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Updated: Jul 21, 2025

Visualization of SARS-CoV-2 using Immuno RNA-Fluorescence In Situ Hybridization
Published on: December 23, 2020
COVIDanno, COVID-19 annotation in human
Yuzhou Feng1,2, Mengyuan Yang3, Zhiwei Fan4,5
1West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Abstract:
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiologic agent of coronavirus disease 19 (COVID-19), has caused a global health crisis. Despite ongoing efforts to treat patients, there is no universal prevention or cure available. One of the feasible approaches will be identifying the key genes from SARS-CoV-2-infected cells. SARS-CoV-2-infected in vitro model, allows easy control of the experimental conditions, obtaining reproducible results, and monitoring of infection progression. Currently, accumulating RNA-seq data from SARS-CoV-2 in vitro models urgently needs systematic translation and interpretation. To fill this gap, we built COVIDanno, COVID-19 annotation in humans, available at http://biomedbdc.wchscu.cn/COVIDanno/. The aim of this resource is to provide a reference resource of intensive functional annotations of differentially expressed genes (DEGs) among different time points of COVID-19 infection in human in vitro models. To do this, we performed differential expression analysis for 136 individual datasets across 13 tissue types. In total, we identified 4,935 DEGs. We performed multiple bioinformatics/computational biology studies for these DEGs. Furthermore, we developed a novel tool to help users predict the status of SARS-CoV-2 infection for a given sample. COVIDanno will be a valuable resource for identifying SARS-CoV-2-related genes and understanding their potential functional roles in different time points and multiple tissue types.
Insights
Researchers identified key genes involved in COVID-19 infection using SARS-CoV-2 models. This study provides a valuable resource for understanding the functional roles of these differentially expressed genes.
Area of Science:
- Genomics
- Bioinformatics
- Infectious Diseases
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19, a global health crisis with no universal cure.
- Identifying key genes in infected cells is crucial for understanding and potentially treating the disease.
- Existing RNA-seq data from SARS-CoV-2 in vitro models requires systematic interpretation.
Purpose of the Study:
- To create a comprehensive annotation resource for differentially expressed genes (DEGs) in human in vitro models of COVID-19.
- To facilitate the identification and functional analysis of SARS-CoV-2-related genes.
- To develop a tool for predicting SARS-CoV-2 infection status.
Main Methods:
- Performed differential expression analysis on 136 RNA-seq datasets from SARS-CoV-2 infected human in vitro models across 13 tissue types.
- Conducted extensive bioinformatics and computational biology analyses on identified DEGs.
- Developed a novel prediction tool for SARS-CoV-2 infection status.
Main Results:
- Identified a total of 4,935 differentially expressed genes (DEGs) across various time points and tissue types.
- Generated intensive functional annotations for these DEGs.
- Developed a functional tool to predict SARS-CoV-2 infection status.
Conclusions:
- COVIDanno serves as a valuable reference resource for COVID-19 research.
- The identified DEGs and their annotations aid in understanding gene functions during SARS-CoV-2 infection.
- The developed tool assists in sample infection status prediction, advancing COVID-19 diagnostics and research.
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