sciMET-cap: high-throughput single-cell methylation analysis with a reduced sequencing burden
Sonia N. Acharya, Ruth V. Nichols, Lauren Rylaarsdam, Brendan L. O’Connell, Theodore P. Braun, Andrew Adey
Abstract
DNA methylation is a key component of the mammalian epigenome, playing a regulatory role in development, disease, and other processes. Robust, high-throughput single-cell DNA methylation assays are now possible (sciMET); however, the genome-wide nature of DNA methylation results in a high sequencing burden per cell. Here, we leverage target enrichment with sciMET to capture sufficient information per cell for cell type assignment using substantially fewer sequence reads (sciMET-cap). Accumulated off-target coverage enables genome-wide differentially methylated region (DMR) calling for clusters with as few as 115 cells. We characterize sciMET-cap on human PBMCs and brain (middle frontal gyrus).