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长读纳米孔测序在常规诊断中对人类白细胞抗原 I 类分型的验证。

Long-Read Nanopore Sequencing Validated for Human Leukocyte Antigen Class I Typing in Routine Diagnostics.

机构信息

Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Center, Maastricht, the Netherlands.

Transplantation Immunology, Tissue Typing Laboratory, Maastricht University Medical Center, Maastricht, the Netherlands.

出版信息

J Mol Diagn. 2020 Jul;22(7):912-919. doi: 10.1016/j.jmoldx.2020.04.001. Epub 2020 Apr 14.

Abstract

Matching of human leukocyte antigen (HLA) gene polymorphisms by high-resolution DNA sequence analysis is the gold standard for determining compatibility between patient and donor for hematopoietic stem cell transplantation. Single-molecule sequencing (PacBio or MinION) is a newest (third) generation sequencing approach. MinION is a nanopore sequencing platform, which provides long targeted DNA sequences. The long reads provide unambiguous phasing, but the initial high error profile prevented its use in high-impact applications, such as HLA typing for HLA matching of donor and recipient in the transplantation setting. Ongoing developments on instrumentation and basecalling software have improved the per-base accuracy of 1D nanopore reads tremendously. In the current study, two validation panels of samples covering 70 of the 71 known HLA class I allele groups were used to compare third field sequences obtained by MinION, with Sanger sequence-based typing showing a 100% concordance between both data sets. In addition, the first validation panel was used to set the acceptance criteria for the use of MinION in a routine setting. The acceptance criteria were subsequently confirmed with the second validation panel. In summary, the present study describes validation and implementation of nanopore sequencing HLA class I typing method and illustrates that nanopore sequencing technology has advanced to a point where it can be used in routine diagnostics with high accuracy.

摘要

通过高分辨率 DNA 序列分析匹配人类白细胞抗原(HLA)基因多态性是确定造血干细胞移植患者与供体之间相容性的金标准。单分子测序(PacBio 或 MinION)是最新的(第三代)测序方法。MinION 是一种纳米孔测序平台,可提供长靶向 DNA 序列。长读长提供了明确的相位,但最初的高错误率阻止了它在高影响的应用中使用,例如在移植环境中为供体和受者的 HLA 配型进行 HLA 匹配。仪器和碱基调用软件的持续开发极大地提高了 1D 纳米孔读数的每个碱基的准确性。在本研究中,使用涵盖 71 个已知 HLA Ⅰ类等位基因组的 70 个样本的两个验证面板来比较 MinION 获得的第三组序列,与基于 Sanger 测序的分型相比,两组数据之间具有 100%的一致性。此外,第一验证面板用于为 MinION 在常规环境中的使用设定接受标准。随后使用第二个验证面板确认了该接受标准。总之,本研究描述了纳米孔测序 HLA Ⅰ类分型方法的验证和实施,并说明了纳米孔测序技术已经发展到可以高精度地用于常规诊断的地步。

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