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Next-Generation Sequencing Technology to Identify Minimal Residual Disease in Lymphoid Malignancies.
Kotrova, Michaela; Darzentas, Nikos; Pott, Christiane; Brüggemann, Monika.
Afiliação
  • Kotrova M; Unit for Hematological Diagnostics, Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Darzentas N; Unit for Hematological Diagnostics, Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Pott C; Unit for Hematological Diagnostics, Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Brüggemann M; Unit for Hematological Diagnostics, Medical Department II, University Hospital Schleswig-Holstein, Kiel, Germany. m.brueggemann@med2.uni-kiel.de.
Methods Mol Biol ; 2185: 95-111, 2021.
Article em En | MEDLINE | ID: mdl-33165845
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes de Imunoglobulinas / Receptores de Antígenos de Linfócitos T / Rearranjo Gênico / Neoplasias Hematológicas / Sequenciamento de Nucleotídeos em Larga Escala / Transtornos Linfoproliferativos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes de Imunoglobulinas / Receptores de Antígenos de Linfócitos T / Rearranjo Gênico / Neoplasias Hematológicas / Sequenciamento de Nucleotídeos em Larga Escala / Transtornos Linfoproliferativos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article