• 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

UltraSEQ,一个基于信息的临床宏基因组学及其他领域的通用生物信息学平台。

UltraSEQ, a Universal Bioinformatic Platform for Information-Based Clinical Metagenomics and Beyond.

机构信息

Battelle Memorial Institute, Columbus, Ohio, USA.

出版信息

Microbiol Spectr. 2023 Jun 15;11(3):e0416022. doi: 10.1128/spectrum.04160-22. Epub 2023 Apr 11.

DOI:10.1128/spectrum.04160-22
PMID:37039637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10269449/
Abstract

Applied metagenomics is a powerful emerging capability enabling the untargeted detection of pathogens, and its application in clinical diagnostics promises to alleviate the limitations of current targeted assays. While metagenomics offers a hypothesis-free approach to identify any pathogen, including unculturable and potentially novel pathogens, its application in clinical diagnostics has so far been limited by workflow-specific requirements, computational constraints, and lengthy expert review requirements. To address these challenges, we developed UltraSEQ, a first-of-its-kind accurate and scalable metagenomic bioinformatic tool for potential clinical diagnostics and biosurveillance utility. Here, we present the results of the evaluation of our novel UltraSEQ pipeline using an -synthesized metagenome, mock microbial community data sets, and publicly available clinical data sets from samples of different infection types, including both short-read and long-read sequencing data. Our results show that UltraSEQ successfully detected all expected species across the tree of life in the sample and detected all 10 bacterial and fungal species in the mock microbial community data set. For clinical data sets, even without requiring data set-specific configuration setting changes, background sample subtraction, or prior sample information, UltraSEQ achieved an overall accuracy of 91%. Furthermore, as an initial demonstration with a limited patient sample set, we show UltraSEQ's ability to provide antibiotic resistance and virulence factor genotypes that are consistent with phenotypic results. Taken together, the above-described results demonstrate that the UltraSEQ platform offers a transformative approach for microbial and metagenomic sample characterization, employing a biologically informed detection logic, deep metadata, and a flexible system architecture for the classification and characterization of taxonomic origin, gene function, and user-defined functions, including disease-causing infections. Traditional clinical microbiology-based diagnostic tests rely on targeted methods that can detect only one to a few preselected organisms or slow, culture-based methods. Although widely used today, these methods have several limitations, resulting in rates of cases of an unknown etiology of infection of >50% for several disease types. Massive developments in sequencing technologies have made it possible to apply metagenomic methods to clinical diagnostics, but current offerings are limited to a specific disease type or sequencer workflow and/or require laboratory-specific controls. The limitations associated with current clinical metagenomic offerings result from the fact that the backend bioinformatic pipelines are optimized for the specific parameters described above, resulting in an excess of unmaintained, redundant, and niche tools that lack standardization and explainable outputs. In this paper, we demonstrate that UltraSEQ uses a novel, information-based approach that enables accurate, evidence-based predictions for diagnosis as well as the functional characterization of a sample.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/d8195724762d/spectrum.04160-22-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/9748326500dd/spectrum.04160-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/36cf789fafd6/spectrum.04160-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/5333b1007bf0/spectrum.04160-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/d8195724762d/spectrum.04160-22-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/9748326500dd/spectrum.04160-22-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/36cf789fafd6/spectrum.04160-22-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/5333b1007bf0/spectrum.04160-22-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ac/10269449/d8195724762d/spectrum.04160-22-f004.jpg
摘要

