Package: CNViz 1.15.0
CNViz: Copy Number Visualization
CNViz takes probe, gene, and segment-level log2 copy number ratios and launches a Shiny app to visualize your sample's copy number profile. You can also integrate loss of heterozygosity (LOH) and single nucleotide variant (SNV) data.
Authors:
CNViz_1.15.0.tar.gz
CNViz_1.15.0.zip(r-4.5)CNViz_1.15.0.zip(r-4.4)CNViz_1.15.0.zip(r-4.3)
CNViz_1.15.0.tgz(r-4.4-any)CNViz_1.15.0.tgz(r-4.3-any)
CNViz_1.15.0.tar.gz(r-4.5-noble)CNViz_1.15.0.tar.gz(r-4.4-noble)
CNViz_1.15.0.tgz(r-4.4-emscripten)CNViz_1.15.0.tgz(r-4.3-emscripten)
CNViz.pdf |CNViz.html✨
CNViz/json (API)
NEWS
# Install 'CNViz' in R: |
install.packages('CNViz', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
- gene_data - Gene data for vignette example
- meta_data - Metadata for vignette example
- probe_data - Probe data for vignette example
- segment_data - Segment data for vignette example
- variant_data - Variant data for vignette example
On BioConductor:CNViz-1.15.0(bioc 3.21)CNViz-1.14.0(bioc 3.20)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
visualizationcopynumbervariationsequencingdnaseq
Last updated 2 months agofrom:5bf989fea4. Checks:OK: 1 NOTE: 6. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Dec 17 2024 |
R-4.5-win | NOTE | Dec 17 2024 |
R-4.5-linux | NOTE | Dec 17 2024 |
R-4.4-win | NOTE | Dec 17 2024 |
R-4.4-mac | NOTE | Dec 17 2024 |
R-4.3-win | NOTE | Dec 17 2024 |
R-4.3-mac | NOTE | Dec 17 2024 |
Exports:launchCNViz
Dependencies:abindAnnotationDbiAnnotationFilteraskpassbackportsbamsignalsbase64encbezierBHBiobaseBiocGenericsBiocIOBiocParallelBiostringsbiovizBasebitbit64bitopsblobBSgenomebslibcachemcheckmatecliclustercn.mopscodetoolscolorspacecommonmarkCopyNumberPlotscpp11crayoncrosstalkcurldata.tableDBIDelayedArraydichromatdigestdplyrDTensembldbevaluatefansifarverfastmapfontawesomeforeignformatRFormulafsfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2gluegridExtragtablehighrHmischtmlTablehtmltoolshtmlwidgetshttpuvhttrIRangesisobandjquerylibjsonlitekaryoploteRKEGGRESTknitrlabelinglambda.rlaterlatticelazyevallifecyclemagrittrMASSMatrixMatrixGenericsmatrixStatsmemoisemgcvmimemunsellnlmennetopensslpillarpkgconfigplogrplotlypngpromisesProtGenericspurrrR6rappdirsRColorBrewerRcppRCurlregioneRrestfulrrhdf5rhdf5filtersRhdf5libRhtslibrjsonrlangrmarkdownrpartRsamtoolsRSQLiterstudioapirtracklayerS4ArraysS4VectorssassscalesshinysnowsourcetoolsSparseArraystringistringrSummarizedExperimentsystibbletidyrtidyselecttinytexUCSC.utilsutf8VariantAnnotationvctrsviridisviridisLitewithrxfunXMLxtableXVectoryamlzlibbioc
Readme and manuals
Help Manual
Help page | Topics |
---|---|
Data from 2018 TCGA studies from cBioPortal | all_tcga2018_data |
Names of 2018 TCGA studies from cBioPortal | cbio_studies |
Genomic locations of cytoband labels | cytoband_data |
Gene data for vignette example | gene_data |
Launches CNViz, a shiny app to visualize your sample's copy number data. | launchCNViz |
Metadata for vignette example | meta_data |
Probe data for vignette example | probe_data |
Segment data for vignette example | segment_data |
Variant data for vignette example | variant_data |