Cell
Volume 177, Issue 7, 13 June 2019, Pages 1873-1887.e17
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Single-Cell Multi-omic Integration Compares and Contrasts Features of Brain Cell Identity

https://doi.org/10.1016/j.cell.2019.05.006Get rights and content
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Highlights

  • Shared and dataset-specific metagene factors enable single-cell data integration

  • LIGER reveals inter-individual differences in bed nucleus and substantia nigra cells

  • Integration of in situ and dissociated scRNA-seq maps cell types in space

  • Joint definition of cortical cell types from single-cell RNA and epigenome profiles

Summary

Defining cell types requires integrating diverse single-cell measurements from multiple experiments and biological contexts. To flexibly model single-cell datasets, we developed LIGER, an algorithm that delineates shared and dataset-specific features of cell identity. We applied it to four diverse and challenging analyses of human and mouse brain cells. First, we defined region-specific and sexually dimorphic gene expression in the mouse bed nucleus of the stria terminalis. Second, we analyzed expression in the human substantia nigra, comparing cell states in specific donors and relating cell types to those in the mouse. Third, we integrated in situ and single-cell expression data to spatially locate fine subtypes of cells present in the mouse frontal cortex. Finally, we jointly defined mouse cortical cell types using single-cell RNA-seq and DNA methylation profiles, revealing putative mechanisms of cell-type-specific epigenomic regulation. Integrative analyses using LIGER promise to accelerate investigations of cell-type definition, gene regulation, and disease states.

Keywords

single-cell genomics
data integration
bed nucleus of the stria terminalis
substantia nigra

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3

Present address: University of Michigan, Department of Computational Medicine and Bioinformatics, 100 Washtenaw Avenue, Ann Arbor, MI, USA

4

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