspection of ECG signals is a difficult task in the acute setting. Thus, computer-aided arrhythmia classification (CAAC) systems have been developed to detect shockable ECG rhythm. Traditional machine learning and deep learning

Detection of myocardial infarction based on novel deep transfer learning methods for urban healthcare in smart cities
One of the common cardiac disorders is a cardiac attack called Myocardial infarction (MI), which occurs due to the blockage of one or more coronary arteries. Timely treatment of MI is important and slight delay results in severe consequences. Electrocardiogram (ECG) is the main diagnostic tool to monitor and reveal the MI signals. The complex nature of MI signals along with noise poses challenges to doctors for accurate and quick diagnosis. Manually studying large amounts of ECG data can be tedious and time-consuming. Therefore, there is a need for methods to automatically analyze the ECG data
Classification of Thyroid Carcinoma in Whole Slide Images Using Cascaded CNN
The objective of this research is to build a 'Whole Slide Images' classification system using Convolutional Neural Network (CNN). This system is capable of classifying Thyroid tumors into three types: Follicular adenoma, follicular carcinoma, and papillary carcinoma. Furthermore, the cascaded CNN technique is additionally employed to classify the classified follicular carcinoma into four subclasses: follicular carcinoma, papillary follicular variant, well-differentiated follicular carcinoma, and Poorly-differentiated follicular carcinoma. Results of the proposed CNN architecture showed
Convolutional neural networks for deep feature learning in retinal vessel segmentation
Analysis of retinal vessels in fundus images provides a valuable tool for characterizing many retinal and systemic diseases. Accurate automatic segmentation of these vessels is usually required as an essential analysis step. In this work, we propose a new formulation of deep Convolutional Neural Networks that allows simple and accurate segmentation of the retinal vessels. A major modification in this work is to reduce the intra-class variance by formulating the problem as a Three-class problem that differentiates: large vessels, small vessels, and background areas. In addition, different sizes

Computational identification of tissue-specific splicing regulatory elements in human genes from RNA-Seq Data
Alternative splicing is a vital process for regulating gene expression and promoting proteomic diversity. It plays a key role in tissue-specific expressed genes. This specificity is mainly regulated by splicing factors that bind to specific sequences called splicing regulatory elements (SREs). Here, we report a genome-wide analysis to study alternative splicing on multiple tissues, including brain, heart, liver, and muscle. We propose a pipeline to identify differential exons across tissues and hence tissue-specific SREs. In our pipeline, we utilize the DEXSeq package along with our previously

Segmentation of the right ventricle in MRI images using a dual active shape model
Active shape models (ASM) showed to have potential for segmenting the right ventricle (RV) in cardiac magnetic resonance images (MRIs). Nevertheless, the large variability and complexity of the RV shape do not allow for concisely capturing all possible shape variations among patients and anatomical cross-sections. Noticeably, the latter increases the number of iterations required to converge to a proper solution and reduces the segmentation accuracy. In this study, the authors propose a new ASM framework that can model the RV shape in short-axis cardiac MRI images. In this framework, the RV

Automatic localization of the left ventricle in cardiac MRI images using deep learning
Automatic localization of the left ventricle (LV) in cardiac MRI images is an essential step for automatic segmentation, functional analysis, and content based retrieval of cardiac images. In this paper, we introduce a new approach based on deep Convolutional Neural Network (CNN) to localize the LV in cardiac MRI in short axis views. A six-layer CNN with different kernel sizes was employed for feature extraction, followed by Softmax fully connected layer for classification. The pyramids of scales analysis was introduced in order to take account of the different sizes of the heart. A publically
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