Slide-seq: A scalable technology for measuring genome-wide expression at high spatial resolution.
Samuel G RodriquesRobert R StickelsAleksandrina GoevaCaroline A MartinEvan MurrayCharles R VanderburgJoshua WelchLinlin M ChenFei ChenEvan Z MacoskoPublished in: Science (New York, N.Y.) (2019)
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.
Keyphrases
- single cell
- gene expression
- rna seq
- genome wide
- dna methylation
- high throughput
- induced apoptosis
- traumatic brain injury
- mouse model
- cell cycle arrest
- single molecule
- poor prognosis
- cell death
- endoplasmic reticulum stress
- oxidative stress
- electronic health record
- signaling pathway
- bone marrow
- cell proliferation
- big data
- cognitive impairment
- brain injury
- cell free
- circulating tumor
- circulating tumor cells
- data analysis