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下一代测序技术在淋巴恶性肿瘤微小残留病灶中的应用。

Next-Generation Sequencing Technology to Identify Minimal Residual Disease in Lymphoid Malignancies.

机构信息

Unit for Hematological Diagnostics, Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany.

出版信息

Methods Mol Biol. 2021;2185:95-111. doi: 10.1007/978-1-0716-0810-4_7.

Abstract

Next-generation sequencing (NGS) of immunoglobulin (IG) and T cell receptor (TR) rearrangements represents a modern alternative to classical RQ-PCR-based minimal residual disease (MRD) detection. The same primer sets and conditions can be used for all patients, which is undoubtedly one of the most important benefits of NGS, not only reducing the labor required to perform the analysis but also enabling the assay to comply with the upcoming EU IVD regulation. So far, only one standardized academic protocol for this task has been published, developed, and validated within the EuroClonality-NGS working group. In this chapter we describe the materials and methods for amplicon library preparation for sequencing on Illumina MiSeq, and the bioinformatic pipeline for this protocol.

摘要

下一代测序(NGS)的免疫球蛋白(IG)和 T 细胞受体(TR)重排代表了一种现代的替代经典基于 RQ-PCR 的微小残留病(MRD)检测方法。相同的引物集和条件可用于所有患者,这无疑是 NGS 的最重要优势之一,不仅减少了进行分析所需的劳动力,而且还使检测符合即将出台的欧盟体外诊断法规。到目前为止,只有一个标准化的学术方案在 EuroClonality-NGS 工作组内得到了发表、开发和验证。在本章中,我们描述了用于 Illumina MiSeq 测序的扩增子文库制备的材料和方法,以及该方案的生物信息学流程。

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