Package: VariantAnnotation 1.51.0

Bioconductor Package Maintainer

VariantAnnotation: Annotation of Genetic Variants

Annotate variants, compute amino acid coding changes, predict coding outcomes.

Authors:Valerie Oberchain [aut], Martin Morgan [aut], Michael Lawrence [aut], Stephanie Gogarten [ctb], Bioconductor Package Maintainer [cre]

VariantAnnotation_1.51.0.tar.gz
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VariantAnnotation_1.51.0.tar.gz(r-4.5-noble)VariantAnnotation_1.51.0.tar.gz(r-4.4-noble)
VariantAnnotation.pdf |VariantAnnotation.html
VariantAnnotation/json (API)
NEWS

# Install 'VariantAnnotation' in R:
install.packages('VariantAnnotation', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org'))

Peer review:

Uses libs:
  • curl– Easy-to-use client-side URL transfer library
  • bzip2– High-quality block-sorting file compressor library
  • xz-utils– XZ-format compression library
  • zlib– Compression library

On BioConductor:VariantAnnotation-1.51.0(bioc 3.20)VariantAnnotation-1.50.0(bioc 3.19)

This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.

bioconductor-package

126 exports 7.20 score 69 dependencies 152 dependents 47 mentions

Last updated 2 months agofrom:6d549f2c16

Exports:AllVariantsaltalt<-altDepthaltDepth<-altFractionasVCFcalledcbindCodingVariantscolumnsdownstreamdownstream<-duplicateRSIDexpandfiltfilt<-filterVcfFiveUTRVariantsfixedfixed<-genogeno<-genomegenotypeCodesToNucleotidesgenotypeToSnpMatrixgetSeqgetTranscriptSeqsGLtoGPhardFiltershardFilters<-headerheader<-idTypeidType<-importindexVcfinfoinfo<-intergenicintergenic<-IntergenicVariantsIntronVariantsisDeletionisDelinsisIndelisInsertionisSNVisSubstitutionisTransitionkeyskeytypeslocateVariantsmakeVRangesFromGRangesmcols<-metameta<-PLtoGPpost_Hs_regionpredictCodingprobabilityToSnpMatrixpromoterpromoter<-PromoterVariantsqualqual<-rbindreadGenoreadGTreadInforeadVcfreadVcfAsVRangesrefref<-refDepthrefDepth<-referenceresetFiltersampleNamessampleNames<-samplesscanVcfscanVcfHeaderScanVcfParamselectseqinfoseqlevelssnpSummarysoftFiltersoftFilterMatrixsoftFilterMatrix<-SpliceSiteVariantsstackSamplesstrandstrand<-subsetsummarizeVariantstabulateThreeUTRVariantstotalDepthtotalDepth<-updateObjectupstreamupstream<-VCFvcfFieldsVcfFileVcfFileListvcfFixedvcfFixed<-vcfGenovcfGeno<-VCFHeadervcfInfovcfInfo<-vcfSamplesvcfSamples<-vcfTrimEmptyvcfTrimEmpty<-vcfWhichvcfWhich<-vep_by_regionVRangesVRangesListVRangesScanVcfParamwriteVcf

Dependencies:abindAnnotationDbiaskpassBHBiobaseBiocGenericsBiocIOBiocParallelBiostringsbitbit64bitopsblobBSgenomecachemclicodetoolscpp11crayoncurlDBIDelayedArrayfastmapformatRfutile.loggerfutile.optionsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesgluehttrIRangesjsonliteKEGGRESTlambda.rlatticelifecycleMatrixMatrixGenericsmatrixStatsmemoisemimeopensslpkgconfigplogrpngR6RCurlrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorssnowSparseArraySummarizedExperimentsysUCSC.utilsvctrsXMLXVectoryamlzlibbioc

Introduction to VariantAnnotation

Rendered fromVariantAnnotation.Rmdusingknitr::rmarkdownon Jun 30 2024.

Last update: 2023-06-02
Started: 2023-06-02

Using filterVcf() to Select Variants from VCF Files

Rendered fromfilterVcf.Rmdusingknitr::rmarkdownon Jun 30 2024.

Last update: 2023-06-02
Started: 2023-06-02

ensemblVEP: using the REST API with Bioconductor

Rendered fromensemblVEP.Rmdusingknitr::rmarkdownon Jun 30 2024.

