{"title":"Recent enhancements in SSCP","authors":"Kenshi Hayashi","doi":"10.1016/S1050-3862(98)00017-5","DOIUrl":null,"url":null,"abstract":"<div><p>High sensitivity, robustness and scalability are the three criteria which influence whether techniques for rapid mutation detection will be used in the future. PCR-SSCP, one of the most popular methods for detecting mutation, especially in the field of medical genetics, is being improved (1) to efficiently detect mutations in long stretches of PCR products; (2) to simplify data interpretation by removing PCR artifacts and (3) to minimize human involvement in the process of mutation detection by a simple post-PCR fluorescence labeling followed by separation using automated DNA sequencers.</p></div>","PeriodicalId":77142,"journal":{"name":"Genetic analysis, techniques and applications","volume":"14 5","pages":"Pages 193-196"},"PeriodicalIF":0.0000,"publicationDate":"1999-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1050-3862(98)00017-5","citationCount":"32","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetic analysis, techniques and applications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1050386298000175","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 32
Abstract
High sensitivity, robustness and scalability are the three criteria which influence whether techniques for rapid mutation detection will be used in the future. PCR-SSCP, one of the most popular methods for detecting mutation, especially in the field of medical genetics, is being improved (1) to efficiently detect mutations in long stretches of PCR products; (2) to simplify data interpretation by removing PCR artifacts and (3) to minimize human involvement in the process of mutation detection by a simple post-PCR fluorescence labeling followed by separation using automated DNA sequencers.