GenomicFeatures
|     | 
    
    This package is for version 3.2 of Bioconductor;
for the stable, up-to-date release version, see
GenomicFeatures.
    
    Tools for making and manipulating transcript centric annotations
    
        Bioconductor version: 3.2
    
    A set of tools and methods for making and manipulating transcript centric annotations. With these tools the user can easily download the genomic locations of the transcripts, exons and cds of a given organism, from either the UCSC Genome Browser or a BioMart database (more sources will be supported in the future). This information is then stored in a local database that keeps track of the relationship between transcripts, exons, cds and genes. Flexible methods are provided for extracting the desired features in a convenient format.
    Author: M. Carlson, H. Pagès, P. Aboyoun, S. Falcon, M. Morgan, D. Sarkar, M. Lawrence 
    Maintainer: Bioconductor Package Maintainer <maintainer at bioconductor.org> 
    
    Citation (from within R,
      enter citation("GenomicFeatures")):
      
     
    Installation
    To install this package, start R and enter:
    ## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("GenomicFeatures")
    Documentation
To view documentation for the version of this package installed
    in your system, start R and enter:
browseVignettes("GenomicFeatures")
     
    
        
        
        
            
                
                
                
                    | PDF |  | Making and Utilizing TxDb Objects | 
            
        
            
            
                | PDF |  | Reference Manual | 
            
            
                
                
                    | Text |  | NEWS | 
                
            
            
            
            
    
    Details
    
    
        
            | biocViews | Annotation, Genetics, GenomeAnnotation, Infrastructure, Sequencing, Software | 
        
            | Version | 1.22.13 | 
        
            
                | In Bioconductor since | BioC 2.5 (R-2.10) (6.5 years) | 
        
        
            | License | Artistic-2.0 | 
        
            | Depends | BiocGenerics(>= 0.1.0), S4Vectors(>= 0.7.17), IRanges(>= 2.3.21), GenomeInfoDb(>= 1.5.16), GenomicRanges(>= 1.21.32), AnnotationDbi(>= 1.27.9) | 
        
            | Imports | methods, utils, tools, DBI (>= 0.2-5), RSQLite (>= 0.8-1), RCurl, XVector, Biostrings(>= 2.23.3), rtracklayer(>= 1.29.24), biomaRt(>= 2.17.1), Biobase(>= 2.15.1) | 
        
            | LinkingTo |  | 
        
            | Suggests | org.Mm.eg.db, org.Hs.eg.db, BSgenome, BSgenome.Hsapiens.UCSC.hg19(>= 1.3.17), BSgenome.Celegans.UCSC.ce2, BSgenome.Dmelanogaster.UCSC.dm3(>= 1.3.17), mirbase.db, FDb.UCSC.tRNAs, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene(>= 2.7.1), TxDb.Mmusculus.UCSC.mm10.knownGene, TxDb.Hsapiens.UCSC.hg19.lincRNAsTranscripts, TxDb.Hsapiens.UCSC.hg38.knownGene, SNPlocs.Hsapiens.dbSNP141.GRCh38, Rsamtools, pasillaBamSubset(>= 0.0.5), GenomicAlignments, RUnit, BiocStyle, knitr | 
        
            | SystemRequirements |  | 
        
            | Enhances |  | 
        
            | URL |  | 
        
        
            | Depends On Me | cpvSNP, ensembldb, exomePeak, FDb.FANTOM4.promoters.hg19, FDb.InfiniumMethylation.hg18, FDb.InfiniumMethylation.hg19, FDb.UCSC.snp135common.hg19, FDb.UCSC.snp137common.hg19, FDb.UCSC.tRNAs, ggtut, Guitar, Homo.sapiens, InPAS, IVAS, Mus.musculus, mygene, OrganismDbi, Rattus.norvegicus, RNAprobR, SplicingGraphs, TxDb.Athaliana.BioMart.plantsmart22, TxDb.Athaliana.BioMart.plantsmart25, TxDb.Athaliana.BioMart.plantsmart28, TxDb.Celegans.UCSC.ce6.ensGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene, TxDb.Hsapiens.BioMart.igis, TxDb.Hsapiens.UCSC.hg18.knownGene, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Hsapiens.UCSC.hg19.lincRNAsTranscripts, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Mmusculus.UCSC.mm10.ensGene, TxDb.Mmusculus.UCSC.mm10.knownGene, TxDb.Mmusculus.UCSC.mm9.knownGene, TxDb.Rnorvegicus.BioMart.igis, TxDb.Rnorvegicus.UCSC.rn4.ensGene, TxDb.Rnorvegicus.UCSC.rn5.refGene, TxDb.Scerevisiae.UCSC.sacCer2.sgdGene, TxDb.Scerevisiae.UCSC.sacCer3.sgdGene | 
        
