Code used to analyze the single-nuclei multiome dataset generated for the manuscript "Cognitive rejuvenation through partial reprogramming of engram cells"
0_multiome_objs.R: create a Seurat objects from Cell Ranger ARC outputs of different samples.1_merge.R: merge all samples into a single Seurat object2_QC_labelling.Rmd: RNA and ATAC QC filtering. Dimensionality reduction and clustering. Labelling of engram+ cells. Save RNA and ATAC objects.3_ATAC_1_process.Rmd: ATAC data processing, dimensionality reduction and clustering.3_ATAC_2_peak.R: ATAC peak calling for each annotated cell type and group using MACS23_ATAC_3_1_DA.R: Differential Accessibility Analysis.3_ATAC_3_2_DA.Rmd: Differential Accessibility Analysis plotting and downstream analyses3_ATAC_4_min_footprint.R: ATAC footprinting.3_ATAC_5_min_motifs.Rmd: ATAC motif enrichment analysis and plotting.3_ATAC_6_LinkPeaks.R: Signac Peak linking to genes in the dataset3_RNA_1_composition.Rmd: cell types visualization and compositional analysis3_RNA_2_DE.Rmd: Differential expression analysis3_RNA_3_GSEA.Rmd: Gene Set Enrichment Analysis3_RNA_3_identity.Rmd: Identity score comparison between groups3_RNA_4_pseudotime.Rmd: Monocle pseudotime analysis based on engram and AD DEGs3_RNA_5_CHEA3.Rmd: TF enrichment analysis of downregulated genes4_integration.Rmd: Integration analyses, including RNA-ATAC correlationsscCODA.py: compositional analysis using ths scCODA package
The sequencing data analyzed here is deposited in the Gene Expression Omnibus repository, with the series record GSE276656.
The transcriptional landscapes from Figure S7 can be visualized here.