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. 2022 Dec 9;13:7627. doi: 10.1038/s41467-022-35374-3

Fig. 1. sciMETv2 method and experimental design.

Fig. 1

a Molecular workflow for the sciMETv2 technologies. b Nucleosome disruption effectiveness as measured by raw transcription start site (TSS) enrichment. Tagmentation of intact nuclei preserves TSS enrichment which is ablated by nucleosome disruption in sciMET assays. For all boxplots, boxes indicate median, 25th and 75th percentiles with min and max lines as 1.5x interquartile range. c Experimental design for the human and mouse mixing experiments, the analysis workflow, and species alignment rates for a subset of the sequencing reads in order to determine doublet rates and identify species specific cell barcodes.