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      Slide-seq: A scalable technology for measuring genome-wide expression at high spatial resolution.

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          Abstract

          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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          Author and article information

          Journal
          Science
          Science (New York, N.Y.)
          American Association for the Advancement of Science (AAAS)
          1095-9203
          0036-8075
          Mar 29 2019
          : 363
          : 6434
          Affiliations
          [1 ] Department of Physics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
          [2 ] MIT Media Lab, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
          [3 ] Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
          [4 ] Graduate School of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.
          [5 ] Division of Medical Science, Harvard Medical School, Boston, MA 02115, USA.
          [6 ] Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA. chenf@broadinstitute.org emacosko@broadinstitute.org.
          [7 ] Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
          Article
          NIHMS1036108 363/6434/1463
          10.1126/science.aaw1219
          6927209
          30923225
          e81db009-36c9-4cc5-9603-537db078fc90
          History

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