# chromVAR 0.99.1 Updates to vignettes. # chromVAR 0.99.1 Changes in reponse to Bioconductor review: * Removed deprecated snake_case functions * Internal changes to make code neater, less prone to problems # chromVAR 0.99.0 First version submitted to Bioconductor # chromVAR 0.4.7 Made it mandatory to provide genome for some functions, rather than defaulting to hg19. Allow usage of FaFile or DNAStringSet instead of BSgenome for genome input. # chromVAR 0.4.2 ChromVAR is a package for determining variation in chromatin accessibility across sets of peaks sharing a common genomic annotations. Designed primarily for single-cell or sparse chromatin accessibility data, e.g. from scATAC-seq or sparse bulk ATAC or DNAse-seq experiments.