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coMET (version 1.4.4)

COSMIC_UCSC: Create one track of the genomic positions of variants from COSMIC

Description

Create one track of the genomic positions of variants from COSMIC, the "Catalogue Of Somatic Mutations In Cancer" using the Gviz bioconductor package

Usage

COSMIC_UCSC(gen, chr, start, end, showId=FALSE)

Arguments

gen
the name of the genome. Data is not currently available for GRCh38 (hg38)
chr
the chromosome of interest
start
the first position in the region of interest (the smallest value)
end
the last position in the region of interest (the largest value)
showId
Show the ID of the genetic elements

Value

An UcscTrack object of Gviz

References

http://bioconductor.org/packages/release/bioc/html/Gviz.html

http://genome-euro.ucsc.edu/cgi-bin/hgTrackUi?hgsid=202839739_2hYQ1BAOuBMAR620GjrtdrFAy6dn&c=chr6&g=cosmic

See Also

snpLocations_UCSC, structureBiomart_ENSEMBL, snpBiomart_ENSEMBL, CoreillCNV_UCSC, ClinVarMain_UCSC, ClinVarCnv_UCSC,

Examples

Run this code
library("Gviz")
chrom <- "chr2"
start <- 38290160
end <- 38303219
gen <- "hg19"
if(interactive()){
    cosmicVariant<-COSMIC_UCSC(gen,chrom,start,end)
    plotTracks(cosmicVariant, from = start, to =end)
}else {
    data(cosmicVarianttrack)
    plotTracks(cosmicVariant, from = start, to =end)
}

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