应用宏基因组学是一种强大的新兴能力,可实现对病原体的非靶向检测,其在临床诊断中的应用有望缓解当前靶向检测方法的局限性。宏基因组学提供了一种无需假设即可识别任何病原体的方法,包括无法培养和潜在的新型病原体,但它在临床诊断中的应用迄今为止受到工作流程特定要求、计算限制和冗长的专家审查要求的限制。为了解决这些挑战,我们开发了 UltraSEQ,这是一种用于潜在临床诊断和生物监测应用的首创、准确且可扩展的宏基因组生物信息学工具。在这里,我们展示了使用合成宏基因组、模拟微生物群落数据集以及来自不同感染类型样本的公开可用临床数据集评估我们新型 UltraSEQ 管道的结果,包括短读长和长读长测序数据。我们的结果表明,UltraSEQ 成功地在样本中检测到了生命之树上的所有预期物种,并在模拟微生物群落数据集中检测到了所有 10 种细菌和真菌物种。对于临床数据集,即使不需要数据集特定的配置更改、背景样本扣除或事先的样本信息,UltraSEQ 也实现了 91%的总体准确性。此外,作为对有限患者样本集的初步演示,我们展示了 UltraSEQ 提供抗生素耐药性和毒力因子基因型的能力,这些基因型与表型结果一致。综上所述,上述结果表明,UltraSEQ 平台为微生物和宏基因组样本表征提供了一种变革性方法,采用生物信息学检测逻辑、深入的元数据和灵活的系统架构,用于分类和表征分类起源、基因功能和用户定义的功能,包括致病感染。传统的基于临床微生物学的诊断测试依赖于靶向方法,只能检测一个到几个预先选择的生物体或缓慢的、基于培养的方法。尽管这些方法今天被广泛使用,但它们有几个局限性,导致几种疾病类型的感染病因不明的病例率超过 50%。测序技术的巨大发展使得将宏基因组方法应用于临床诊断成为可能,但目前的产品仅限于特定的疾病类型或测序器工作流程,并且/或者需要实验室特定的对照。当前临床宏基因组产品的局限性源于后端生物信息学管道针对上述特定参数进行了优化的事实,导致了过多未维护、冗余和利基工具,这些工具缺乏标准化和可解释的输出。在本文中,我们证明了 UltraSEQ 使用一种新颖的基于信息的方法,能够为诊断以及样本的功能表征提供准确、基于证据的预测。

相似文献

1
UltraSEQ, a Universal Bioinformatic Platform for Information-Based Clinical Metagenomics and Beyond.UltraSEQ,一个基于信息的临床宏基因组学及其他领域的通用生物信息学平台。
Microbiol Spectr. 2023 Jun 15;11(3):e0416022. doi: 10.1128/spectrum.04160-22. Epub 2023 Apr 11.
2
MinION™ nanopore sequencing of environmental metagenomes: a synthetic approach.环境宏基因组的MinION™纳米孔测序:一种合成方法。
Gigascience. 2017 Mar 1;6(3):1-10. doi: 10.1093/gigascience/gix007.
3
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.
4
Species classifier choice is a key consideration when analysing low-complexity food microbiome data.在分析低复杂度食品微生物组数据时,物种分类器的选择是一个关键考虑因素。
Microbiome. 2018 Mar 20;6(1):50. doi: 10.1186/s40168-018-0437-0.
5
Bioinformatic Pipeline for Profiling Foodborne Bacterial Ecology and Resistome from Short-Read Metagenomics.基于短读宏基因组学的食源性病原体细菌生态与抗药组学分析的生物信息学流程
Methods Mol Biol. 2025;2852:289-309. doi: 10.1007/978-1-0716-4100-2_19.
6
Freshwater monitoring by nanopore sequencing.利用纳米孔测序进行淡水监测。
Elife. 2021 Jan 19;10:e61504. doi: 10.7554/eLife.61504.
7
Validation of a Metagenomic Next-Generation Sequencing Assay for Lower Respiratory Pathogen Detection.宏基因组下一代测序检测下呼吸道病原体的验证。
Microbiol Spectr. 2023 Feb 14;11(1):e0381222. doi: 10.1128/spectrum.03812-22. Epub 2022 Dec 12.
8
Intestinal microbiota domination under extreme selective pressures characterized by metagenomic read cloud sequencing and assembly.肠道微生物群落在具有宏基因组读段云测序和组装特征的极端选择压力下占主导地位。
BMC Bioinformatics. 2019 Dec 2;20(Suppl 16):585. doi: 10.1186/s12859-019-3073-1.
9
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.
10
Metagenomic Next-Generation Sequencing of Nasopharyngeal Specimens Collected from Confirmed and Suspect COVID-19 Patients.对确诊和疑似 COVID-19 患者的鼻咽拭子标本进行宏基因组下一代测序。
mBio. 2020 Nov 20;11(6):e01969-20. doi: 10.1128/mBio.01969-20.

