R/data.R
exampleOpenSignalMatrix_hg19.Rd
Preparation steps:
made a universe of regions by merging regions across cell types defined as opened in ENCODE
took bigwig files from ENCODE for individual cell types, merged replicates, filtered out blacklisted sites
evaluated the signal above regions defined by previous step
performed quantile normalization
subsetted it
data(exampleOpenSignalMatrix_hg19)
data.frame, rows represent whole selection of open chromatin regions across all cell types defined by ENCODE, columns are individual cell types and values are normalized open chromatin signal values.