Multiplexing droplet-based single cell RNA-sequencing using genetic barcodes
Updated September 30, 2021Here, we introduce an in-silico algorithm demuxlet that harnesses naturally occurring genetic variation in a pool of cells from unrelated individuals to discover the sample identity of each cell and identify droplets containing cells from two different individuals (doublets). These two capabilities enable a simple multiplexing design that increases single cell library construction throughput by experimental design where cells from genetically diverse samples are multiplexed and captured at 2-10x over standard workflows. We further demonstrate the utility of sample multiplexing by characterizing the interindividual variability in cell type-specific responses of ~15k PBMCs to interferon-beta, a potent cytokine. Our computational tool enables sample multiplexing of droplet-based single cell RNA-seq for large-scale studies of population variation and could be extended to other single cell datasets that incorporate natural or synthetic DNA barcodes.
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Atlas
Analysis Portals
NoneProject Label
DropletSequencingNaturalGeneticVariationSpecies
Homo sapiens
Sample Type
specimens
Anatomical Entity
blood
Organ Part
Unspecified
Selected Cell Types
peripheral blood mononuclear cells
Disease Status (Specimen)
lupus erythematosus
Disease Status (Donor)
lupus erythematosus
Development Stage
human adult stage
Library Construction Method
10x sequencing
Nucleic Acid Source
single cell
Paired End
trueFile Format
Cell Count Estimate
43.2kDonor Count
8