Last update: 2024-01-26
Started: 2024-01-26

Readme and manuals

Help Manual

Help pageTopics
Filter VCF filesfilterVcf filterVcf,character-method filterVcf,TabixFile-method
Convert genotype calls from a VCF file to a SnpMatrix objectgenotypeToSnpMatrix genotypeToSnpMatrix,array-method genotypeToSnpMatrix,CollapsedVCF-method
Get transcript sequencesgetTranscriptSeqs getTranscriptSeqs,GRanges,FaFile-method getTranscriptSeqs,GRangesList,ANY-method getTranscriptSeqs,GRangesList,BSgenome-method getTranscriptSeqs,GRangesList,FaFile-method
Convert genotype likelihoods to genotype probabilitiesGLtoGP PLtoGP
Create index files for VCF filesindexVcf indexVcf,character-method indexVcf,VcfFile-method indexVcf,VcfFileList-method
Identification of genomic variant types.isDeletion isDeletion,CollapsedVCF-method isDeletion,ExpandedVCF-method isDeletion,VRanges-method isDelins isDelins,CollapsedVCF-method isDelins,ExpandedVCF-method isDelins,VRanges-method isIndel isIndel,CollapsedVCF-method isIndel,ExpandedVCF-method isIndel,VRanges-method isInsertion isInsertion,CollapsedVCF-method isInsertion,ExpandedVCF-method isInsertion,VRanges-method isSNV isSNV,CollapsedVCF-method isSNV,ExpandedVCF-method isSNV,VRanges-method isSubstitution isSubstitution,CollapsedVCF-method isSubstitution,ExpandedVCF-method isSubstitution,VRanges-method isTransition isTransition,CollapsedVCF-method isTransition,ExpandedVCF-method isTransition,VRanges-method
Locate variantslocateVariants locateVariants,GRanges,GRangesList,AllVariants-method locateVariants,GRanges,GRangesList,CodingVariants-method locateVariants,GRanges,GRangesList,FiveUTRVariants-method locateVariants,GRanges,GRangesList,IntergenicVariants-method locateVariants,GRanges,GRangesList,IntronVariants-method locateVariants,GRanges,GRangesList,PromoterVariants-method locateVariants,GRanges,GRangesList,SpliceSiteVariants-method locateVariants,GRanges,GRangesList,ThreeUTRVariants-method locateVariants,GRanges,GRangesList,VariantType-method locateVariants,GRanges,TxDb,AllVariants-method locateVariants,GRanges,TxDb,CodingVariants-method locateVariants,GRanges,TxDb,FiveUTRVariants-method locateVariants,GRanges,TxDb,IntergenicVariants-method locateVariants,GRanges,TxDb,IntronVariants-method locateVariants,GRanges,TxDb,PromoterVariants-method locateVariants,GRanges,TxDb,SpliceSiteVariants-method locateVariants,GRanges,TxDb,ThreeUTRVariants-method locateVariants,GRanges,TxDb,VariantType-method locateVariants,IntegerRanges,GRangesList,VariantType-method locateVariants,IntegerRanges,TxDb,VariantType-method locateVariants,VCF,GRangesList,VariantType-method locateVariants,VCF,TxDb,VariantType-method
PolyPhenDb objectsclass:PolyPhenDb columns,PolyPhenDb-method duplicateRSID keys,PolyPhenDb-method metadata,PolyPhenDb-method PolyPhen PolyPhenDb PolyPhenDb-class select,PolyPhenDb-method
PolyPhenDb ColumnsPolyPhenDbColumns
elementary vep/homo_sapiens/region call to ensembl VEP REST APIpost_Hs_region
Predict amino acid coding changes for variantspredictCoding predictCoding,CollapsedVCF,TxDb,ANY,missing-method predictCoding,ExpandedVCF,TxDb,ANY,missing-method predictCoding,GRanges,TxDb,ANY,DNAStringSet-method predictCoding,IntegerRanges,TxDb,ANY,DNAStringSet-method predictCoding,VRanges,TxDb,ANY,missing-method
Convert posterior genotype probability to a SnpMatrix objectprobabilityToSnpMatrix
PROVEANDb objectsclass:PROVEANDb columns,PROVEANDb-method keys,PROVEANDb-method keytypes,PROVEANDb-method PROVEAN PROVEANDb PROVEANDb-class select,PROVEANDb-method
