• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Oxford Screening CSF and Respiratory samples ('OSCAR'): results of a pilot study to screen clinical samples from a diagnostic microbiology laboratory for viruses using Illumina next generation sequencing.牛津脑脊液和呼吸道样本筛查(“OSCAR”):一项试点研究的结果,该研究使用Illumina下一代测序技术对诊断微生物学实验室的临床样本进行病毒筛查。
BMC Res Notes. 2018 Feb 9;11(1):120. doi: 10.1186/s13104-018-3234-8.
2
A streamlined clinical metagenomic sequencing protocol for rapid pathogen identification.一种用于快速病原体鉴定的简化临床宏基因组测序方案。
Sci Rep. 2021 Feb 23;11(1):4405. doi: 10.1038/s41598-021-83812-x.
3
Development and Optimization of Metagenomic Next-Generation Sequencing Methods for Cerebrospinal Fluid Diagnostics.宏基因组下一代测序方法在脑脊液诊断中的开发和优化。
J Clin Microbiol. 2018 Aug 27;56(9). doi: 10.1128/JCM.00472-18. Print 2018 Sep.
4
Reduction of Human DNA Contamination in Clinical Cerebrospinal Fluid Specimens Improves the Sensitivity of Metagenomic Next-Generation Sequencing.降低临床脑脊液标本中人 DNA 污染可提高宏基因组下一代测序的灵敏度。
J Mol Neurosci. 2020 May;70(5):659-666. doi: 10.1007/s12031-019-01472-z. Epub 2020 Jan 31.
5
Clinical Metagenomic Sequencing for Diagnosis of Meningitis and Encephalitis.临床宏基因组测序在脑膜炎和脑炎诊断中的应用。
N Engl J Med. 2019 Jun 13;380(24):2327-2340. doi: 10.1056/NEJMoa1803396.
6
Clinical Metagenomic Next-Generation Sequencing for Pathogen Detection.临床宏基因组下一代测序在病原体检测中的应用。
Annu Rev Pathol. 2019 Jan 24;14:319-338. doi: 10.1146/annurev-pathmechdis-012418-012751. Epub 2018 Oct 24.
7
The Application of Metagenomic Next-Generation Sequencing in Detection of Pathogen in Bronchoalveolar Lavage Fluid and Sputum Samples of Patients with Pulmonary Infection.宏基因组下一代测序在检测肺部感染患者支气管肺泡灌洗液和痰液样本中的病原体中的应用。
Comput Math Methods Med. 2021 Nov 8;2021:7238495. doi: 10.1155/2021/7238495. eCollection 2021.
8
Evaluating metagenomics and targeted approaches for diagnosis and surveillance of viruses.评估宏基因组学和靶向方法在病毒诊断和监测中的应用。
Genome Med. 2024 Sep 9;16(1):111. doi: 10.1186/s13073-024-01380-x.
9
Real-time analysis of nanopore-based metagenomic sequencing from infected orthopaedic devices.基于纳米孔的宏基因组测序实时分析感染骨科设备。
BMC Genomics. 2018 Sep 27;19(1):714. doi: 10.1186/s12864-018-5094-y.
10
InteMAP: Integrated metagenomic assembly pipeline for NGS short reads.InteMAP:用于NGS短读长的综合宏基因组组装流程
BMC Bioinformatics. 2015 Aug 7;16:244. doi: 10.1186/s12859-015-0686-x.

