首页> 美国卫生研究院文献>Journal of Biomolecular Techniques : JBT >A New Sequencing Primer and Workflow Increase 5 Resolution and Throughput on HLA Sequencing
【2h】

A New Sequencing Primer and Workflow Increase 5 Resolution and Throughput on HLA Sequencing

机译:新的测序引物和工作流程提高了HLA测序的5分辨率和吞吐量

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

High quality and high accuracy are the hallmarks of Sanger resequencing projects. We have developed a new sequencing primer and workflow that improves 5' sequence resolution, increases throughput, and reduces hands-on time. The novel sequencing primer chemistry produces high quality bases from base 1 on POP-7TM polymer that previously only could be resolved on the slower POP-6TM polymer. The new primer chemistry and workflow also eliminates the need for a separate PCR clean-up step. These improvements reduce the entire workflow from PCR to finished sequence data to under 5 hours, compared to 8 hours for the standard workflow. We used our enhanced sequencing primer and workflow to investigate feasibility on Human Leukocyte Antigen (HLA) polymorphisms on twelve DNA samples by using the Invitrogen SeCore® HLA-DRB1 primer set and Group Specific Sequencing Primers. Sequencing reactions generated with the traditional sequencing primer and with the new sequencing primer were electrophoresed on Applied Biosystems 3500xl Genetic Analyzer using POP-7TM polymer. For each sequencing primer, we compared 5' resolution and basecalling accuracy and quality. On average the traditional primers produced high quality readable bases by base 25 after the sequencing primer while the new primers produced high quality bases by base 5, and by base 1 in many cases. Because of improved resolution, basecalling accuracy was increased. This simplified process without a separate PCR clean-up step reduced the overall workflow time by 40%. For HLA genes, obtaining readable sequence within 5 bases of the primer offers improved polymorphism detection and more efficient use of allele specific sequencing primers for heterozygous ambiguity resolution. In conclusion, the novel primer chemistry and workflow generates data superior in quality relative to other currently used solutions and offers significant time savings as well. Specific applications of this product are under development and not intended for clinical use.
机译:高质量和高精度是Sanger重测序项目的标志。我们开发了一种新的测序引物和工作流程,可改善5'序列分辨率,增加通量并减少动手时间。新颖的测序引物化学方法可从POP-7TM聚合物的碱基1生成高质量的碱基,以前只能在较慢的POP-6TM聚合物上进行拆分。新的引物化学和工作流程还消除了对单独的PCR纯化步骤的需要。与标准工作流程的8个小时相比,这些改进将从PCR到最终序列数据的整个工作流程减少到5小时以内。我们使用增强的测序引物和工作流程,通过使用InvitrogenSeCore®HLA-DRB1引物组和组特异性测序引物,研究了十二种DNA样品在人类白细胞抗原(HLA)多态性方面的可行性。使用POP-7TM聚合物在Applied Biosystems 3500xl基因分析仪上对传统测序引物和新测序引物产生的测序反应进行电泳。对于每种测序引物,我们比较了5'分辨率和碱基检出的准确性和质量。平均而言,传统引物以测序引物之后的25个碱基为基础产生高质量的可读碱基,而新引物以5个碱基和在许多情况下以1个碱基产生高质量的碱基。由于提高了分辨率,提高了碱基检出的准确性。这种简化的过程无需单独的PCR清理步骤,可将整个工作流程时间减少40%。对于HLA基因,在引物的5个碱基内获得可读序列可改善多态性检测,并更有效地使用等位基因特异性测序引物来解决杂合性歧义问题。总之,相对于当前使用的其他解决方案,新颖的引物化学和工作流程可产生质量更高的数据,并且还可以节省大量时间。该产品的特定应用正在开发中,并不打算用于临床。

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