High-coverage SARS-CoV-2 genome sequences acquired by target capture sequencing.
Shao-Qing WenChang SunHuanying ZhengLingxiang WangHuan ZhangLirong ZouZhe LiuPanxin DuXuding XuLijun LiangXiaofang PengWei ZhangJie WuJiyuan YangBo LeiGuangyi ZengChangwen KeFang ChenXiao ZhangPublished in: Journal of medical virology (2020)
In this study, we designed a set of SARS-CoV-2 enrichment probes to increase the capacity for sequence-based virus detection and obtain the comprehensive genome sequence at the same time. This universal SARS-CoV-2 enrichment probe set contains 502 120 nt single-stranded DNA biotin-labeled probes designed based on all available SARS-CoV-2 viral sequences and it can be used to enrich for SARS-CoV-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 cell culture, three nasopharyngeal swab samples (cycle threshold [Ct ] values: 32.36, 36.72, and 38.44) from patients diagnosed with COVID-19 (positive control) and four throat swab samples from patients without COVID-19 (negative controls), respectively. Moreover, based on these high-quality sequences, we discuss the heterozygosity and viral expression during coronavirus replication and its phylogenetic relationship with other selected high-quality samples from the Genome Variation Map. Therefore, this universal SARS-CoV-2 enrichment probe system can capture and enrich SARS-CoV-2 viral sequences selectively and effectively in different samples, especially clinical swab samples with a relatively low concentration of viral particles.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- end stage renal disease
- ejection fraction
- healthcare
- newly diagnosed
- chronic kidney disease
- living cells
- computed tomography
- small molecule
- prognostic factors
- public health
- single molecule
- peritoneal dialysis
- coronavirus disease
- poor prognosis
- dna methylation
- gene expression
- cell proliferation
- binding protein
- genome wide
- magnetic resonance imaging
- nucleic acid
- single cell
- pet imaging
- amino acid
- patient reported
- cell cycle
- contrast enhanced