引用本文的文献

1
Rhinovirus/enterovirus was the most common respiratory virus detected in adults with severe acute respiratory infections pre-COVID-19 in Kuala Lumpur, Malaysia.在马来西亚吉隆坡,呼吸道合胞病毒/肠病毒是 COVID-19 之前严重急性呼吸道感染的成年人中最常见的呼吸道病毒。
PLoS One. 2022 Sep 2;17(9):e0273697. doi: 10.1371/journal.pone.0273697. eCollection 2022.
2
Enhanced DNA and RNA pathogen detection via metagenomic sequencing in patients with pneumonia.通过宏基因组测序增强对肺炎患者DNA和RNA病原体的检测
J Transl Med. 2022 May 4;20(1):195. doi: 10.1186/s12967-022-03397-5.
3
Detection of respiratory viruses in adults with suspected COVID-19 in Kuala Lumpur, Malaysia.马来西亚吉隆坡疑似 COVID-19 成人呼吸道病毒检测。
J Clin Virol. 2021 Dec;145:105000. doi: 10.1016/j.jcv.2021.105000. Epub 2021 Oct 20.
4
Human Herpesvirus Sequencing in the Genomic Era: The Growing Ranks of the Herpetic Legion.基因组时代的人类疱疹病毒测序:疱疹军团不断壮大的队伍
Pathogens. 2019 Oct 12;8(4):186. doi: 10.3390/pathogens8040186.

本文引用的文献

1
HHV-6 reactivation as a cause of fever in autologous hematopoietic stem cell transplant recipients.HHV-6 再激活是自体造血干细胞移植受者发热的原因。
J Infect. 2017 Aug;75(2):155-159. doi: 10.1016/j.jinf.2017.05.011. Epub 2017 May 24.
2
Molecular Diagnosis of Orthopedic-Device-Related Infection Directly from Sonication Fluid by Metagenomic Sequencing.通过宏基因组测序直接从超声处理液中对骨科器械相关感染进行分子诊断。
J Clin Microbiol. 2017 Aug;55(8):2334-2347. doi: 10.1128/JCM.00462-17. Epub 2017 May 10.
3
metaSPAdes: a new versatile metagenomic assembler.metaSPAdes:一种新型通用宏基因组序列拼接软件
Genome Res. 2017 May;27(5):824-834. doi: 10.1101/gr.213959.116. Epub 2017 Mar 15.
4
Rapid Metagenomic Next-Generation Sequencing during an Investigation of Hospital-Acquired Human Parainfluenza Virus 3 Infections.医院获得性人副流感病毒3型感染调查期间的快速宏基因组下一代测序
J Clin Microbiol. 2016 Dec 28;55(1):177-182. doi: 10.1128/JCM.01881-16. Print 2017 Jan.
5
Fast and sensitive taxonomic classification for metagenomics with Kaiju.使用Kaiju对宏基因组学进行快速且灵敏的分类学分类。
Nat Commun. 2016 Apr 13;7:11257. doi: 10.1038/ncomms11257.
6
Unbiased Detection of Respiratory Viruses by Use of RNA Sequencing-Based Metagenomics: a Systematic Comparison to a Commercial PCR Panel.基于RNA测序的宏基因组学对呼吸道病毒的无偏检测:与商业PCR检测板的系统比较
J Clin Microbiol. 2016 Apr;54(4):1000-7. doi: 10.1128/JCM.03060-15. Epub 2016 Jan 27.
7
Development of a candidate reference material for adventitious virus detection in vaccine and biologicals manufacturing by deep sequencing.通过深度测序开发用于疫苗和生物制品生产中检测外源病毒的候选参考物质。
Vaccine. 2016 Apr 12;34(17):2035-43. doi: 10.1016/j.vaccine.2015.12.020. Epub 2015 Dec 19.
8
Next-generation sequencing (NGS) in the identification of encephalitis-causing viruses: Unexpected detection of human herpesvirus 1 while searching for RNA pathogens.下一代测序(NGS)在鉴定引起脑炎的病毒中的应用:在寻找RNA病原体时意外检测到人类疱疹病毒1型
J Virol Methods. 2015 Dec 15;226:1-6. doi: 10.1016/j.jviromet.2015.09.010. Epub 2015 Sep 28.
9
HHV-6 encephalitis may complicate the early phase after allogeneic hematopoietic stem cell transplantation: Detection by qualitative multiplex PCR and subsequent quantitative real-time PCR.HHV-6 脑炎可能在异基因造血干细胞移植后的早期阶段复杂化:通过定性多重 PCR 检测和随后的定量实时 PCR。
J Med Virol. 2016 Feb;88(2):319-23. doi: 10.1002/jmv.24340. Epub 2015 Aug 20.
10
Kraken: ultrafast metagenomic sequence classification using exact alignments.克拉肯:使用精确比对的超快速宏基因组序列分类
Genome Biol. 2014 Mar 3;15(3):R46. doi: 10.1186/gb-2014-15-3-r46.

