Spatially mapped single-cell chromatin accessibility

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作者
Casey A. Thornton
Ryan M. Mulqueen
Kristof A. Torkenczy
Andrew Nishida
Eve G. Lowenstein
Andrew J. Fields
Frank J. Steemers
Wenri Zhang
Heather L. McConnell
Randy L. Woltjer
Anusha Mishra
Kevin M. Wright
Andrew C. Adey
机构
[1] Oregon Health & Science University,Molecular and Medical Genetics
[2] Illumina Inc.,Anesthesiology and Peri
[3] Oregon Health & Science University,Operative Medicine
[4] Oregon Health & Science University,Jungers Center for Neurosciences Research, Department of Neurology
[5] Oregon Health & Science University,Department of Pathology
[6] Oregon Health & Science University,Knight Cardiovascular Institute
[7] Oregon Health & Science University,The Vollum Institute
[8] CEDAR,Knight Cancer Institute
[9] Oregon Health & Science University,undefined
[10] Oregon Health & Science University,undefined
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摘要
High-throughput single-cell epigenomic assays can resolve cell type heterogeneity in complex tissues, however, spatial orientation is lost. Here, we present single-cell combinatorial indexing on Microbiopsies Assigned to Positions for the Assay for Transposase Accessible Chromatin, or sciMAP-ATAC, as a method for highly scalable, spatially resolved, single-cell profiling of chromatin states. sciMAP-ATAC produces data of equivalent quality to non-spatial sci-ATAC and retains the positional information of each cell within a 214 micron cubic region, with up to hundreds of tracked positions in a single experiment. We apply sciMAP-ATAC to assess cortical lamination in the adult mouse primary somatosensory cortex and in the human primary visual cortex, where we produce spatial trajectories and integrate our data with non-spatial single-nucleus RNA and other chromatin accessibility single-cell datasets. Finally, we characterize the spatially progressive nature of cerebral ischemic infarction in the mouse brain using a model of transient middle cerebral artery occlusion.
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