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PeerJ Comput Sci ; 7: e770, 2021.
Article in English | MEDLINE | ID: covidwho-1515635

ABSTRACT

The COVID-19 pandemic is the most serious catastrophe since the Second World War. To predict the epidemic more accurately under the influence of policies, a framework based on Independently Recurrent Neural Network (IndRNN) with fine-tuning are proposed for predict the epidemic development trend of confirmed cases and deaths in the United Stated, India, Brazil, France, Russia, China, and the world to late May, 2021. The proposed framework consists of four main steps: data pre-processing, model pre-training and weight saving, the weight fine-tuning, trend predicting and validating. It is concluded that the proposed framework based on IndRNN and fine-tuning with high speed and low complexity, has great fitting and prediction performance. The applied fine-tuning strategy can effectively reduce the error by up to 20.94% and time cost. For most of the countries, the MAPEs of fine-tuned IndRNN model were less than 1.2%, the minimum MAPE and RMSE were 0.05%, and 1.17, respectively, by using Chinese deaths, during the testing phase. According to the prediction and validation results, the MAPEs of the proposed framework were less than 6.2% in most cases, and it generated lowest MAPE and RMSE values of 0.05% and 2.14, respectively, for deaths in China. Moreover, Policies that play an important role in the development of COVID-19 have been summarized. Timely and appropriate measures can greatly reduce the spread of COVID-19; untimely and inappropriate government policies, lax regulations, and insufficient public cooperation are the reasons for the aggravation of the epidemic situations. The code is available at https://github.com/zhhongsh/COVID19-Precdiction. And the prediction by IndRNN model with fine-tuning are now available online (http://47.117.160.245:8088/IndRNNPredict).

2.
BMC Infect Dis ; 20(1): 818, 2020 Nov 10.
Article in English | MEDLINE | ID: covidwho-917921

ABSTRACT

BACKGROUND: To explore the kinetic changes in virology, specific antibody response and imaging during the clinical course of COVID-19. METHODS: This observational study enrolled 20 patients with COVID-19, who were hospitalized between January 20-April 6, 2020, in the two COVID-19 designated hospitals of Zhoushan, Zhejiang and Rushan, Shandong, China, The laboratory findings, imaging, serum response to viral infection, and viral RNA level in the throat and stool samples were assessed from onset to recovery phase in patients with COVID-19. RESULTS: SARS-COV-2 RNA was positive as early as day four. It remained positive until day 55 post-onset in the sputum-throat swabs and became negative in most cases (55%) within 14 days after onset. Lymphocytopenia occurred in 40% (8/20) of patients during the peak infection period and returned to normal at week five. The most severe inflammation in the lungs appeared in week 2 or 3 after onset, and this was completely absorbed between week 6 and 8 in 85.7% of patients. All patients had detectable antibodies to the receptor binding domain (RBD), and 95% of these patients had IgG to viral N proteins. The antibody titer peaked at week four. Anti-S IgM was positive in 7 of 20 patients after week three. CONCLUSIONS: All COVID-19 patients in this study were self-limiting and recovered well though it may take as long as 6-8 weeks. Our findings on the kinetic changes in imaging, serum response to viral infection and viral RNA level may help understand pathogenesis and define clinical course of COVID-19.


Subject(s)
Antibodies, Viral/blood , Betacoronavirus/immunology , Clinical Laboratory Techniques , Coronavirus Infections/diagnostic imaging , Coronavirus Infections/immunology , Lung/diagnostic imaging , Pneumonia, Viral/diagnostic imaging , Pneumonia, Viral/immunology , Adolescent , Adult , Aged , Betacoronavirus/genetics , COVID-19 , COVID-19 Testing , COVID-19 Vaccines , Child , China/epidemiology , Coronavirus Infections/diagnosis , Coronavirus Infections/epidemiology , Coronavirus Infections/virology , Coronavirus Nucleocapsid Proteins , Female , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Male , Middle Aged , Nucleocapsid Proteins/immunology , Pandemics , Phosphoproteins , Pneumonia, Viral/epidemiology , Pneumonia, Viral/virology , RNA, Viral/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , SARS-CoV-2 , Sputum/virology , Tomography, X-Ray Computed , Young Adult
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