# load the methylation data
data(methylationDataList)
#load the DMRs in CG context. These DMRs were computed with minGap = 200.
data(DMRsNoiseFilterCG)
#retrive the number of reads in CHH context in WT
DMRsNoiseFilterCGreadsCHH <- analyseReadsInsideRegionsForCondition(
                             DMRsNoiseFilterCG[1:10],
                             methylationDataList[["WT"]], context = "CHH",
                             label = "WT")
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