Determine variation in chromatin accessibility across sets of annotations or peaks. Designed primarily for single-cell or sparse chromatin accessibility data, e.g. from scATAC-seq or sparse bulk ATAC or DNAse-seq experiments.
Package details |
|
---|---|
Bioconductor views | GeneRegulation ImmunoOncology Sequencing SingleCell |
Maintainer | |
License | MIT + file LICENSE |
Version | 1.5.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.