Package: comapr 1.11.0
comapr: Crossover analysis and genetic map construction
comapr detects crossover intervals for single gametes from their haplotype states sequences and stores the crossovers in GRanges object. The genetic distances can then be calculated via the mapping functions using estimated crossover rates for maker intervals. Visualisation functions for plotting interval-based genetic map or cumulative genetic distances are implemented, which help reveal the variation of crossovers landscapes across the genome and across individuals.
Authors:
comapr_1.11.0.tar.gz
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comapr.pdf |comapr.html✨
comapr/json (API)
# Install 'comapr' in R: |
install.packages('comapr', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
- coCount - RangedSummarizedExperiment object containing the crossover counts across samples for the list of SNP marker intervals
- parents_geno - Parents' genotype for F1 samples in 'snp_geno'
- snp_geno - Markers by genotype results for a group of samples
- snp_geno_gr - Markers by genotype results for a group of samples
- twoSamples - RangedSummarizedExperiment object containing the Viterbi states SNP markers for samples from two groups. 'colData(twoSamples)' contains the sample group factor.
On BioConductor:comapr-1.9.0(bioc 3.20)comapr-1.8.0(bioc 3.19)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
softwaresinglecellvisualizationgenetics
Last updated 23 days agofrom:8257419c89. Checks:OK: 3 NOTE: 4. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Oct 30 2024 |
R-4.5-win | NOTE | Oct 30 2024 |
R-4.5-linux | NOTE | Oct 30 2024 |
R-4.4-win | NOTE | Oct 30 2024 |
R-4.4-mac | NOTE | Oct 31 2024 |
R-4.3-win | OK | Oct 30 2024 |
R-4.3-mac | OK | Oct 30 2024 |
Exports:bootstrapDistcalGeneticDistcombineHapStatecorrectGTcountBinStatecountCOscountGTfilterGTfindDupSamplesgetAFTracksgetCellAFTrackgetCellCORangegetCellDPTrackgetDistortedMarkersgetMeanDPTrackgetSNPDensityTrackperCellChrQCpermuteDistperSegChrQCplotCountplotGeneticDistplotGTFreqplotWholeGenomereadColMMreadHapState
Dependencies:abindAnnotationDbiAnnotationFilteraskpassbackportsbase64encBHBiobaseBiocFileCacheBiocGenericsBiocIOBiocParallelbiomaRtBiostringsbiovizBasebitbit64bitopsblobBSgenomebslibcachemcheckmatecirclizecliclustercodetoolscolorspacecpp11crayoncrosstalkcurldata.tableDBIdbplyrDelayedArraydeldirdichromatdigestdplyrensembldbevaluatefansifarverfastmapfilelockfontawesomeforeachforeignformatRFormulafsfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesggplot2GlobalOptionsgluegridExtragtableGvizhighrHmischmshtmlTablehtmltoolshtmlwidgetshttrhttr2interpIRangesisobanditeratorsjpegjquerylibjsonliteKEGGRESTknitrlabelinglambda.rlaterlatticelatticeExtralazyevallifecyclemagrittrMASSMatrixMatrixGenericsmatrixStatsmemoisemgcvmimemunsellnlmennetopensslpillarpkgconfigplogrplotlyplyrpngprettyunitsprogresspromisesProtGenericspurrrR6rappdirsRColorBrewerRcppRcppEigenRCurlreshape2restfulrRhtslibrjsonrlangrmarkdownrpartRsamtoolsRSQLiterstudioapirtracklayerS4ArraysS4VectorssassscalesshapesnowSparseArraystringistringrSummarizedExperimentsystibbletidyrtidyselecttinytexUCSC.utilsutf8VariantAnnotationvctrsviridisviridisLitewithrxfunXMLxml2XVectoryamlzlibbioc
Genetic distance calculation from genotype shifts of markers
Rendered fromgetStarted.Rmd
usingknitr::rmarkdown
on Oct 30 2024.Last update: 2021-12-31
Started: 2020-10-13
single-sperm-co-analysis
Rendered fromsingle-sperm-co-analysis.Rmd
usingknitr::rmarkdown
on Oct 30 2024.Last update: 2021-09-26
Started: 2021-01-21
Readme and manuals
Help Manual
Help page | Topics |
---|---|
bootstrapDist | bootstrapDist |
calGeneticDist | calGeneticDist calGeneticDist,GRanges,missing,ANY,ANY,character-method calGeneticDist,GRanges,missing,ANY,ANY,missing-method calGeneticDist,GRanges,numeric,ANY,ANY,character-method calGeneticDist,GRanges,numeric,ANY,ANY,missing-method calGeneticDist,RangedSummarizedExperiment,missing,ANY,ANY,character-method calGeneticDist,RangedSummarizedExperiment,missing,ANY,ANY,missing-method calGeneticDist,RangedSummarizedExperiment,numeric,ANY,ANY,character-method calGeneticDist,RangedSummarizedExperiment,numeric,ANY,ANY,missing-method |
RangedSummarizedExperiment object containing the crossover counts across samples for the list of SNP marker intervals | coCount |
'comapr' package | comapr |
combineHapState | combineHapState |
correctGT | correctGT |
countBinState | countBinState |
countCOs | countCOs countCOs,GRanges-method countCOs,RangedSummarizedExperiment-method |
countGT | countGT |
filterGT | filterGT filterGT,GRanges,numeric,numeric-method filterGT,matrix,numeric,numeric-method |
findDupSamples | findDupSamples |
getAFTracks | getAFTracks |
getCellAFTrack Generates the DataTracks for plotting AF and crossover regions | getCellAFTrack |
getCellCORange | getCellCORange |
getCellDPTrack Generates the DataTrack for plotting DP of a selected cell | getCellDPTrack |
getDistortedMarkers | getDistortedMarkers |
getMeanDPTrack | getMeanDPTrack |
getSNPDensityTrack | getSNPDensityTrack |
Parents' genotype for F1 samples in `snp_geno` | parents_geno |
perCellChrQC | perCellChrQC |
permuteDist | permuteDist |
perSegChrQC | perSegChrQC |
plotCount | plotCount plotCount,GRanges,logical,character-method plotCount,GRanges,logical,missing-method plotCount,GRanges,missing,character-method plotCount,GRanges,missing,missing-method plotCount,RangedSummarizedExperiment,logical,character-method plotCount,RangedSummarizedExperiment,logical,missing-method plotCount,RangedSummarizedExperiment,missing,character-method plotCount,RangedSummarizedExperiment,missing,missing-method |
plotGeneticDist | plotGeneticDist |
plotGTFreq | plotGTFreq |
Plot cumulative genetic distances across the genome | plotWholeGenome |
readColMM | readColMM |
readHapState | readHapState |
Markers by genotype results for a group of samples | snp_geno |
Markers by genotype results for a group of samples | snp_geno_gr |
RangedSummarizedExperiment object containing the Viterbi states SNP markers for samples from two groups. `colData(twoSamples)` contains the sample group factor. | twoSamples |