Package: rvarsim 0.99.1
rvarsim: R/Bioconductor Variant Simulator with HGVS Notation
Simulates all possible single nucleotide variants (SNVs) across MANE Select transcripts including coding sequence (CDS), untranslated regions (UTRs), and canonical splice sites. Outputs variants in HGVS notation. Provides a comprehensive HGVS toolkit: parsing, syntactic and semantic validation, normalization (3' shifting, common affix trimming), format conversion (HGVS <-> VCF <-> SPDI), transcription mapping (genomic <-> coding), translation to protein consequence, backtranslation from protein to coding variants, variant extraction from sequence alignment, and liftover between genome assemblies.
Authors:
rvarsim_0.99.1.tar.gz
rvarsim_0.99.1.zip(r-4.7)rvarsim_0.99.1.zip(r-4.6)rvarsim_0.99.1.zip(r-4.5)
rvarsim_0.99.1.tgz(r-4.6-any)rvarsim_0.99.1.tgz(r-4.5-any)
rvarsim_0.99.1.tar.gz(r-4.7-any)rvarsim_0.99.1.tar.gz(r-4.6-any)
rvarsim_0.99.1.tgz(r-4.6-emscripten)
manual.pdf |manual.html✨
card.svg |card.png
rvarsim/json (API)
| # Install 'rvarsim' in R: |
| install.packages('rvarsim', repos = c('https://biocstaging.r-universe.dev', 'https://cloud.r-project.org')) |
Bug tracker:https://github.com/liu-sun/rvarsim/issues
geneticsvariantannotationsnpsequencingtranscriptionvariantdetectionalignmentnormalization
Last updated from:7b0d289ded. Checks:8 NOTE, 2 OK. Indexed: yes.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| bioc-checks | NOTE | 303 | ||
| linux-devel-x86_64 | NOTE | 496 | ||
| source / vignettes | OK | 371 | ||
| linux-release-x86_64 | NOTE | 447 | ||
| macos-release-arm64 | NOTE | 283 | ||
| macos-oldrel-arm64 | NOTE | 388 | ||
| windows-devel | NOTE | 377 | ||
| windows-release | NOTE | 371 | ||
| windows-oldrel | NOTE | 387 | ||
| wasm-release | OK | 266 |
Exports:backtranslate_hgvsc_to_gextract_hgvsfetch_mane_txdbformat_hgvsg_to_cgenerate_variantsget_transcript_structurehgvs_to_spdihgvs_to_vcfis_valid_hgvsliftover_c_hgvsliftover_hgvsnormalize_hgvsparse_hgvssimulate_variantsspdi_to_hgvstranscribe_hgvstranslate_hgvsvalidate_hgvsvcf_to_hgvs
Dependencies:abindAnnotationDbiAnnotationFilteraskpassBHBiobaseBiocBaseUtilsBiocGenericsBiocIOBiocParallelBiostringsbitbit64bitopsblobBSgenomecachemcigarilloclicodetoolscpp11crayoncurlDBIDelayedArrayensembldbfastmapformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomicAlignmentsGenomicFeaturesGenomicRangesgluehttrIRangesjsonliteKEGGRESTlambda.rlatticelazyevallifecycleMatrixMatrixGenericsmatrixStatsmemoisemimeopensslpkgconfigpngProtGenericsR6RCurlrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorsSeqinfosnowSparseArraySummarizedExperimentsysUCSC.utilsvctrsXMLXVectoryaml
