Slide-seq is a technology which enables transcriptome-wide measurements with 10-micron spatial resolution by transferring RNA from tissue sections onto a surface covered in DNA-barcoded beads with known positions and inferring the locations of RNA using a sequencing-by-ligation strategy. We obtained the Slide-seq dataset collected on the mouse cerebellum from Broad Institute’s single-cell repository (https://singlecell.broadinstitute.org/single_cell/) with ID SCP354. We used the file “Puck_180430_6” which contains 18,671 genes measured on 25,551 beads with known spatial location information. The bead size is approaching the size of mammalian cells (10 microns), though each bead may overlap with multiple cells. After filtering out mitochondrial genes and genes that are not expressed on any bead, we analyzed a final set of 17,729 genes on 25,551 beads. The data is highly sparse with 99.46% entries being 0 (Additional file 1: Table S1).
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