染色质
表观遗传学
计算生物学
可扩展性
单细胞分析
计算机科学
微流控
细胞
吞吐量
时间轴
生物
纳米技术
遗传学
数学
DNA甲基化
DNA
基因表达
材料科学
数据库
基因
电信
统计
无线
作者
Caleb A. Lareau,Fabiana M. Duarte,Jennifer G. Chew,Vinay K. Kartha,Zach D. Burkett,Andrew S. Kohlway,Dmitry Pokholok,Martin J. Aryee,Frank J. Steemers,Ronald Lebofsky,Jason Daniel Buenrostro
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2019-04-18
被引量:10
摘要
Abstract While recent technical advancements have facilitated the mapping of epigenomes at single-cell resolution, the throughput and quality of these methods have limited the widespread adoption of these technologies. Here, we describe a droplet microfluidics platform for single-cell assay for transposase accessible chromatin (scATAC-seq) for high-throughput single-cell profiling of chromatin accessibility. We use this approach for the unbiased discovery of cell types and regulatory elements within the mouse brain. Further, we extend the throughput of this approach by pairing combinatorial indexing with droplet microfluidics, enabling single-cell studies at a massive scale. With this approach, we measure chromatin accessibility across resting and stimulated human bone marrow derived cells to reveal changes in the cis - and trans- regulatory landscape across cell types and upon stimulation conditions at single-cell resolution. Altogether, we describe a total of 502,207 single-cell profiles, demonstrating the scalability and flexibility of this droplet-based platform.
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