生物
转录组
T细胞受体
效应器
细胞
T细胞
单细胞分析
细胞生物学
计算生物学
核糖核酸
遗传学
分子生物学
基因
基因表达
免疫系统
作者
Michael J. T. Stubbington,Tapio Lönnberg,Valentina Proserpio,Simon Clare,Anneliese O. Speak,Gordon Dougan,Sarah A. Teichmann
出处
期刊:Nature Methods
[Springer Nature]
日期:2016-03-07
卷期号:13 (4): 329-332
被引量:403
摘要
The TraCeR tool extracts full-length, paired T cell receptor sequences from single-cell RNA-sequencing data from T lymphocytes, enabling a combination of clonotype and functional analysis. We developed TraCeR, a computational method to reconstruct full-length, paired T cell receptor (TCR) sequences from T lymphocyte single-cell RNA sequence data. TraCeR links T cell specificity with functional response by revealing clonal relationships between cells alongside their transcriptional profiles. We found that T cell clonotypes in a mouse Salmonella infection model span early activated CD4+ T cells as well as mature effector and memory cells.
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