• 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

基因组测序仪FLX系统——读长更长、应用更多、生物信息学简单直接且数据集更完整。

The Genome Sequencer FLX System--longer reads, more applications, straight forward bioinformatics and more complete data sets.

作者信息

Droege Marcus, Hill Brendon

机构信息

Roche Applied Science, Global Marketing, 82372 Penzberg, Germany.

出版信息

J Biotechnol. 2008 Aug 31;136(1-2):3-10. doi: 10.1016/j.jbiotec.2008.03.021. Epub 2008 Jun 21.

DOI:10.1016/j.jbiotec.2008.03.021
PMID:18616967
Abstract

The Genome Sequencer FLX System (GS FLX), powered by 454 Sequencing, is a next-generation DNA sequencing technology featuring a unique mix of long reads, exceptional accuracy, and ultra-high throughput. It has been proven to be the most versatile of all currently available next-generation sequencing technologies, supporting many high-profile studies in over seven applications categories. GS FLX users have pursued innovative research in de novo sequencing, re-sequencing of whole genomes and target DNA regions, metagenomics, and RNA analysis. 454 Sequencing is a powerful tool for human genetics research, having recently re-sequenced the genome of an individual human, currently re-sequencing the complete human exome and targeted genomic regions using the NimbleGen sequence capture process, and detected low-frequency somatic mutations linked to cancer.

摘要

由454测序技术驱动的基因组测序仪FLX系统(GS FLX)是一种新一代DNA测序技术,具有长读长、超高准确性和超高通量的独特组合。它已被证明是目前所有可用的新一代测序技术中用途最广泛的,支持超过七个应用类别的许多备受瞩目的研究。GS FLX用户已在从头测序、全基因组和目标DNA区域的重测序、宏基因组学及RNA分析方面开展了创新性研究。454测序技术是人类遗传学研究的强大工具,最近已对一个人的基因组进行了重测序,目前正在使用NimbleGen序列捕获方法对完整的人类外显子组和目标基因组区域进行重测序,并检测到了与癌症相关的低频体细胞突变。

相似文献

1
The Genome Sequencer FLX System--longer reads, more applications, straight forward bioinformatics and more complete data sets.基因组测序仪FLX系统——读长更长、应用更多、生物信息学简单直接且数据集更完整。
J Biotechnol. 2008 Aug 31;136(1-2):3-10. doi: 10.1016/j.jbiotec.2008.03.021. Epub 2008 Jun 21.
2
DraGnET: software for storing, managing and analyzing annotated draft genome sequence data.DraGnET:用于存储、管理和分析带注释的草图基因组序列数据的软件。
BMC Bioinformatics. 2010 Feb 22;11:100. doi: 10.1186/1471-2105-11-100.
3
Artificial duplicate reads in sequencing data of 454 Genome Sequencer FLX System.454 基因组测序仪测序数据中的人工重复读。
Acta Biochim Biophys Sin (Shanghai). 2011 Jun;43(6):496-500. doi: 10.1093/abbs/gmr030. Epub 2011 May 4.
4
Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing.用于下一代全外显子组和基因组测序的计算与生物信息学框架。
ScientificWorldJournal. 2013;2013:730210. doi: 10.1155/2013/730210. Epub 2013 Jan 13.
5
Using quality scores and longer reads improves accuracy of Solexa read mapping.使用质量得分和更长的读段可提高Solexa读段比对的准确性。
BMC Bioinformatics. 2008 Feb 28;9:128. doi: 10.1186/1471-2105-9-128.
6
Genomorama: genome visualization and analysis.基因组全景图:基因组可视化与分析
BMC Bioinformatics. 2007 Jun 14;8:204. doi: 10.1186/1471-2105-8-204.
7
CoVaCS: a consensus variant calling system.CoVaCS:一个共识变异调用系统。
BMC Genomics. 2018 Feb 5;19(1):120. doi: 10.1186/s12864-018-4508-1.
8
Mapping RNA-seq Reads with STAR.使用STAR对RNA测序读数进行比对
Curr Protoc Bioinformatics. 2015 Sep 3;51:11.14.1-11.14.19. doi: 10.1002/0471250953.bi1114s51.
9
Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads.单轮循环器:从短读长和长读长测序数据中解析细菌基因组组装结果
PLoS Comput Biol. 2017 Jun 8;13(6):e1005595. doi: 10.1371/journal.pcbi.1005595. eCollection 2017 Jun.
10
Automated querying of genome databases.基因组数据库的自动查询。
PLoS Comput Biol. 2007 Jan 26;3(1):e1. doi: 10.1371/journal.pcbi.0030001.

