Low-dose CT with a deep convolutional neural network blocks model using mean squared error loss and structural similar loss

Author(s):  
Yinjin Ma ◽  
Peng Feng ◽  
Peng He ◽  
Zourong Long ◽  
Biao Wei
2020 ◽  
Vol 39 (7) ◽  
pp. 2289-2301 ◽  
Author(s):  
Meng Li ◽  
William Hsu ◽  
Xiaodong Xie ◽  
Jason Cong ◽  
Wen Gao

2017 ◽  
Vol 36 (12) ◽  
pp. 2524-2535 ◽  
Author(s):  
Hu Chen ◽  
Yi Zhang ◽  
Mannudeep K. Kalra ◽  
Feng Lin ◽  
Yang Chen ◽  
...  

2021 ◽  
Author(s):  
Seyyedomid Badretale

An essential objective in low-dose Computed Tomography (CT) imaging is how best to preserve the image quality. While the image quality lowers with reducing the X-ray dosage, improving the quality is crucial. Therefore, a novel method to denoise low-dose CT images has been presented in this thesis. Different from the traditional algorithms which utilize similar shared features of CT images in the spatial domain, the deep learning approaches are suggested for low-dose CT denoising. The proposed algorithm learns an end-to-end mapping from the low-dose CT images for denoising the low-dose CT images. The first method is based on a fully convolutional neural network. The second approach is a deep convolutional neural network architecture consisting of five major sections. The results of two frameworks are compared with the state-of-the-art methods. Several metrics for assessing image quality are applied in this thesis in order to highlight the supremacy of the performed method.


Genes ◽  
2019 ◽  
Vol 10 (11) ◽  
pp. 862
Author(s):  
Tong Liu ◽  
Zheng Wang

We present a deep-learning package named HiCNN2 to learn the mapping between low-resolution and high-resolution Hi-C (a technique for capturing genome-wide chromatin interactions) data, which can enhance the resolution of Hi-C interaction matrices. The HiCNN2 package includes three methods each with a different deep learning architecture: HiCNN2-1 is based on one single convolutional neural network (ConvNet); HiCNN2-2 consists of an ensemble of two different ConvNets; and HiCNN2-3 is an ensemble of three different ConvNets. Our evaluation results indicate that HiCNN2-enhanced high-resolution Hi-C data achieve smaller mean squared error and higher Pearson’s correlation coefficients with experimental high-resolution Hi-C data compared with existing methods HiCPlus and HiCNN. Moreover, all of the three HiCNN2 methods can recover more significant interactions detected by Fit-Hi-C compared to HiCPlus and HiCNN. Based on our evaluation results, we would recommend using HiCNN2-1 and HiCNN2-3 if recovering more significant interactions from Hi-C data is of interest, and HiCNN2-2 and HiCNN if the goal is to achieve higher reproducibility scores between the enhanced Hi-C matrix and the real high-resolution Hi-C matrix.


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