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Register a new userOnline unsupervised Learning for domain shift in COVID-19 CT scan datasets
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Neural networks often require large amounts of expert annotated data to train. When changes are made in the process of medical imaging, trained networks may not perform as well, and obtaining large amounts of expert annotations for each change in the imaging process can be time consuming and expensive. Online unsupervised learning is a method that has been proposed to deal with situations where there is a domain shift in incoming data, and a lack of annotations. The aim of this study is to see whether online unsupervised learning can help COVID-19 CT scan classification models adjust to slight domain shifts, when there are no annotations available for the new data. A total of six experiments are performed using three test datasets with differing amounts of domain shift. These experiments compare the performance of the online unsupervised learning strategy to a baseline, as well as comparing how the strategy performs on different domain shifts. Code for online unsupervised learning can be found at this link: https://github.com/Mewtwo/online-unsupervised-learning
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In this worldwide spread of SARS-CoV-2 (COVID-19) infection, it is of utmost importance to detect the disease at an early stage especially in the hot spots of this epidemic. There are more than 110 Million infected cases on the globe, sofar. Due to its promptness and effective results computed tomography (CT)-scan image is preferred to the reverse-transcription polymerase chain reaction (RT-PCR). Early detection and isolation of the patient is the only possible way of controlling the spread of the disease. Automated analysis of CT-Scans can provide enormous support in this process. In this article, We propose a novel approach to detect SARS-CoV-2 using CT-scan images. Our method is based on a very intuitive and natural idea of analyzing shapes, an attempt to mimic a professional medic. We mainly trace SARS-CoV-2 features by quantifying their topological properties. We primarily use a tool called persistent homology, from Topological Data Analysis (TDA), to compute these topological properties. We train and test our model on the SARS-CoV-2 CT-scan dataset citep{soares2020sars}, an open-source dataset, containing 2,481 CT-scans of normal and COVID-19 patients. Our model yielded an overall benchmark F1 score of $99.42% $, accuracy $99.416%$, precision $99.41%$, and recall $99.42%$. The TDA techniques have great potential that can be utilized for efficient and prompt detection of COVID-19. The immense potential of TDA may be exploited in clinics for rapid and safe detection of COVID-19 globally, in particular in the low and middle-income countries where RT-PCR labs and/or kits are in a serious crisis.
The coronavirus disease, named COVID-19, has become the largest global public health crisis since it started in early 2020. CT imaging has been used as a complementary tool to assist early screening, especially for the rapid identification of COVID-19 cases from community acquired pneumonia (CAP) cases. The main challenge in early screening is how to model the confusing cases in the COVID-19 and CAP groups, with very similar clinical manifestations and imaging features. To tackle this challenge, we propose an Uncertainty Vertex-weighted Hypergraph Learning (UVHL) method to identify COVID-19 from CAP using CT images. In particular, multiple types of features (including regional features and radiomics features) are first extracted from CT image for each case. Then, the relationship among different cases is formulated by a hypergraph structure, with each case represented as a vertex in the hypergraph. The uncertainty of each vertex is further computed with an uncertainty score measurement and used as a weight in the hypergraph. Finally, a learning process of the vertex-weighted hypergraph is used to predict whether a new testing case belongs to COVID-19 or not. Experiments on a large multi-center pneumonia dataset, consisting of 2,148 COVID-19 cases and 1,182 CAP cases from five hospitals, are conducted to evaluate the performance of the proposed method. Results demonstrate the effectiveness and robustness of our proposed method on the identification of COVID-19 in comparison to state-of-the-art methods.
The capability of generalization to unseen domains is crucial for deep learning models when considering real-world scenarios. However, current available medical image datasets, such as those for COVID-19 CT images, have large variations of infections and domain shift problems. To address this issue, we propose a prior knowledge driven domain adaptation and a dual-domain enhanced self-correction learning scheme. Based on the novel learning schemes, a domain adaptation based self-correction model (DASC-Net) is proposed for COVID-19 infection segmentation on CT images. DASC-Net consists of a novel attention and feature domain enhanced domain adaptation model (AFD-DA) to solve the domain shifts and a self-correction learning process to refine segmentation results. The innovations in AFD-DA include an image-level activation feature extractor with attention to lung abnormalities and a multi-level discrimination module for hierarchical feature domain alignment. The proposed self-correction learning process adaptively aggregates the learned model and corresponding pseudo labels for the propagation of aligned source and target domain information to alleviate the overfitting to noises caused by pseudo labels. Extensive experiments over three publicly available COVID-19 CT datasets demonstrate that DASC-Net consistently outperforms state-of-the-art segmentation, domain shift, and coronavirus infection segmentation methods. Ablation analysis further shows the effectiveness of the major components in our model. The DASC-Net enriches the theory of domain adaptation and self-correction learning in medical imaging and can be generalized to multi-site COVID-19 infection segmentation on CT images for clinical deployment.
With the rapidly worldwide spread of Coronavirus disease (COVID-19), it is of great importance to conduct early diagnosis of COVID-19 and predict the time that patients might convert to the severe stage, for designing effective treatment plan and reducing the clinicians workloads. In this study, we propose a joint classification and regression method to determine whether the patient would develop severe symptoms in the later time, and if yes, predict the possible conversion time that the patient would spend to convert to the severe stage. To do this, the proposed method takes into account 1) the weight for each sample to reduce the outliers influence and explore the problem of imbalance classification, and 2) the weight for each feature via a sparsity regularization term to remove the redundant features of high-dimensional data and learn the shared information across the classification task and the regression task. To our knowledge, this study is the first work to predict the disease progression and the conversion time, which could help clinicians to deal with the potential severe cases in time or even save the patients lives. Experimental analysis was conducted on a real data set from two hospitals with 422 chest computed tomography (CT) scans, where 52 cases were converted to severe on average 5.64 days and 34 cases were severe at admission. Results show that our method achieves the best classification (e.g., 85.91% of accuracy) and regression (e.g., 0.462 of the correlation coefficient) performance, compared to all comparison methods. Moreover, our proposed method yields 76.97% of accuracy for predicting the severe cases, 0.524 of the correlation coefficient, and 0.55 days difference for the converted time.
We present an automatic COVID1-19 diagnosis framework from lung CT images. The focus is on signal processing and classification on small datasets with efforts putting into exploring data preparation and augmentation to improve the generalization capability of the 2D CNN classification models. We propose a unique and effective data augmentation method using multiple Hounsfield Unit (HU) normalization windows. In addition, the original slice image is cropped to exclude background, and a filter is applied to filter out closed-lung images. For the classification network, we choose to use 2D Densenet and Xception with the feature pyramid network (FPN). To further improve the classification accuracy, an ensemble of multiple CNN models and HU windows is used. On the training/validation dataset, we achieve a patient classification accuracy of 93.39%.
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