Author: Wen, Shaoqing; Sun, Chang; Zheng, Huanying; Wang, Lingxiang; Zhang, Huan; Zou, Lirong; Liu, Zhe; Du, Panxin; Xu, Xuding; Liang, Lijun; Peng, Xiaofang; Zhang, Wei; Wu, Jie; Yang, Jiyuan; Lei, Bo; Zeng, Guangyi; Ke, Changwen; Chen, Fang; Zhang, Xiao
Title: Highâ€Coverage SARSâ€CoVâ€2 Genome Sequences Acquired by Target Capture Sequencing Cord-id: dfjzse77 Document date: 2020_6_3
ID: dfjzse77
Snippet: In this study, we designed a set of SARSâ€CoVâ€2 enrichment probes to increase the capacity for sequenceâ€based virus detection and obtain the comprehensive genome sequence at the same time. This universal SARSâ€CoVâ€2 enrichment probe set contains 502 120nt ssDNA biotinâ€labeled probes designed based on all available SARSâ€CoVâ€2 viral sequences and it can be used to enrich for SARSâ€CoVâ€2 sequences without prior knowledge of type or subtype. Following the CDC health and safety guide
Document: In this study, we designed a set of SARSâ€CoVâ€2 enrichment probes to increase the capacity for sequenceâ€based virus detection and obtain the comprehensive genome sequence at the same time. This universal SARSâ€CoVâ€2 enrichment probe set contains 502 120nt ssDNA biotinâ€labeled probes designed based on all available SARSâ€CoVâ€2 viral sequences and it can be used to enrich for SARSâ€CoVâ€2 sequences without prior knowledge of type or subtype. Following the CDC health and safety guidelines, marked enrichment was demonstrated in a virus strain sample from a cell culture, three nasopharyngeal swab samples (cycle threshold [Ct] values: 32.36, 36.72, and 38.44) from patients diagnosed with COVIDâ€19 (positive control) and four throat swab samples from patients without COVIDâ€19 (negative controls), respectively. Moreover, based on these highâ€quality sequences, we discuss the heterozygosity and viral expression during coronavirus replication, and its phylogenetic relationship with other selected highâ€quality samples from The Genome Variation Map (GVM). Therefore, this universal SARSâ€CoVâ€2 enrichment probe system can capture and enrich SARSâ€CoVâ€2 viral sequences selectively and effectively in different samples, especially clinical swab samples with a relatively low concentration of viral particles. This article is protected by copyright. All rights reserved.
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