引用本文的文献

1
Inter-tool analysis of a NIST dataset for assessing baseline nucleic acid sequence screening.用于评估基线核酸序列筛查的美国国家标准与技术研究院数据集的工具间分析。
bioRxiv. 2025 Jun 1:2025.05.30.655379. doi: 10.1101/2025.05.30.655379.
2
Progress and Prospects for a Nucleic Acid Screening Test Set.核酸筛查检测套装的进展与前景
Appl Biosaf. 2024 Sep 18;29(3):133-141. doi: 10.1089/apb.2023.0033. eCollection 2024 Sep.
3
A Sensitivity Study for Interpreting Nucleic Acid Sequence Screening Regulatory and Guidance Documentation: Toward a Foundational Synthetic Nucleic Acid Sequence Screening Framework.

本文引用的文献

1
Function-based classification of hazardous biological sequences: Demonstration of a new paradigm for biohazard assessments.基于功能的有害生物序列分类:生物危害评估新范式的论证
Front Bioeng Biotechnol. 2022 Oct 7;10:979497. doi: 10.3389/fbioe.2022.979497. eCollection 2022.
2
K2Mem: Discovering Discriminative K-mers From Sequencing Data for Metagenomic Reads Classification.K2Mem:从测序数据中发现用于宏基因组读分类的判别 K- mers。
IEEE/ACM Trans Comput Biol Bioinform. 2022 Jan-Feb;19(1):220-229. doi: 10.1109/TCBB.2021.3117406. Epub 2022 Feb 3.
3
Benchmark of thirteen bioinformatic pipelines for metagenomic virus diagnostics using datasets from clinical samples.
解读核酸序列筛查监管与指导文件的敏感性研究:迈向基础合成核酸序列筛查框架
Appl Biosaf. 2024 Sep 18;29(3):150-158. doi: 10.1089/apb.2023.0026. eCollection 2024 Sep.
4
Non-Targeted RNA Sequencing: Towards the Development of Universal Clinical Diagnosis Methods for Human and Veterinary Infectious Diseases.非靶向RNA测序:迈向人类和兽医传染病通用临床诊断方法的发展
Vet Sci. 2024 May 26;11(6):239. doi: 10.3390/vetsci11060239.
基于临床样本数据集的宏基因组病毒诊断的十三种生物信息学分析流程的基准测试。
J Clin Virol. 2021 Aug;141:104908. doi: 10.1016/j.jcv.2021.104908. Epub 2021 Jul 8.
4
BugSeq: a highly accurate cloud platform for long-read metagenomic analyses.BugSeq:一个用于长读宏基因组分析的高度准确的云平台。
BMC Bioinformatics. 2021 Mar 25;22(1):160. doi: 10.1186/s12859-021-04089-5.
5
Data structures based on -mers for querying large collections of sequencing data sets.基于 - 元的序列数据集查询的大型数据集的数据结构。
Genome Res. 2021 Jan;31(1):1-12. doi: 10.1101/gr.260604.119. Epub 2020 Dec 16.
6
Metagenomic Sequencing To Detect Respiratory Viruses in Persons under Investigation for COVID-19.宏基因组测序在针对 COVID-19 进行调查的人群中检测呼吸道病毒。
J Clin Microbiol. 2020 Dec 17;59(1). doi: 10.1128/JCM.02142-20.
7
IDseq-An open source cloud-based pipeline and analysis service for metagenomic pathogen detection and monitoring.IDseq-一个用于宏基因组病原体检测和监测的开源基于云的管道和分析服务。
Gigascience. 2020 Oct 15;9(10). doi: 10.1093/gigascience/giaa111.
8
ResFinder 4.0 for predictions of phenotypes from genotypes.ResFinder 4.0 用于基因型到表型的预测。
J Antimicrob Chemother. 2020 Dec 1;75(12):3491-3500. doi: 10.1093/jac/dkaa345.
9
A metagenomics-based diagnostic approach for central nervous system infections in hospital acute care setting.基于宏基因组学的医院急性护理环境中中枢神经系统感染的诊断方法。
Sci Rep. 2020 Jul 8;10(1):11194. doi: 10.1038/s41598-020-68159-z.
10
Current challenges and best-practice protocols for microbiome analysis.当前微生物组分析面临的挑战和最佳实践方案。
Brief Bioinform. 2021 Jan 18;22(1):178-193. doi: 10.1093/bib/bbz155.