Package: mitoClone2 1.19.0

mitoClone2: Clonal Population Identification in Single-Cell RNA-Seq Data using Mitochondrial and Somatic Mutations
This package primarily identifies variants in mitochondrial genomes from BAM alignment files. It filters these variants to remove RNA editing events then estimates their evolutionary relationship (i.e. their phylogenetic tree) and groups single cells into clones. It also visualizes the mutations and providing additional genomic context.
Authors:
mitoClone2_1.19.0.tar.gz
mitoClone2_1.19.0.zip(r-4.7)mitoClone2_1.19.0.zip(r-4.6)mitoClone2_1.19.0.zip(r-4.5)
mitoClone2_1.19.0.tgz(r-4.6-arm64)mitoClone2_1.19.0.tgz(r-4.5-arm64)
mitoClone2_1.19.0.tar.gz(r-4.7-arm64)mitoClone2_1.19.0.tar.gz(r-4.7-x86_64)mitoClone2_1.19.0.tar.gz(r-4.6-arm64)mitoClone2_1.19.0.tar.gz(r-4.6-x86_64)
manual.pdf |manual.html✨
card.svg |card.png
mitoClone2/json (API)
NEWS
| # Install 'mitoClone2' in R: |
| install.packages('mitoClone2', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
Bug tracker:https://github.com/benstory/mitoclone2/issues
On BioConductor:mitoClone2-1.19.0(bioc 3.24)mitoClone2-1.18.0(bioc 3.23)
annotationdataimportgeneticssnpsoftwaresinglecellalignmentcurlbzip2xz-utilszlibcpp
Last updated from:179a14fa42. Checks:1 ERROR, 7 NOTE, 1 OK, 2 WARNING, 3 FAIL. Indexed: yes.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| bioc-checks | ERROR | 227 | ||
| linux-devel-arm64 | NOTE | 397 | ||
| linux-devel-x86_64 | NOTE | 479 | ||
| source / vignettes | OK | 486 | ||
| linux-release-arm64 | NOTE | 384 | ||
| linux-release-x86_64 | NOTE | 498 | ||
| macos-release-arm64 | WARNING | 285 | ||
| macos-release-x86_64 | FAIL | 216 | ||
| macos-oldrel-arm64 | WARNING | 275 | ||
| macos-oldrel-x86_64 | FAIL | 192 | ||
| windows-devel | NOTE | 538 | ||
| windows-release | NOTE | 475 | ||
| windows-oldrel | NOTE | 460 | ||
| wasm-release | FAIL | 171 |
Exports:bam2R_10xbaseCountsFromBamListclusterMetaclonesexclusionlistsgetAlleleCountgetCloneLikelihoodgetMut2ClonegetVarsCandidatemitoPlotmut2GRmutationCallsFromCohortmutationCallsFromExclusionlistmutationCallsFromMatrixoverwriteMetaclonesplotClonespredictCellAssignmentpullcountsVarsquick_clusterremoveWindowsetVarsCandidatevarClustervireoFit
Dependencies:abindAnnotationDbiaskpassBHBiobaseBiocBaseUtilsBiocGenericsBiocIOBiocParallelBiostringsbitbit64bitopsblobBSgenomecachemcigarilloclicodetoolscpp11crayoncurlDBIdeepSNVDelayedArrayfarverfastmapformatRfutile.loggerfutile.optionsgenericsGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2gluegtablehttrIRangesisobandjsonliteKEGGRESTlabelinglambda.rlatticelifecyclemagrittrMatrixMatrixGenericsmatrixStatsmemoisemimeopensslpheatmappkgconfigplyrpngR6RColorBrewerRcppRCurlreshape2restfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorsS7scalesSeqinfosnowSparseArraystringistringrSummarizedExperimentsysVariantAnnotationvctrsVGAMviridisLitewithrXMLXVectoryaml
