基因表达
小脑
基因
计算生物学
核糖核酸
生物
RNA序列
电池类型
基因组
可扩展性
DNA测序
细胞
神经科学
转录组
计算机科学
遗传学
数据库
作者
Samuel G. Rodriques,Robert R. Stickels,Aleksandrina Goeva,Caroline Martin,Evan Murray,Charles Vanderburg,Joshua D. Welch,Linlin M. Chen,Fei Chen,Evan Z. Macosko
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-03-28
卷期号:363 (6434): 1463-1467
被引量:1854
标识
DOI:10.1126/science.aaw1219
摘要
Spatial positions of cells in tissues strongly influence function, yet a high-throughput, genome-wide readout of gene expression with cellular resolution is lacking. We developed Slide-seq, a method for transferring RNA from tissue sections onto a surface covered in DNA-barcoded beads with known positions, allowing the locations of the RNA to be inferred by sequencing. Using Slide-seq, we localized cell types identified by single-cell RNA sequencing datasets within the cerebellum and hippocampus, characterized spatial gene expression patterns in the Purkinje layer of mouse cerebellum, and defined the temporal evolution of cell type-specific responses in a mouse model of traumatic brain injury. These studies highlight how Slide-seq provides a scalable method for obtaining spatially resolved gene expression data at resolutions comparable to the sizes of individual cells.
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