G&T-seq: parallel sequencing of single-cell genomes and transcriptomes

被引:535
作者
Macaulay, Iain C. [1 ]
Haerty, Wilfried [2 ]
Kumar, Parveen [3 ]
Li, Yang I. [2 ]
Hu, Tim Xiaoming [2 ]
Teng, Mabel J. [4 ]
Goolam, Mubeen [5 ]
Saurat, Nathalie [6 ]
Coupland, Paul [7 ]
Shirley, Lesley M. [7 ]
Smith, Miriam [7 ]
Van der Aa, Niels [3 ]
Banerjee, Ruby [8 ]
Ellis, Peter D. [7 ]
Quail, Michael A. [7 ]
Swerdlow, Harold P. [7 ]
Zernicka-Goetz, Magdalena [5 ]
Livesey, Frederick J. [6 ]
Ponting, Chris P. [1 ,2 ]
Voet, Thierry [1 ,3 ]
机构
[1] Wellcome Trust Sanger Inst, Sanger Inst, EBI Single Cell Genom Ctr, Hinxton, England
[2] Univ Oxford, Dept Physiol Anat & Genet, MRC Funct Genom Unit, Oxford, England
[3] Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium
[4] Wellcome Trust Sanger Inst, Canc Genome Project, Cambridge, England
[5] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[6] Univ Cambridge, Wellcome Trust Canc Res UK Gurdon Inst, Cambridge, England
[7] Wellcome Trust Sanger Inst, Sequencing R&D, Cambridge, England
[8] Wellcome Trust Sanger Inst, Cytogenet Core Facil, Cambridge, England
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
PLURIPOTENT STEM-CELLS; COPY-NUMBER VARIATION; RNA-SEQ; GENE; ALIGNMENT; TUMOR; IDENTIFICATION; INHIBITOR;
D O I
10.1038/nmeth.3370
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The simultaneous sequencing of a single cell's genome and transcriptome offers a powerful means to dissect genetic variation and its effect on gene expression. Here we describe G&T-seq, a method for separating and sequencing genomic DNA and full-length mRNA from single cells. By applying G&T-seq to over 220 single cells from mice and humans, we discovered cellular properties that could not be inferred from DNA or RNA sequencing alone.
引用
收藏
页码:519 / +
页数:7
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