View source: R/BiofeatureGraphics.R
ISCA_UCSC | R Documentation |
Create one track of the genomic positions of variants from International Standards for Cytogenomic Arrays (ISCA) Consortium using the Gviz bioconductor package (obselete datbase, Impossible to access to data from UCSC from September 2015)
ISCA_UCSC(gen, chr, start, end, mySession, table.name,title="ISCA", showId=FALSE)
gen |
the name of the genome |
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) |
mySession |
the object session from the function browserSession of rtracklayer |
table.name |
A table of ISCAT classifications: iscaBenign, iscaCuratedBenign, iscaCuratedPathogenic, iscaLikelyBenign, iscaLikelyPathogenic, iscaPathGainCum, iscaPathLossCum, iscaPathogenic, iscaUncertain |
title |
The name of the annotation track |
showId |
Show the ID of the genetic elements |
An UcscTrack object of Gviz
Tiphaine Martin
http://genome-euro.ucsc.edu/cgi-bin/hgTrackUi?hgsid=202839739_2hYQ1BAOuBMAR620GjrtdrFAy6dn&c=chr6&g=iscaComposite
http://bioconductor.org/packages/release/bioc/html/Gviz.html
GWAScatalog_UCSC
, knownGenes_UCSC
, genesName_ENSEMBL
,
GeneReviews_UCSC
, GAD_UCSC
, genes_ENSEMBL
, xenorefGenes_UCSC
, transcript_ENSEMBL
,
# Oboselet function library("Gviz") library("rtracklayer") gen <- "hg19" chr <- "chr2" start <- 38292433 end <- 38305492 if(interactive()){ BROWSER.SESSION="UCSC" mySession <- browserSession(BROWSER.SESSION) genome(mySession) <- gen iscatrack <-ISCA_UCSC(gen,chrom,start,end,mySession,title="ISCA", table="iscaPathogenic") plotTracks(iscatrack, from = start, to =end, fontfamily="sans",fontfamily.title="sans") } else { data(ISCAtrack_Grch38) plotTracks(iscatrack, from = start, to =end, fontfamily="sans",fontfamily.title="sans") }
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