Package: CNViz 1.20.0
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_1.20.0.tar.gz
CNViz_1.20.0.zip(r-4.7-any)CNViz_1.20.0.zip(r-4.6-any)CNViz_1.20.0.zip(r-4.5-any)
CNViz_1.20.0.tgz(r-4.6-any)CNViz_1.20.0.tgz(r-4.5-any)
CNViz_1.20.0.tar.gz(r-4.7-any)CNViz_1.20.0.tar.gz(r-4.6-any)
CNViz_1.20.0.tgz(r-4.6-emscripten)
manual.pdf |manual.html✨
DESCRIPTION |NEWS
card.svg |card.png
CNViz/json (API)
| # Install 'CNViz' in R: |
| install.packages('CNViz', repos = c('https://bioc-release.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-1.21.0(bioc 3.24)CNViz-1.20.0(bioc 3.23)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
visualizationcopynumbervariationsequencingdnaseq
Last updated from:6081b50ed4 (on RELEASE_3_23). Checks:8 NOTE, 2 OK. Indexed: no.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| bioc-checks | NOTE | 233 | ||
| linux-devel-x86_64 | NOTE | 422 | ||
| source / vignettes | OK | 325 | ||
| linux-release-x86_64 | NOTE | 486 | ||
| macos-release-arm64 | NOTE | 241 | ||
| macos-oldrel-arm64 | NOTE | 261 | ||
| windows-devel | NOTE | 377 | ||
| windows-release | NOTE | 372 | ||
| windows-oldrel | NOTE | 346 | ||
| wasm-release | OK | 214 |
Exports:launchCNViz
Dependencies:abindAnnotationDbiAnnotationFilteraskpassbackportsbamsignalsbase64encbezierBHBiobaseBiocGenericsBiocIObiocmakeBiocParallelBiostringsbiovizBasebitbit64bitopsblobBSgenomebslibcachemcheckmatecigarillocliclustercn.mopscodetoolscolorspacecommonmarkCopyNumberPlotscpp11crayoncrosstalkcurldata.tableDBIDelayedArraydichromatdigestdir.expirydplyrDTensembldbevaluatefarverfastmapfilelockfontawesomeforeignformatRFormulafsfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2gluegridExtragtablehighrHmischtmlTablehtmltoolshtmlwidgetshttpuvhttrIRangesisobandjquerylibjsonlitekaryoploteRKEGGRESTknitrlabelinglambda.rlaterlatticelazyevallifecyclemagrittrMatrixMatrixGenericsmatrixStatsmemoisemimennetopensslotelpillarpkgconfigplotlypngpromisesProtGenericspurrrR6rappdirsRColorBrewerRcppRCurlregioneRrestfulrrhdf5rhdf5filtersRhdf5libRhtslibrjsonrlangrmarkdownrpartRsamtoolsRSQLiterstudioapirtracklayerS4ArraysS4VectorsS7sassscalesSeqinfoshinysnowsourcetoolsSparseArraystringistringrSummarizedExperimentsystibbletidyrtidyselecttinytexUCSC.utilsutf8VariantAnnotationvctrsviridisLitewithrxfunXMLxtableXVectoryaml
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 |