Read VCF filesimport,VcfFile,ANY,ANY-method readGeno readGT readInfo readVcf readVcf,character,ANY-method readVcf,character,missing-method readVcf,TabixFile,GRanges-method readVcf,TabixFile,GRangesList-method readVcf,TabixFile,IntegerRangesList-method readVcf,TabixFile,missing-method readVcf,TabixFile,ScanVcfParam-method
Import VCF filesscanVcf scanVcf,character,missing-method scanVcf,character,ScanVcfParam-method scanVcf,connection,missing-method scanVcf,TabixFile,GRanges-method scanVcf,TabixFile,IntegerRangesList-method scanVcf,TabixFile,missing-method scanVcf,TabixFile,ScanVcfParam-method scanVcfHeader scanVcfHeader,character-method scanVcfHeader,missing-method scanVcfHeader,TabixFile-method
Parameters for scanning VCF filesScanVcfParam ScanVcfParam,ANY-method ScanVcfParam,missing-method ScanVcfParam-class vcfFixed vcfFixed<- vcfGeno vcfGeno<- vcfInfo vcfInfo<- vcfSamples vcfSamples<- vcfTrimEmpty vcfTrimEmpty<- vcfWhich vcfWhich<-
Get seqinfo for VCF fileseqinfo seqinfo,VcfFile-method seqinfo,VcfFileList-method
SIFTDb objectsclass:SIFTDb columns,SIFTDb-method keys,SIFTDb-method metadata,SIFTDb-method select,SIFTDb-method SIFT SIFTDb SIFTDb-class
SIFTDb ColumnsSIFTDbColumns
Counts and distribution statistics for SNPs in a VCF objectsnpSummary snpSummary,CollapsedVCF-method
Summarize variants by samplesummarizeVariants summarizeVariants,GRangesList,VCF,function-method summarizeVariants,GRangesList,VCF,VariantType-method summarizeVariants,TxDb,VCF,CodingVariants-method summarizeVariants,TxDb,VCF,FiveUTRVariants-method summarizeVariants,TxDb,VCF,IntronVariants-method summarizeVariants,TxDb,VCF,PromoterVariants-method summarizeVariants,TxDb,VCF,SpliceSiteVariants-method summarizeVariants,TxDb,VCF,ThreeUTRVariants-method
helper function to construct inputs for VEP REST APIvariant_body
Defunct Functions in Package 'VariantAnnotation'dbSNPFilter MatrixToSnpMatrix readVcfLongForm readVcfLongForm,character,character,missing-method readVcfLongForm,character,character,ScanVcfParam-method readVcfLongForm,character,missing,missing-method readVcfLongForm,TabixFile,character,GRanges-method readVcfLongForm,TabixFile,character,IntegerRangesList-method readVcfLongForm,TabixFile,character,missing-method readVcfLongForm,TabixFile,character,ScanVcfParam-method refLocsToLocalLocs refLocsToLocalLocs,GRanges,missing,GRangesList-method refLocsToLocalLocs,GRanges,TxDb,missing-method regionFilter restrictToSNV VariantAnnotation-defunct VRangesScanVcfParam
VariantType subclassesAllVariants AllVariants-class CodingVariants CodingVariants-class downstream downstream,AllVariants-method downstream,IntergenicVariants-method downstream,PromoterVariants-method downstream<- downstream<-,AllVariants-method downstream<-,IntergenicVariants-method downstream<-,PromoterVariants-method FiveUTRVariants FiveUTRVariants-class idType idType,IntergenicVariants-method idType<- idType<-,IntergenicVariants-method intergenic intergenic,AllVariants-method intergenic<- intergenic<-,AllVariants-method IntergenicVariants IntergenicVariants-class IntronVariants IntronVariants-class promoter promoter,AllVariants-method promoter<- promoter<-,AllVariants-method PromoterVariants PromoterVariants-class show,AllVariants-method show,PromoterVariants-method show,VariantType-method SpliceSiteVariants SpliceSiteVariants-class ThreeUTRVariants ThreeUTRVariants-class upstream upstream,AllVariants-method upstream,IntergenicVariants-method upstream,PromoterVariants-method upstream<- upstream<-,AllVariants-method upstream<-,IntergenicVariants-method upstream<-,PromoterVariants-method VariantType-class