            | Imports Me | AllelicImbalance, AnnotationHubData, biovizBase, bumphunter, casper, ChIPpeakAnno, ChIPseeker, compEpiTools, CompGO, csaw, customProDB, derfinder, derfinderPlot, EDASeq, ELMER, EnsDb.Hsapiens.v75, EnsDb.Hsapiens.v79, EnsDb.Mmusculus.v75, EnsDb.Mmusculus.v79, EnsDb.Rnorvegicus.v75, EnsDb.Rnorvegicus.v79, epivizr, FDb.FANTOM4.promoters.hg19, FDb.InfiniumMethylation.hg18, FDb.InfiniumMethylation.hg19, FDb.UCSC.snp135common.hg19, FDb.UCSC.snp137common.hg19, FDb.UCSC.tRNAs, geneLenDataBase, ggbio, gmapR, gQTLstats, Gviz, gwascat, Homo.sapiens, HTSeqGenie, INSPEcT, lumi, metagene, methyAnalysis, Mus.musculus, PGA, proBAMr, qpgraph, QuasR, Rattus.norvegicus, rCGH, RiboProfiling, SGSeq, SplicingGraphs, systemPipeR, TCGAbiolinks, trackViewer, TxDb.Athaliana.BioMart.plantsmart22, TxDb.Athaliana.BioMart.plantsmart25, TxDb.Hsapiens.BioMart.igis, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Rnorvegicus.BioMart.igis, VariantAnnotation, VariantFiltering, VariantTools, wavClusteR | 
        
            | Suggests Me | AnnotationHub, biomvRCNS, Biostrings, BSgenome.Btaurus.UCSC.bosTau3, BSgenome.Btaurus.UCSC.bosTau4, BSgenome.Btaurus.UCSC.bosTau6, BSgenome.Btaurus.UCSC.bosTau8, BSgenome.Celegans.UCSC.ce10, BSgenome.Celegans.UCSC.ce11, BSgenome.Celegans.UCSC.ce2, BSgenome.Cfamiliaris.UCSC.canFam2, BSgenome.Cfamiliaris.UCSC.canFam3, BSgenome.Dmelanogaster.UCSC.dm2, BSgenome.Dmelanogaster.UCSC.dm6, BSgenome.Drerio.UCSC.danRer10, BSgenome.Drerio.UCSC.danRer5, BSgenome.Drerio.UCSC.danRer6, BSgenome.Drerio.UCSC.danRer7, BSgenome.Gaculeatus.UCSC.gasAcu1, BSgenome.Ggallus.UCSC.galGal3, BSgenome.Ggallus.UCSC.galGal4, BSgenome.Hsapiens.UCSC.hg17, BSgenome.Mmulatta.UCSC.rheMac2, BSgenome.Mmulatta.UCSC.rheMac3, BSgenome.Mmusculus.UCSC.mm8, BSgenome.Ptroglodytes.UCSC.panTro2, BSgenome.Ptroglodytes.UCSC.panTro3, BSgenome.Rnorvegicus.UCSC.rn6, chipseq, cummeRbund, DEXSeq, easyRNASeq, flipflop, GenomeInfoDb, GenomicAlignments, GenomicRanges, ggtut, groHMM, ind1KG, MiRaGE, parathyroidSE, RIPSeeker, Rsamtools, ShortRead, SummarizedExperiment | 
        
            
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