{"title":"Next Generation DNA Sequencing Technologies","authors":"Kelly Sarton","doi":"10.35248/0974-8369.21.13.E102","DOIUrl":null,"url":null,"abstract":"Copyright: 2021 © Sarton K. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised genomic research. In contrast, the previous Sanger sequencing technology, used to decipher the human genome, required over a decade to deliver the final draft. Although in genome research NGS has mostly superseded conventional Sanger sequencing, it has not yet translated into routine clinical practice. The aim of this article is to review the potential applications of NGS in paediatrics.","PeriodicalId":90454,"journal":{"name":"Biology and medicine (Aligarh)","volume":"13 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology and medicine (Aligarh)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/0974-8369.21.13.E102","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
下一代DNA测序技术
版权所有:2021©Sarton K.这是一篇根据知识共享署名许可条款发布的开放获取文章,该许可允许在任何媒体上不受限制地使用,分发和复制,前提是原始作品被适当引用。下一代测序(NGS),大规模平行测序或深度测序是描述一种DNA测序技术的相关术语,它已经彻底改变了基因组研究。相比之下,之前用于破译人类基因组的桑格测序技术需要十多年的时间才能完成最终草案。尽管在基因组研究中,NGS在很大程度上取代了传统的Sanger测序,但它尚未转化为常规临床实践。本文的目的是回顾NGS在儿科的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。