Package: BaalChIP 1.33.0
BaalChIP: BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes
The package offers functions to process multiple ChIP-seq BAM files and detect allele-specific events. Computes allele counts at individual variants (SNPs/SNVs), implements extensive QC steps to remove problematic variants, and utilizes a bayesian framework to identify statistically significant allele- specific events. BaalChIP is able to account for copy number differences between the two alleles, a known phenotypical feature of cancer samples.
Authors:
BaalChIP_1.33.0.tar.gz
BaalChIP_1.33.0.zip(r-4.5)BaalChIP_1.33.0.zip(r-4.4)
BaalChIP_1.33.0.tar.gz(r-4.5-noble)BaalChIP_1.33.0.tar.gz(r-4.4-noble)
BaalChIP_1.33.0.tgz(r-4.4-emscripten)
BaalChIP.pdf |BaalChIP.html✨
BaalChIP/json (API)
NEWS
# Install 'BaalChIP' in R: |
install.packages('BaalChIP', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
- BaalObject - BaalObject example dataset
- ENCODEexample - ENCODEexample example dataset
- FAIREexample - FAIREexample example dataset
- UniqueMappability50bp_hg19 - Genomic regions of unique mappability
- blacklist_hg19 - Blacklisted genomic regions
- pickrell2011cov1_hg19 - Genomic regions of collapsed repeats
On BioConductor:BaalChIP-1.31.0(bioc 3.20)BaalChIP-1.30.0(bioc 3.19)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
softwarechipseqbayesiansequencing
Last updated 23 days agofrom:6f46c6902a. Checks:OK: 1 WARNING: 3. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Oct 30 2024 |
R-4.5-win | WARNING | Oct 30 2024 |
R-4.5-linux | WARNING | Oct 30 2024 |
R-4.4-win | WARNING | Oct 30 2024 |
Exports:adjustmentBaalPlotalleleCountsBaalChIPBaalChIP.getBaalChIP.reportBaalChIP.runfilter1allelefilterIntbiasgetASBmergePerGroupplotQCplotSimulQCfiltersummaryASBsummaryQC
Dependencies:abindaskpassbackportsBHBiobaseBiocGenericsBiocParallelBiostringsbitopsbootbroomclicodacodetoolscolorspacecowplotcpp11crayoncurlDelayedArrayDerivdoBydoParalleldplyrfansifarverforeachformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicRangesggplot2gluegtablehttrIRangesisobanditeratorsjsonlitelabelinglambda.rlatticelifecyclemagrittrMASSMatrixMatrixGenericsmatrixStatsmgcvmicrobenchmarkmimemodelrmunsellnlmeopensslpillarpkgconfigplyrpurrrR6RColorBrewerRcppreshape2RhtslibrlangRsamtoolsS4ArraysS4VectorsscalessnowSparseArraystringistringrSummarizedExperimentsystibbletidyrtidyselectUCSC.utilsutf8vctrsviridisLitewithrXVectorzlibbioc
Readme and manuals
Help Manual
Help page | Topics |
---|---|
Method adjustmentBaalPlot | adjustmentBaalPlot adjustmentBaalPlot,BaalChIP-method |
Method alleleCounts | alleleCounts alleleCounts,BaalChIP-method |
BaalChIP-class | BaalChIP |
Method BaalChIP.get | BaalChIP.get BaalChIP.get,BaalChIP-method |
Method BaalChIP.report | BaalChIP.report BaalChIP.report,BaalChIP-method |
Method BaalChIP.run | BaalChIP.run BaalChIP.run,BaalChIP-method |
BaalObject example dataset | BaalObject |
Blacklisted genomic regions | blacklist_hg19 |
ENCODEexample example dataset | ENCODEexample |
FAIREexample example dataset | FAIREexample |
Method filter1allele | filter1allele filter1allele,BaalChIP-method |
Method filterIntbias | filterIntbias filterIntbias,BaalChIP-method |
Method getASB | getASB getASB,BaalChIP-method |
Method mergePerGroup | mergePerGroup mergePerGroup,BaalChIP-method |
Genomic regions of collapsed repeats | pickrell2011cov1_hg19 |
Method plotQC | plotQC plotQC,BaalChIP-method |
Method plotSimul | plotSimul plotSimul,BaalChIP-method |
Method QCfilter | QCfilter QCfilter,BaalChIP-method |
Method summaryASB | summaryASB summaryASB,BaalChIP-method |
Method summaryQC | summaryQC summaryQC,BaalChIP-method |
Genomic regions of unique mappability | UniqueMappability50bp_hg19 |