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Genomics Proteomics & BioinformaticsGenomicsPeer-reviewed journal article

The global landscape of SARS-CoV-2 genomes, variants, and haplotypes in 2019nCoVR

Shuhui SongiD, Lina MaiD, Dong ZouiD, Dongmei TianiD, Cuiping LiiD, Junwei ZhuiD, Meili CheniD, Anke WangiD, Yingke MaiD, Mengwei LiiD, Xufei TengiD, Ying CuiiD, Guangya DuaniD, Mochen ZhangiD, Tong JiniD, Cheng‐Min ShiiD, Zhenglin DuiD, Yadong ZhangiD, Chuandong LiuiD, Rujiao LiiD, Jingyao ZengiD, Lili HaoiD, Shuai JiangiD, Hua CheniD, Dali HaniD, , Yīmíng BàoiD

PDFDOIPreprint

Abstract

On 22 January 2020, the National Genomics Data Center (NGDC), part of the China National Center for Bioinformation (CNCB), created the 2019 Novel Coronavirus Resource (2019nCoVR), an open-access SARS-CoV-2 information resource. 2019nCoVR features a comprehensive integration of sequence and clinical information for all publicly available SARS-CoV-2 isolates, which are manually curated with value-added annotations and quality evaluated by our in-house automated pipeline. Of particular note, 2019nCoVR performs systematic analyses to generate a dynamic landscape of SARS-CoV-2 genomic variations at a global scale. It provides all identified variants and detailed statistics for each virus isolate, and congregates the quality score, functional annotation, and population frequency for each variant. It also generates visualization of the spatiotemporal change for each variant and yields historical viral haplotype network maps for the course of the outbreak from all complete and high-quality genomes. Moreover, 2019nCoVR provides a full collection of SARS-CoV-2 relevant literature on COVID-19 (Coronavirus Disease 2019), including published papers from PubMed as well as preprints from services such as bioRxiv and medRxiv through Europe PMC. Furthermore, by linking with relevant databases in CNCB-NGDC, 2019nCoVR offers data submission services for raw sequence reads and assembled genomes, and data sharing with National Center for Biotechnology Information. Collectively, all SARS-CoV-2 genome sequences, variants, haplotypes and literature are updated daily to provide timely information, making 2019nCoVR a valuable resource for the global research community. 2019nCoVR is accessible at https://bigd.big.ac.cn/ncov/.

Citations
112
FWCI
3.14
Field percentile
top 5%

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