Slide-seq: A scalable technology for measuring genome-wide expression at high spatial resolution
Author(s) -
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
Publication year - 2019
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaw1219
Subject(s) - computational biology , gene expression , rna , biology , cerebellum , rna seq , gene , genome , cell type , scalability , dna sequencing , cell , transcriptome , genetics , computer science , neuroscience , database
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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