Single-Cell Sequencing of Brain Cell Transcriptomes and Epigenomes

被引:161
作者
Armand, Ethan J. [1 ]
Li, Junhao [1 ]
Xie, Fangming [2 ]
Luo, Chongyuan [3 ]
Mukamel, Eran A. [1 ]
机构
[1] Univ Calif San Diego, Dept Cognit Sci, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Phys, La Jolla, CA 92037 USA
[3] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
关键词
GENOME-WIDE EXPRESSION; NUCLEUS RNA-SEQ; DNA METHYLATION; CHROMATIN ACCESSIBILITY; GENE-EXPRESSION; NEURONAL SUBTYPES; DIVERSITY; HETEROGENEITY; ARCHITECTURE; LANDSCAPE;
D O I
10.1016/j.neuron.2020.12.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Single-cell sequencing technologies, including transcriptomic and epigenomic assays, are transforming our understanding of the cellular building blocks of neural circuits. By directly measuring multiple molecular signatures in thousands to millions of individual cells, single-cell sequencing methods can comprehensively characterize the diversity of brain cell types. These measurements uncover gene regulatory mechanisms that shape cellular identity and provide insight into developmental and evolutionary relationships between brain cell populations. Single-cell sequencing data can aid the design of tools for targeted functional studies of brain circuit components, linking molecular signatures with anatomy, connectivity, morphology, and physiology. Here, we discuss the fundamental principles of single-cell transcriptome and epigenome sequencing, integrative computational analysis of the data, and key applications in neuroscience.
引用
收藏
页码:11 / 26
页数:16
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