Package: DEScan2 1.33.0
DEScan2: Differential Enrichment Scan 2
Integrated peak and differential caller, specifically designed for broad epigenomic signals.
Authors:
DEScan2_1.33.0.tar.gz
DEScan2_1.33.0.zip(r-4.7)DEScan2_1.33.0.zip(r-4.6)DEScan2_1.31.0.zip(r-4.5)
DEScan2_1.33.0.tgz(r-4.6-x86_64)DEScan2_1.33.0.tgz(r-4.6-arm64)DEScan2_1.31.0.tgz(r-4.5-x86_64)DEScan2_1.31.0.tgz(r-4.5-arm64)
DEScan2_1.33.0.tar.gz(r-4.7-arm64)DEScan2_1.33.0.tar.gz(r-4.7-x86_64)DEScan2_1.33.0.tar.gz(r-4.6-arm64)DEScan2_1.33.0.tar.gz(r-4.6-x86_64)
DEScan2_1.33.0.tgz(r-4.6-emscripten)
manual.pdf |manual.html✨
card.svg |card.png
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:DEScan2-1.33.0(bioc 3.24)DEScan2-1.32.0(bioc 3.23)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
immunooncologypeakdetectionepigeneticssoftwaresequencingcoveragecpp
Last updated from:47c99148d9. Checks:1 ERROR, 5 NOTE, 2 OK, 3 WARNING, 3 FAIL. Indexed: yes.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| bioc-checks | ERROR | 287 | ||
| linux-devel-arm64 | NOTE | 499 | ||
| linux-devel-x86_64 | NOTE | 618 | ||
| source / vignettes | OK | 377 | ||
| linux-release-arm64 | WARNING | 458 | ||
| linux-release-x86_64 | NOTE | 603 | ||
| macos-release-arm64 | NOTE | 312 | ||
| macos-release-x86_64 | NOTE | 515 | ||
| macos-oldrel-arm64 | FAIL | 70 | ||
| macos-oldrel-x86_64 | FAIL | 177 | ||
| windows-devel | WARNING | 584 | ||
| windows-release | WARNING | 611 | ||
| windows-oldrel | FAIL | 101 | ||
| wasm-release | OK | 222 |
Exports:binnedCoverageconstructBedRangescountFinalRegionscreateGrangescutGRangesPerChromosomedivideEachSampleByChromosomesfinalRegionsfindOverlapsOverSamplesfindPeaksfromSamplesToChrsGRangesListkeepRelevantChrsreadBamAsBedreadBedFilereadFilesAsGRangesListRleListToRleMatrixsaveGRangesAsBedsaveGRangesAsTsvsetGRGenomeInfo
Dependencies:abindAnnotationDbiAnnotationFilteraskpassBHBiobaseBiocBaseUtilsBiocFileCacheBiocGenericsBiocIOBiocParallelbiomaRtBiostringsbitbit64bitopsblobBSgenomecachemChIPpeakAnnocigarilloclicodetoolscpp11crayoncurldata.tableDBIdbplyrDelayedArraydplyrensembldbfarverfastmapfilelockformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2gluegraphgtablehmshttrhttr2InteractionSetIRangesisobandjsonliteKEGGRESTlabelinglambda.rlatticelazyevallifecyclemagrittrMASSMatrixMatrixGenericsmatrixStatsmemoisemimemulttestopensslpillarpkgconfigplyrpngprettyunitsprogressProtGenericspurrrpwalignR6rappdirsRBGLRColorBrewerRcppRcppArmadilloRcppThreadRCurlregioneRrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorsS7scalesSeqinfosnowSparseArraystringistringrSummarizedExperimentsurvivalsystibbletidyrtidyselectUCSC.utilsuniversalmotifutf8vctrsVennDiagramviridisLitewithrXMLxml2XVectoryaml
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 |
