org.Dm.egCHRLOC is an R object that maps entrez gene identifiers to the
starting position of the gene. The position of a gene is
measured as the number of base pairs.
The CHRLOCEND mapping is the same as the CHRLOC mapping except that it
specifies the ending base of a gene instead of the start.
Details
Each entrez gene identifier maps to a named vector of chromosomal locations,
where the name indicates the chromosome.
Chromosomal locations on both the sense and antisense strands are
measured as the number of base pairs from the p (5' end of the sense
strand) to q (3' end of the sense strand) arms. Chromosomal locations on the
antisense strand have a leading "-" sign (e. g. -1234567).
Since some genes have multiple start sites, this field can map to
multiple locations.
Mappings were based on data provided by: UCSC Genome Bioinformatics (Drosophila melanogaster)
ftp://hgdownload.cse.ucsc.edu/goldenPath/dm6
With a date stamp from the source of: 2014-Dec12
See Also
AnnotationDb-class for use of
the select() interface.
Examples
## select() interface:
## Objects in this package can be accessed using the select() interface
## from the AnnotationDbi package. See ?select for details.
## Bimap interface:
x <- org.Dm.egCHRLOC
# Get the entrez gene identifiers that are mapped to chromosome locations
mapped_genes <- mappedkeys(x)
# Convert to a list
xx <- as.list(x[mapped_genes])
if(length(xx) > 0) {
# Get the CHRLOC for the first five genes
xx[1:5]
# Get the first one
xx[[1]]
}
Results
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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> library(org.Dm.eg.db)
Loading required package: AnnotationDbi
Loading required package: stats4
Loading required package: BiocGenerics
Loading required package: parallel
Attaching package: 'BiocGenerics'
The following objects are masked from 'package:parallel':
clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
clusterExport, clusterMap, parApply, parCapply, parLapply,
parLapplyLB, parRapply, parSapply, parSapplyLB
The following objects are masked from 'package:stats':
IQR, mad, xtabs
The following objects are masked from 'package:base':
Filter, Find, Map, Position, Reduce, anyDuplicated, append,
as.data.frame, cbind, colnames, do.call, duplicated, eval, evalq,
get, grep, grepl, intersect, is.unsorted, lapply, lengths, mapply,
match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank,
rbind, rownames, sapply, setdiff, sort, table, tapply, union,
unique, unsplit
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")'.
Loading required package: IRanges
Loading required package: S4Vectors
Attaching package: 'S4Vectors'
The following objects are masked from 'package:base':
colMeans, colSums, expand.grid, rowMeans, rowSums
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/org.Dm.eg.db/org.Dm.egCHRLOC.Rd_%03d_medium.png", width=480, height=480)
> ### Name: org.Dm.egCHRLOC
> ### Title: Entrez Gene IDs to Chromosomal Location
> ### Aliases: org.Dm.egCHRLOC org.Dm.egCHRLOCEND
> ### Keywords: datasets
>
> ### ** Examples
>
> ## select() interface:
> ## Objects in this package can be accessed using the select() interface
> ## from the AnnotationDbi package. See ?select for details.
>
> ## Bimap interface:
> x <- org.Dm.egCHRLOC
> # Get the entrez gene identifiers that are mapped to chromosome locations
> mapped_genes <- mappedkeys(x)
> # Convert to a list
> xx <- as.list(x[mapped_genes])
> if(length(xx) > 0) {
+ # Get the CHRLOC for the first five genes
+ xx[1:5]
+ # Get the first one
+ xx[[1]]
+ }
3R 3R
7143486 7143728
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> dev.off()
null device
1
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