引用本文的文献

1
Bioinformatics Resources for Plant Abiotic Stress Responses: State of the Art and Opportunities in the Fast Evolving -Omics Era.植物非生物胁迫响应的生物信息学资源:快速发展的组学时代的现状与机遇
Plants (Basel). 2020 May 6;9(5):591. doi: 10.3390/plants9050591.
2
Probiotic Expressing a Nucleic Acid-Hydrolyzing Minibody (3D8 Scfv) Enhances Probiotic Activities in Mice Intestine as Revealed by Metagenomic Analyses.宏基因组分析显示,表达核酸水解微型抗体(3D8单链抗体片段)的益生菌增强了小鼠肠道中的益生菌活性。
Genes (Basel). 2018 May 29;9(6):276. doi: 10.3390/genes9060276.
3
Draft genome sequence of CLST isolated from the acidic hypersaline Gorbea salt flat in northern Chile.
从智利北部酸性高盐戈尔贝亚盐沼分离出的CLST的基因组序列草图。
Stand Genomic Sci. 2017 Dec 19;12:84. doi: 10.1186/s40793-017-0305-8. eCollection 2017.
4
Evolution of selective-sequencing approaches for virus discovery and virome analysis.病毒发现和病毒组分析中选择测序方法的演变。
Virus Res. 2017 Jul 15;239:172-179. doi: 10.1016/j.virusres.2017.06.005. Epub 2017 Jun 3.
5
Effects of Lead and Mercury on Sulfate-Reducing Bacterial Activity in a Biological Process for Flue Gas Desulfurization Wastewater Treatment.铅和汞对烟气脱硫废水生物处理过程中硫酸盐还原菌活性的影响
Sci Rep. 2016 Jul 26;6:30455. doi: 10.1038/srep30455.
6
Mineral Type and Solution Chemistry Affect the Structure and Composition of Actively Growing Bacterial Communities as Revealed by Bromodeoxyuridine Immunocapture and 16S rRNA Pyrosequencing.通过溴脱氧尿苷免疫捕获和16S rRNA焦磷酸测序揭示,矿物类型和溶液化学影响活跃生长的细菌群落的结构和组成。
Microb Ecol. 2016 Aug;72(2):428-42. doi: 10.1007/s00248-016-0774-0. Epub 2016 May 2.
7
Next-generation genotyping of hypervariable loci in many individuals of a non-model species: technical and theoretical implications.非模式物种众多个体中高变位点的新一代基因分型:技术与理论意义
BMC Genomics. 2016 Mar 8;17:204. doi: 10.1186/s12864-016-2503-y.
8
Draft genome sequence of chloride-tolerant Leptospirillum ferriphilum Sp-Cl from industrial bioleaching operations in northern Chile.来自智利北部工业生物浸出作业的耐氯嗜铁钩端螺旋菌Sp-Cl的基因组序列草图
Stand Genomic Sci. 2016 Feb 27;11:19. doi: 10.1186/s40793-016-0142-1. eCollection 2016.
9
Bacterial cellulose synthesis mechanism of facultative anaerobe Enterobacter sp. FY-07.兼性厌氧菌阴沟肠杆菌FY-07的细菌纤维素合成机制
Sci Rep. 2016 Feb 25;6:21863. doi: 10.1038/srep21863.
10
Nature and Extent of Genetic Diversity of Dengue Viruses Determined by 454 Pyrosequencing.通过454焦磷酸测序法测定登革病毒的遗传多样性的性质与程度
PLoS One. 2015 Nov 13;10(11):e0142473. doi: 10.1371/journal.pone.0142473. eCollection 2015.