Mckennawilliford6744

Given the patient to doctor ratio of 50,0001 in low income and middle-income countries, there is a need for automated heart sound classification system that can screen the Phonocardiogram (PCG) records in real-time. This paper proposes deep neural network architectures such as a one-dimensional convolutional neural network (1D-CNN) and Feed-forward Neural Network (F-NN) for the classification of unsegmented phonocardiogram (PCG) signal. The research paper aims to automate the feature engineering and feature selection process used in the analysis of the PCG signal. The original PCG signal is down-sampled at 500 Hz. Then they are divided into smaller time segments of 6 s epochs. Savitzky-Golay filter is used to suppress the high-frequency noises in the signal by data point smoothening. The processed data was then provided as an input to the proposed deep neural network (DNN) architectures. 1081 PCG records were used for training and validating the proposed DNN models. The Feed-forward Neural Network model with five hidden layers provided a better overall accuracy of 0.8565 with a sensitivity of 0.8673, and specificity of 0.8475. The balanced accuracy of the model was found to be 0.8574. The performance of the model was also studied using the Receiver Operating Characteristic (ROC) plot, which produced an Area Under the Curve (AUC) value of 0.857. The classification accuracy of the proposed models was compared to the related works on PCG signal analysis for cardiovascular disease detection. The DNN models studied in this study provided comparable performance in heart sound classification without the requirement of feature engineering and segmentation of heart sound signals.While proton therapy can offer increased sparing of healthy tissue compared with X-ray therapy, it can be difficult to predict whether a benefit can be expected for an individual patient. Predictive modelling may aid in this respect. However, the predictions of these models can be affected by uncertainties in radiobiological model parameters and in planned dose. The aim of this work is to present a Markov model that incorporates these uncertainties to compare clinical outcomes for individualised proton and X-ray therapy treatments. A time-inhomogeneous fuzzy Markov model was developed which estimates the response of a patient to a given treatment plan in terms of quality adjusted life years. These are calculated using the dose-dependent probabilities of tumour control and toxicities as transition probabilities in the model. Dose-volume data representing multiple isotropic patient set-up uncertainties and range uncertainties (for proton therapy) are included to model dose delivery uncertainties. The model was retrospectively applied to an example patient as a demonstration. When uncertainty in the radiobiological model parameter was considered, the model predicted that proton therapy would result in an improved clinical outcome compared with X-ray therapy. However, when dose delivery uncertainty was included, there was no difference between the two treatments. By incorporating uncertainties in the predictive modelling calculations, the fuzzy Markov concept was found to be well suited to providing a more holistic comparison of individualised treatment outcomes for proton and X-ray therapy. This may prove to be useful in model-based patient selection strategies.The evaporation and crystallization process for sessile saline droplets during depressurization is experimentally studied. The relationship between ambient pressure and the crystallization pattern is primarily discussed. When the ambient pressure is low, salt particles are easily formed at the droplet contact line. In contrast, when the ambient pressure is similar to atmospheric pressure, it is more likely for cubic crystals to be formed inside the droplet. By analysing the contact angle fluctuation during crystallization, the experimental results show that the growth of a cubic salt crystal under high ambient pressure or low salt concentration leads to a greater deformation of the liquid-gas interface and a larger contact angle fluctuation. Finally, the Peclet number Pe is introduced to reflect the ratio of the rate of ion advection to the rate of diffusion. The Pe number is larger at lower ambient pressure, which means that the external mass transfer and convection effect is more significant under low pressure, with salt particles easily formed at the droplet contact line. The effect of concentration diffusion inside the droplet increases at higher ambient pressure, thereby, making it easy for cubic crystals to be formed inside the droplet.The development of neuroimaging instrumentation has boosted neuroscience researches. Consequently, both the fineness and the cost of data acquisition have profoundly increased, leading to the main bottleneck of this field limited sample size and high dimensionality of neuroimaging data. Therefore, the emphasis of ideas of data pooling and research collaboration has increased over the past decade. Collaborative analysis techniques emerge as the idea developed. In this paper, we present NEURO-LEARN, a solution for collaborative pattern analysis of neuroimaging data. Its collaboration scheme consists of four parts projects, data, analysis, and reports. While data preparation workflows defined in projects reduce the high dimensionality of neuroimaging data by collaborative computation, pooling of derived data and sharing of pattern analysis workflows along with generated reports on the Web enlarge the sample size and ensure the reliability and reproducibility of pattern analysis. Incorporating this scheme, NEURO-LEARN provides an easy-to-use Web application that allows users from different sites to share projects and processed data, perform pattern analysis, and obtain result reports. We anticipate that this solution will help neuroscientists to enlarge sample size, conquer the curse of dimensionality and conduct reproducible studies on neuroimaging data with efficiency and validity.Diffusion MRI is the modality of choice to study alterations of white matter. In past years, various works have used diffusion MRI for automatic classification of Alzheimer's disease. However, classification performance obtained with different approaches is difficult to compare because of variations in components such as input data, participant selection, image preprocessing, feature extraction, feature rescaling (FR), feature selection (FS) and cross-validation (CV) procedures. Moreover, these studies are also difficult to reproduce because these different components are not readily available. In a previous work (Samper-González et al. 2018), we propose an open-source framework for the reproducible evaluation of AD classification from T1-weighted (T1w) MRI and PET data. click here In the present paper, we first extend this framework to diffusion MRI data. Specifically, we add conversion of diffusion MRI ADNI data into the BIDS standard and pipelines for diffusion MRI preprocessing and feature extraction. We then apply the framework to compare different components.