binnedCoverage | binnedCoverage |
computeZ | computeZ |
constructBedRanges | constructBedRanges |
countFinalRegions | countFinalRegions |
createGranges | createGranges |
cutGRangesPerChromosome | cutGRangesPerChromosome |
DEScan2 | DEScan2 |
divideEachSampleByChromosomes | divideEachSampleByChromosomes |
finalRegions | finalRegions |
findOverlapsOverSamples | findOverlapsOverSamples |
findPeaks | findPeaks |
fromSamplesToChrsGRangesList | fromSamplesToChrsGRangesList |
keepRelevantChrs | keepRelevantChrs |
readBamAsBed | readBamAsBed |
readBedFile | readBedFile |
readFilesAsGRangesList | readFilesAsGRangesList |
RleListToRleMatrix | RleListToRleMatrix |
saveGRangesAsBed | saveGRangesAsBed |
saveGRangesAsTsv | saveGRangesAsTsv |
setGRGenomeInfo | setGRGenomeInfo given a genome code (i.e. "mm9","mm10","hg19","hg38") retrieve the SeqInfo of that genome and assigns it to the input GRanges. Finally filters out those Infos not necessary to the GRanges. |