计算机科学
素描
可视化
聚类分析
计算生物学
转录组
层次聚类
资源(消歧)
数据集成
数据科学
数据挖掘
生物
机器学习
基因
基因表达
计算机网络
生物化学
算法
作者
Brian Hie,Hyunghoon Cho,Benjamin DeMeo,Bryan Bryson,Bonnie Berger
出处
期刊:Cell systems
[Elsevier]
日期:2019-06-01
卷期号:8 (6): 483-493.e7
被引量:109
标识
DOI:10.1016/j.cels.2019.05.003
摘要
Large-scale single-cell RNA sequencing (scRNA-seq) studies that profile hundreds of thousands of cells are becoming increasingly common, overwhelming existing analysis pipelines. Here, we describe how to enhance and accelerate single-cell data analysis by summarizing the transcriptomic heterogeneity within a dataset using a small subset of cells, which we refer to as a geometric sketch. Our sketches provide more comprehensive visualization of transcriptional diversity, capture rare cell types with high sensitivity, and reveal biological cell types via clustering. Our sketch of umbilical cord blood cells uncovers a rare subpopulation of inflammatory macrophages, which we experimentally validated. The construction of our sketches is extremely fast, which enabled us to accelerate other crucial resource-intensive tasks, such as scRNA-seq data integration, while maintaining accuracy. We anticipate our algorithm will become an increasingly essential step when sharing and analyzing the rapidly growing volume of scRNA-seq data and help enable the democratization of single-cell omics.
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