Package: DEScan2 1.27.0
DEScan2: Differential Enrichment Scan 2
Integrated peak and differential caller, specifically designed for broad epigenomic signals.
Authors:
DEScan2_1.27.0.tar.gz
DEScan2_1.27.0.zip(r-4.5)DEScan2_1.27.0.zip(r-4.4)DEScan2_1.27.0.zip(r-4.3)
DEScan2_1.27.0.tgz(r-4.4-x86_64)DEScan2_1.27.0.tgz(r-4.4-arm64)DEScan2_1.27.0.tgz(r-4.3-x86_64)DEScan2_1.27.0.tgz(r-4.3-arm64)
DEScan2_1.27.0.tar.gz(r-4.5-noble)DEScan2_1.27.0.tar.gz(r-4.4-noble)
DEScan2_1.27.0.tgz(r-4.4-emscripten)DEScan2_1.27.0.tgz(r-4.3-emscripten)
DEScan2.pdf |DEScan2.html✨
DEScan2/json (API)
NEWS
# Install 'DEScan2' in R: |
install.packages('DEScan2', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
On BioConductor:DEScan2-1.27.0(bioc 3.21)DEScan2-1.26.0(bioc 3.20)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
immunooncologypeakdetectionepigeneticssoftwaresequencingcoveragecpp
Last updated 2 months agofrom:b34d6d07e9. Checks:OK: 1 WARNING: 8. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Nov 29 2024 |
R-4.5-win-x86_64 | WARNING | Nov 29 2024 |
R-4.5-linux-x86_64 | WARNING | Nov 29 2024 |
R-4.4-win-x86_64 | WARNING | Nov 29 2024 |
R-4.4-mac-x86_64 | WARNING | Nov 29 2024 |
R-4.4-mac-aarch64 | WARNING | Nov 29 2024 |
R-4.3-win-x86_64 | WARNING | Nov 29 2024 |
R-4.3-mac-x86_64 | WARNING | Nov 29 2024 |
R-4.3-mac-aarch64 | WARNING | Nov 29 2024 |
Exports:binnedCoverageconstructBedRangescountFinalRegionscreateGrangescutGRangesPerChromosomedivideEachSampleByChromosomesfinalRegionsfindOverlapsOverSamplesfindPeaksfromSamplesToChrsGRangesListkeepRelevantChrsreadBamAsBedreadBedFilereadFilesAsGRangesListRleListToRleMatrixsaveGRangesAsBedsaveGRangesAsTsvsetGRGenomeInfo
Dependencies:abindAnnotationDbiAnnotationFilteraskpassBHBiobaseBiocFileCacheBiocGenericsBiocIOBiocParallelbiomaRtBiostringsbitbit64bitopsblobBSgenomecachemChIPpeakAnnoclicodetoolscolorspacecpp11crayoncurldata.tableDBIdbplyrDelayedArraydigestdplyrensembldbfansifarverfastmapfilelockformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2gluegraphgtablehmshttrhttr2InteractionSetIRangesisobandjsonliteKEGGRESTlabelinglambda.rlatticelazyevallifecyclemagrittrMASSMatrixMatrixGenericsmatrixStatsmemoisemgcvmimemulttestmunsellnlmeopensslpillarpkgconfigplogrplyrpngprettyunitsprogressProtGenericspurrrpwalignR6rappdirsRBGLRColorBrewerRcppRcppArmadilloRcppThreadRCurlregioneRrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorsscalessnowSparseArraystringistringrSummarizedExperimentsurvivalsystibbletidyrtidyselectUCSC.utilsuniversalmotifutf8vctrsVennDiagramviridisLitewithrXMLxml2XVectoryamlzlibbioc
Readme and manuals
Help Manual
Help page | Topics |
---|---|
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 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. | setGRGenomeInfo |