牛津脑脊液和呼吸道样本筛查(“OSCAR”):一项试点研究的结果,该研究使用Illumina下一代测序技术对诊断微生物学实验室的临床样本进行病毒筛查。

Oxford Screening CSF and Respiratory samples ('OSCAR'): results of a pilot study to screen clinical samples from a diagnostic microbiology laboratory for viruses using Illumina next generation sequencing.

作者信息

Sharp Colin, Golubchik Tanya, Gregory William F, McNaughton Anna L, Gow Nicholas, Selvaratnam Mathyruban, Mirea Alina, Foster Dona, Andersson Monique, Klenerman Paul, Jeffery Katie, Matthews Philippa C

机构信息

The Roslin Institute, University of Edinburgh, Easter Bush, Midlothian, Edinburgh, EH25 9RG, Scotland, UK.

Edinburgh Genomics, Ashworth Laboratories, University of Edinburgh, Edinburgh, EH9 3FL, Scotland, UK.

出版信息

BMC Res Notes. 2018 Feb 9;11(1):120. doi: 10.1186/s13104-018-3234-8.

DOI:10.1186/s13104-018-3234-8
PMID:29426368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5810187/
Abstract

OBJECTIVES

There is increasing interest in the use of metagenomic (next generation sequencing, NGS) approaches for diagnosis of infection. We undertook a pilot study to screen samples submitted to a diagnostic microbiology laboratory in a UK teaching hospital using Illumina HiSeq. In the short-term, this small dataset provides insights into the virome of human respiratory and cerebrospinal fluid (CSF) samples. In the longer term, assimilating metagenomic data sets of this nature can inform optimization of laboratory and bioinformatic methods, and develop foundations for the interpretation of results in a clinical context. The project underpins a larger ongoing effort to develop NGS pipelines for diagnostic use.

DATA DESCRIPTION

Our data comprise a complete metagenomic dataset from 20 independent samples (10 CSF and 10 respiratory) submitted to the clinical microbiology laboratory for a large UK teaching hospital (Oxford University Hospitals NHS Foundation Trust). Sequences have been uploaded to the European Nucleotide Archive and are also presented as Krona plots through which the data can be interactively visualized. In the longer term, further optimization is required to better define sensitivity and specificity of this approach to clinical samples.

摘要

目的

使用宏基因组学(下一代测序,NGS)方法诊断感染越来越受到关注。我们进行了一项试点研究,使用Illumina HiSeq对提交给英国一家教学医院诊断微生物实验室的样本进行筛查。短期内,这个小数据集能让我们深入了解人类呼吸道和脑脊液(CSF)样本的病毒组。从长远来看,整合这类宏基因组数据集可为实验室和生物信息学方法的优化提供参考,并为在临床背景下解读结果奠定基础。该项目为正在进行的一项更大规模的开发用于诊断的NGS流程的工作提供了支持。

数据描述

我们的数据包括来自一家大型英国教学医院(牛津大学医院国民保健服务信托基金)临床微生物实验室提交的20个独立样本(10个脑脊液样本和10个呼吸道样本)的完整宏基因组数据集。序列已上传至欧洲核苷酸档案馆,并且还以科罗纳图的形式呈现,通过该图可以交互式地可视化数据。从长远来看,需要进一步优化以更好地确定这种方法对临床样本的敏感性和特异性。