首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Novel Method for Genotyping Hepatitis B Virus on the Basis of TaqMan Real-Time PCR
【2h】

Novel Method for Genotyping Hepatitis B Virus on the Basis of TaqMan Real-Time PCR

机译:基于TaqMan实时PCR的乙型肝炎病毒基因分型的新方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Chronic infection with hepatitis B virus (HBV) is an important cause of cirrhosis and cancer of the liver. HBV is currently classified into eight genotypes, A to H. Accumulated evidence shows that the genotype influences both the clinical course of infection and the response to treatment. We describe a new method for genotyping based on TaqMan real-time PCR, which identifies all HBV genotypes without post-PCR processing. In this assay, each sample is processed in four multiplex real-time PCRs, each targeting two or three genotype-specific segments of HBV. By analyzing 185 samples representing all genotypes and different proportions of genotype mixtures, we could validate high accuracy of the assay. We conclude that this new assay represents a significant advancement for both diagnostics and clinical research because it is accurate, practical, and based on a technique that is well established in many virological laboratories.
机译:乙型肝炎病毒(HBV)的慢性感染是肝硬化和肝癌的重要原因。 HBV目前分为8种基因型,从A到H。积累的证据表明,该基因型既影响感染的临床过程,也影响对治疗的反应。我们描述了一种基于TaqMan实时PCR进行基因分型的新方法,该方法无需PCR后即可识别所有HBV基因型。在该测定中,每个样品均在四个多重实时PCR中进行处理,每个PCR均针对两个或三个HBV基因型特异性片段。通过分析代表所有基因型和不同比例的基因型混合物的185个样品,我们可以验证测定的高精度。我们得出的结论是,这种新方法代表了诊断和临床研究的重大进步,因为它准确,实用并且基于许多病毒学实验室中已建立的技术。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号