VCF class objectsalt alt,VCF-method alt<- alt<-,CollapsedVCF,CharacterList-method alt<-,CollapsedVCF,DNAStringSetList-method alt<-,ExpandedVCF,character-method alt<-,ExpandedVCF,DNAStringSet-method cbind,VCF-method class:CollapsedVCF class:ExpandedVCF class:VCF CollapsedVCF CollapsedVCF-class dimnames<-,VCF,list-method expand,CollapsedVCF-method expand,ExpandedVCF-method ExpandedVCF ExpandedVCF-class filt filt,VCF-method filt<- filt<-,VCF,character-method fixed fixed,VCF-method fixed<- fixed<-,VCF,DataFrame-method geno geno,VCF,ANY-method geno,VCF,character-method geno,VCF,numeric-method geno,VCF-method geno,VCFHeader,ANY-method geno<- geno<-,VCF,character,matrix-method geno<-,VCF,missing,matrix-method geno<-,VCF,missing,SimpleList-method geno<-,VCF,numeric,matrix-method genome,VCF-method genotypeCodesToNucleotides header,VCF-method header<- header<-,VCF,VCFHeader-method info info,VCF-method info<- info<-,VCF,DataFrame-method mcols<-,VCF,ANY-method mcols<-,VCF-method qual qual,VCF-method qual<- qual<-,VCF,numeric-method rbind,VCF-method ref ref,VCF-method ref<- ref<-,VCF,DNAStringSet-method rowRanges,VCF-method rowRanges<-,VCF,GRanges-method seqlevels,VCF-method show,CollapsedVCF-method show,ExpandedVCF-method show,VCF-method SnpMatrixToVCF strand,VCF-method strand<-,VCF,ANY-method subset,VCF-method updateObject,VCF-method VCF VCF-class vcfFields,VCF-method [,VCF,ANY,ANY,ANY-method [,VCF,ANY,ANY-method [,VCF-method [<-,VCF,ANY,ANY,VCF-method
Manipulate Variant Call Format (Vcf) files.vcfFields,character-method vcfFields,missing-method vcfFields,VcfFile-method vcfFields,VcfFileList-method VcfFile VcfFile-class VcfFileList VcfFileList-class
VCFHeader instancescontig contig,VCFHeader-method fixed,VCFHeader-method fixed<-,VCFHeader,DataFrameList-method geno,VCFHeader-method geno<-,VCFHeader,missing,DataFrame-method header header,VCFHeader-method info,VCFHeader-method info<-,VCFHeader,DataFrame-method meta meta,VCFHeader-method meta<- meta<-,VCFHeader,DataFrame-method meta<-,VCFHeader,DataFrameList-method reference reference,VCFHeader-method samples samples,VCFHeader-method seqinfo,VCFHeader-method show,VCFHeader-method vcfFields vcfFields,VCFHeader-method VCFHeader VCFHeader-class
Use the VEP region API on variant information in a VCF object as defined in VariantAnnotation.vep_by_region
VRanges objectsalt,VRanges-method alt<-,VRanges,ANY-method altDepth altDepth,VRanges-method altDepth<- altDepth<-,VRanges-method altFraction altFraction,VRanges-method asVCF asVCF,VRanges-method called called,VRanges-method characterOrRle-class characterRle-class class:VRanges coerce,GRanges,VRanges-method coerce,VCF,VRanges-method coerce,VRanges,VCF-method complexRle-class factorOrRle-class factorRle-class hardFilters hardFilters,VRanges-method hardFilters<- hardFilters<-,VRanges-method integerOrRle-class integerRle-class logicalRle-class makeVRangesFromGRanges match,VRanges,VRanges-method numericRle-class rawRle-class readVcfAsVRanges ref,VRanges-method ref<-,VRanges,ANY-method refDepth refDepth,VRanges-method refDepth<- refDepth<-,VRanges-method resetFilter sampleNames,VRanges-method sampleNames<-,VRanges,ANY-method softFilter softFilterMatrix softFilterMatrix,VRanges-method softFilterMatrix<- softFilterMatrix<-,VRanges-method tabulate tabulate,VRanges-method totalDepth totalDepth,VRanges-method totalDepth<- totalDepth<-,VRanges-method VRanges VRanges-class writeVcf,VRanges,ANY-method
VRangesList objectsalt,VRangesList-method class:CompressedVRangesList class:SimpleVRangesList class:VRangesList CompressedVRangesList-class ref,VRangesList-method SimpleVRangesList-class stackSamples stackSamples,VRangesList-method VRangesList VRangesList-class
Write VCF fileswriteVcf writeVcf,VCF,character-method writeVcf,VCF,connection-method