Accuracy of Next Generation Sequencing Platforms.

Edward J Fox, Kate S Reid-Bayliss, Mary J Emond, Lawrence A Loeb
{"title":"Accuracy of Next Generation Sequencing Platforms.","authors":"Edward J Fox,&nbsp;Kate S Reid-Bayliss,&nbsp;Mary J Emond,&nbsp;Lawrence A Loeb","doi":"10.4172/jngsa.1000106","DOIUrl":null,"url":null,"abstract":"<p><p>Next-generation DNA sequencing has revolutionized genomic studies and is driving the implementation of precision diagnostics. The ability of these technologies to disentangle sequence heterogeneity, however, is limited by their relatively high error rates. A Several single molecule barcoding strategies have been propose to reduce the overall error frequency. A Duplex Sequencing additionally exploits the fact that DNA is double-strand, with one strand reciprocally encoding the sequence information of its complement, and can eliminate nearly all sequencing errors by comparing the sequence of individually tagged amplicons derived from one strand of DNA with that of its complementary strand. This method reduces errors to fewer than one per ten million nucleotides sequenced.</p>","PeriodicalId":90934,"journal":{"name":"Next generation, sequencing & applications","volume":"1 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/jngsa.1000106","citationCount":"221","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next generation, sequencing & applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/jngsa.1000106","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 221

Abstract

Next-generation DNA sequencing has revolutionized genomic studies and is driving the implementation of precision diagnostics. The ability of these technologies to disentangle sequence heterogeneity, however, is limited by their relatively high error rates. A Several single molecule barcoding strategies have been propose to reduce the overall error frequency. A Duplex Sequencing additionally exploits the fact that DNA is double-strand, with one strand reciprocally encoding the sequence information of its complement, and can eliminate nearly all sequencing errors by comparing the sequence of individually tagged amplicons derived from one strand of DNA with that of its complementary strand. This method reduces errors to fewer than one per ten million nucleotides sequenced.

Abstract Image

下一代测序平台的准确性。
下一代DNA测序已经彻底改变了基因组研究,并正在推动精确诊断的实施。然而,这些技术解开序列异质性的能力受到其相对较高的错误率的限制。已经提出了几种单分子条形码策略来降低总体错误频率。双工测序还利用了DNA是双链的事实,其中一条链相互编码其补体的序列信息,并且可以通过比较来自一条DNA链的单独标记的扩增子序列与其互补链的扩增子序列来消除几乎所有的测序错误。这种方法将误差降低到少于1 / 1000万个核苷酸测序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信