首页> 外国专利> PCR sequencing method based on DNA molecular tag technology and DNA incomplete fragmentation technology and HLA genotyping method using the same

PCR sequencing method based on DNA molecular tag technology and DNA incomplete fragmentation technology and HLA genotyping method using the same

机译:基于DNA分子标签技术和DNA不完全断裂技术的PCR测序方法以及使用其的HLA基因分型方法

摘要

The invention provides a PCR sequencing method, wherein the combination of primer indexes, DNA incomplete shearing strategy and the second generation sequencing technique (Paired-End sequencing technique) can make the length of PCR products that can be sequenced by a sequencer longer than the maximum sequencing length of the sequencer whilst making full use of the characteristics of the second generation sequencing technique such as high throughput and low cost, thereby greatly broadening its applicable scope. In addition, the present invention also provides primer indexes for the PCR sequencing method and the use of the method in genotyping, particularly in HLA analysis, and also provides the PCR primers used, particularly the PCR primers for HLA-A, B, HLA-C and HLA-DQB1 gene.
机译:本发明提供了一种PCR测序方法,其中引物索引,DNA不完全剪切策略和第二代测序技术(Paired-End测序技术)的组合可以使可被测序仪测序的PCR产物的长度比最大的长。在充分利用第二代测序技术的特点(例如高通量和低成本)的同时,实现测序仪的测序长度,从而大大拓宽了其适用范围。另外,本发明还提供了用于PCR测序方法的引物索引,以及该方法在基因分型中,特别是在HLA分析中的用途,并且还提供了所使用的PCR引物,特别是用于HLA-A,B,HLA-的PCR引物。 C和HLA-DQB1基因。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

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