{"title":"NEBNext Direct: A Novel, Rapid, Hybridization-Based Approach for the Capture and Library Conversion of Genomic Regions of Interest","authors":"Amy B. Emerman, Sarah K. Bowman, Andrew Barry, Noa Henig, Kruti M. Patel, Andrew F. Gardner, Cynthia L. Hendrickson","doi":"10.1002/cpmb.39","DOIUrl":null,"url":null,"abstract":"<p>Next-generation sequencing (NGS) is a powerful tool for genomic studies, translational research, and clinical diagnostics that enables the detection of single nucleotide polymorphisms, insertions and deletions, copy number variations, and other genetic variations. Target enrichment technologies improve the efficiency of NGS by only sequencing regions of interest, which reduces sequencing costs while increasing coverage of the selected targets. Here we present NEBNext Direct<sup>®</sup>, a hybridization-based, target-enrichment approach that addresses many of the shortcomings of traditional target-enrichment methods. This approach features a simple, 7-hr workflow that uses enzymatic removal of off-target sequences to achieve a high specificity for regions of interest. Additionally, unique molecular identifiers are incorporated for the identification and filtering of PCR duplicates. The same protocol can be used across a wide range of input amounts, input types, and panel sizes, enabling NEBNext Direct to be broadly applicable across a wide variety of research and diagnostic needs. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10734,"journal":{"name":"Current Protocols in Molecular Biology","volume":"119 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmb.39","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmb.39","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 18
Abstract
Next-generation sequencing (NGS) is a powerful tool for genomic studies, translational research, and clinical diagnostics that enables the detection of single nucleotide polymorphisms, insertions and deletions, copy number variations, and other genetic variations. Target enrichment technologies improve the efficiency of NGS by only sequencing regions of interest, which reduces sequencing costs while increasing coverage of the selected targets. Here we present NEBNext Direct®, a hybridization-based, target-enrichment approach that addresses many of the shortcomings of traditional target-enrichment methods. This approach features a simple, 7-hr workflow that uses enzymatic removal of off-target sequences to achieve a high specificity for regions of interest. Additionally, unique molecular identifiers are incorporated for the identification and filtering of PCR duplicates. The same protocol can be used across a wide range of input amounts, input types, and panel sizes, enabling NEBNext Direct to be broadly applicable across a wide variety of research and diagnostic needs. © 2017 by John Wiley & Sons, Inc.
NEBNext Direct:一种新颖,快速,基于杂交的方法,用于捕获和感兴趣的基因组区域的文库转换
下一代测序(NGS)是基因组研究、转化研究和临床诊断的强大工具,可以检测单核苷酸多态性、插入和缺失、拷贝数变异和其他遗传变异。目标富集技术通过只测序感兴趣的区域来提高NGS的效率,从而降低测序成本,同时增加所选目标的覆盖范围。在这里,我们提出了NEBNext Direct®,一种基于杂交的目标富集方法,解决了传统目标富集方法的许多缺点。这种方法的特点是一个简单的,7小时的工作流程,使用酶去除脱靶序列来实现对感兴趣区域的高特异性。此外,独特的分子标识符被纳入PCR重复的识别和过滤。相同的协议可用于广泛的输入量,输入类型和面板尺寸,使NEBNext Direct广泛适用于各种研究和诊断需求。©2017 by John Wiley &儿子,Inc。
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