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本文引用的文献

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Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection.14株严重急性呼吸综合征冠状病毒分离株的全长基因组序列比较分析及与假定感染源相关的常见突变
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Aetiology: Koch's postulates fulfilled for SARS virus.病因:SARS病毒符合科赫法则。
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The Genome sequence of the SARS-associated coronavirus.与严重急性呼吸综合征相关的冠状病毒的基因组序列。
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Identification of a novel coronavirus in patients with severe acute respiratory syndrome.在严重急性呼吸综合征患者中鉴定出一种新型冠状病毒。
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Gene expression analysis using oligonucleotide arrays produced by maskless photolithography.使用无掩膜光刻法制备的寡核苷酸阵列进行基因表达分析。
Genome Res. 2002 Nov;12(11):1749-55. doi: 10.1101/gr.362402.
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Sequencing by hybridization (SBH): advantages, achievements, and opportunities.杂交测序(SBH):优势、成果与机遇。
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Assessing DNA sequence variations in human ESTs in a phylogenetic context using high-density oligonucleotide arrays.在系统发育背景下使用高密度寡核苷酸阵列评估人类EST中的DNA序列变异。
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High-throughput variation detection and genotyping using microarrays.使用微阵列进行高通量变异检测和基因分型。
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Sequencing by hybridization arrays.杂交阵列测序
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Minimising the secondary structure of DNA targets by incorporation of a modified deoxynucleoside: implications for nucleic acid analysis by hybridisation.通过掺入修饰的脱氧核苷使DNA靶标的二级结构最小化:对杂交核酸分析的影响。
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利用高通量、高密度重测序阵列追踪严重急性呼吸综合征冠状病毒的进化

Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arrays.

作者信息

Wong Christopher W, Albert Thomas J, Vega Vinsensius B, Norton Jason E, Cutler David J, Richmond Todd A, Stanton Lawrence W, Liu Edison T, Miller Lance D

机构信息

Genome Institute of Singapore, Singapore 138672, Republic of Singapore.

出版信息

Genome Res. 2004 Mar;14(3):398-405. doi: 10.1101/gr.2141004.

DOI:10.1101/gr.2141004
PMID:14993206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC353227/
Abstract

Mutations in the SARS-Coronavirus (SARS-CoV) can alter its clinical presentation, and the study of its mutation patterns in human populations can facilitate contact tracing. Here, we describe the development and validation of an oligonucleotide resequencing array for interrogating the entire 30-kb SARS-CoV genome in a rapid, cost-effective fashion. Using this platform, we sequenced SARS-CoV genomes from Vero cell culture isolates of 12 patients and directly from four patient tissues. The sequence obtained from the array is highly reproducible, accurate (>99.99% accuracy) and capable of identifying known and novel variants of SARS-CoV. Notably, we applied this technology to a field specimen of probable SARS and rapidly deduced its infectious source. We demonstrate that array-based resequencing-by-hybridization is a fast, reliable, and economical alternative to capillary sequencing for obtaining SARS-CoV genomic sequence on a population scale, making this an ideal platform for the global monitoring of SARS-CoV and other small-genome pathogens.

摘要

严重急性呼吸综合征冠状病毒(SARS-CoV)的突变可改变其临床表现,而对其在人群中的突变模式进行研究有助于接触者追踪。在此,我们描述了一种寡核苷酸重测序阵列的开发与验证,该阵列能够以快速且经济高效的方式对整个30 kb的SARS-CoV基因组进行检测。利用这个平台,我们对12例患者的Vero细胞培养分离株以及直接从4例患者组织中提取的SARS-CoV基因组进行了测序。从阵列获得的序列具有高度可重复性、准确性高(准确率>99.99%),并且能够识别SARS-CoV的已知和新型变体。值得注意的是,我们将这项技术应用于一份可能感染SARS的现场样本,并迅速推断出其传染源。我们证明,基于阵列的杂交重测序是一种在群体规模上获取SARS-CoV基因组序列的快速、可靠且经济的替代毛细管测序的方法,使其成为全球监测SARS-CoV和其他小基因组病原体的理想平台。