Nuclei multiplexing with barcoded antibodies for single-nucleus genomics

被引:108
作者
Gaublomme, Jellert T. [1 ,7 ]
Li, Bo [1 ,2 ,3 ]
McCabe, Cristin [1 ]
Knecht, Abigail [1 ]
Yang, Yiming [2 ,3 ]
Drokhlyansky, Eugene [1 ]
Van Wittenberghe, Nicholas [1 ]
Waldman, Julia [1 ]
Dionne, Danielle [1 ]
Nguyen, Lan [1 ]
De Jager, Philip L. [4 ]
Yeung, Bertrand [5 ]
Zhao, Xinfang [5 ]
Habib, Naomi [1 ,8 ]
Rozenblatt-Rosen, Orit [1 ]
Regev, Aviv [1 ,6 ]
机构
[1] Broad Inst MIT & Harvard, Klarman Cell Observ, Cambridge, MA 02142 USA
[2] Massachusetts Gen Hosp, Div Rheumatol Allergy & Immunol, Ctr Immunol & Inflammatory Dis, Boston, MA 02129 USA
[3] Harvard Med Sch, Boston, MA 02129 USA
[4] Columbia Univ, Med Ctr, Ctr Translat & Computat Neuroimmunol, New York, NY 10019 USA
[5] BioLegend Inc, San Diego, CA 92121 USA
[6] MIT, Howard Hughes Med Inst, Koch Inst Integrat Canc Res, Dept Biol, Cambridge, MA 02139 USA
[7] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[8] Hebrew Univ Jerusalem, Edmond & Lily Safra Ctr Brain Sci, IL-9190401 Jerusalem, Israel
关键词
RNA-SEQ; DISCOVERY; FRAMEWORK;
D O I
10.1038/s41467-019-10756-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Single-nucleus RNA-seq (snRNA-seq) enables the interrogation of cellular states in complex tissues that are challenging to dissociate or are frozen, and opens the way to human genetics studies, clinical trials, and precise cell atlases of large organs. However, such applications are currently limited by batch effects, processing, and costs. Here, we present an approach for multiplexing snRNA-seq, using sample-barcoded antibodies to uniquely label nuclei from distinct samples. Comparing human brain cortex samples profiled with or without hashing antibodies, we demonstrate that nucleus hashing does not significantly alter recovered profiles. We develop DemuxEM, a computational tool that detects inter-sample multiplets and assigns singlets to their sample of origin, and validate its accuracy using sex-specific gene expression, species-mixing and natural genetic variation. Our approach will facilitate tissue atlases of isogenic model organisms or from multiple biopsies or longitudinal samples of one donor, and large-scale perturbation screens.
引用
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页数:8
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