体细胞突变
B细胞受体
生物
剧目
互补决定区
断点群集区域
DNA测序
B细胞
深度测序
计算生物学
亲和力成熟
遗传学
体细胞
抗体
免疫球蛋白轻链
分子生物学
基因
基因组
物理
声学
作者
Jennifer Hom,Deepak Tomar,Christopher Tipton
出处
期刊:Methods in molecular biology
日期:2021-12-07
卷期号:: 231-241
被引量:4
标识
DOI:10.1007/978-1-0716-1944-5_16
摘要
Repertoire sequencing of B cells is the high-throughput profiling of B cell receptors (BCR) expressed on the surface of B cells and of immunoglobulins (Ig) expressed by antibody secreting cells. Each BCR/Ig transcript has a unique complementarity-determining region 3 (CDR3) sequence that can be used to identify and track individual B cell lymphocytes over time and throughout different compartments of the human body. B cell differentiation can be further tracked by assessing the point mutations acquired during affinity maturation via somatic hypermutation (SHM). Here we describe a method for high-throughput sequencing of the variable region of Ig heavy-chain transcripts for repertoire analysis of human B cells on the Illumina Miseq platform.
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