Suppr超能文献

使用基于Ion Torrent的二代测序技术对临床标本进行HLA基因分型。

HLA-genotyping of clinical specimens using Ion Torrent-based NGS.

作者信息

Barone Jonathan C, Saito Katsuyuki, Beutner Karl, Campo Maria, Dong Wei, Goswami Chirayu P, Johnson Erica S, Wang Zi-Xuan, Hsu Susan

机构信息

American Red Cross, 700 Spring Garden Street, Philadelphia, PA 19123, USA.

One Lambda, Inc., 21001 Kittridge Street, Canoga Park, CA 91303, USA.

出版信息

Hum Immunol. 2015 Dec;76(12):903-9. doi: 10.1016/j.humimm.2015.09.014. Epub 2015 Sep 28.

Abstract

We have evaluated and validated the NXType™ workflow (One Lambda, Inc.) and the accompanying TypeStream™ software on the Ion Torrent Next Generation Sequencing (NGS) platform using a comprehensive testing panel. The panel consisted of 285 genomic DNA (gDNA) samples derived from four major ethnic populations and contained 59 PT samples and 226 clinical specimens. The total number of alleles from the six loci interrogated by NGS was 3420. This validation panel provided a wide range of HLA sequence variations including many rare alleles, new variants and homozygous alleles. The NXType™ system (reagents and software) was able to correctly genotype the vast majority of these specimens. The concordance rate between SBT-derived genotypes and those generated by TypeStream™ auto-analysis ranged from 99.5% to 99.8% for the HLA-A, B, C, DRB1 and DQB1 loci, and was 98.9% for HLA-DPB1. A strategy for data review was developed that would allow correction of most of the few remaining typing errors. The entire NGS workflow from gDNA amplification to genotype assignment could be completed within 3 working days. Through this validation study, the limitations and shortcomings of the platform, specific assay system, and software algorithm were also revealed for further evaluation and improvement.

摘要

我们使用一个综合测试面板,在Ion Torrent下一代测序(NGS)平台上评估并验证了NXType™工作流程(One Lambda公司)及配套的TypeStream™软件。该测试面板由来自四个主要种族群体的285个基因组DNA(gDNA)样本组成,包含59个PT样本和226个临床标本。通过NGS检测的六个位点的等位基因总数为3420个。这个验证面板提供了广泛的HLA序列变异,包括许多罕见等位基因、新变异和纯合等位基因。NXType™系统(试剂和软件)能够对绝大多数这些标本进行正确的基因分型。对于HLA - A、B、C、DRB1和DQB1位点,基于序列特异性寡核苷酸探针技术(SBT)得到的基因型与TypeStream™自动分析生成的基因型之间的一致性率在99.5%至99.8%之间,对于HLA - DPB1位点则为98.9%。我们制定了一种数据审查策略,该策略能够纠正剩余的少数分型错误中的大多数。从gDNA扩增到基因型确定的整个NGS工作流程可以在3个工作日内完成。通过这项验证研究,该平台、特定检测系统和软件算法的局限性和缺点也被揭示出来,以供进一步评估和改进。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验