Generate annotation features (feature.gr for view3dStructure) from TxDb and Org object.
getFeatureGR(
txdb,
org,
range,
keytype = "ENTREZID",
geneSymbolColumn = "SYMBOL",
cols = seq.int(7)
)A GRanges object
library(TxDb.Hsapiens.UCSC.hg38.knownGene)
#> Loading required package: GenomicFeatures
#> Loading required package: BiocGenerics
#> Loading required package: generics
#>
#> Attaching package: 'generics'
#> The following objects are masked from 'package:base':
#>
#> as.difftime, as.factor, as.ordered, intersect, is.element, setdiff,
#> setequal, union
#>
#> Attaching package: 'BiocGenerics'
#> The following objects are masked from 'package:stats':
#>
#> IQR, mad, sd, var, xtabs
#> The following objects are masked from 'package:base':
#>
#> Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append,
#> as.data.frame, basename, cbind, colnames, dirname, do.call,
#> duplicated, eval, evalq, get, grep, grepl, is.unsorted, lapply,
#> mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int,
#> rank, rbind, rownames, sapply, saveRDS, table, tapply, unique,
#> unsplit, which.max, which.min
#> Loading required package: S4Vectors
#> Loading required package: stats4
#>
#> Attaching package: 'S4Vectors'
#> The following object is masked from 'package:utils':
#>
#> findMatches
#> The following objects are masked from 'package:base':
#>
#> I, expand.grid, unname
#> Loading required package: IRanges
#> Loading required package: Seqinfo
#> Loading required package: GenomicRanges
#> Loading required package: AnnotationDbi
#> Loading required package: Biobase
#> Welcome to Bioconductor
#>
#> Vignettes contain introductory material; view with
#> 'browseVignettes()'. To cite Bioconductor, see
#> 'citation("Biobase")', and for packages 'citation("pkgname")'.
library(org.Hs.eg.db)
#>
library(GenomicRanges)
range <- GRanges("chr21:28000001-29200000")
feature.gr <- getFeatureGR(txdb = TxDb.Hsapiens.UCSC.hg38.knownGene,
org = org.Hs.eg.db,
range = range)
#> 2169 genes were dropped because they have exons located on both strands of
#> the same reference sequence or on more than one reference sequence, so cannot
#> be represented by a single genomic range.
#> Use 'single.strand.genes.only=FALSE' to get all the genes in a GRangesList
#> object, or use suppressMessages() to suppress this message.
#> 'select()' returned 1:1 mapping between keys and columns