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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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Samuel G. Rodriques
Robert R. Stickels
Aleksandrina Goeva
Science
Harvard University
Massachusetts Institute of Technology
Massachusetts General Hospital
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Rodriques et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69d733b63f2a6ac123b8a57a — DOI: https://doi.org/10.1126/science.aaw1219