Description Usage Arguments Value Examples
get annotation for genes and cytobands
1 2 3 4 5 6 | annoByGenesAndCyto(.Object, chr, beg, end, critical.genes, gene.uni.clean.gr,
cyto.gr)
## S4 method for signature 'Annotate'
annoByGenesAndCyto(.Object, chr, beg, end, critical.genes,
gene.uni.clean.gr, cyto.gr)
|
.Object |
the objet |
chr |
the chromosome |
beg |
genomic start coord |
end |
genomic end coord |
critical.genes |
set of critical genes |
gene.uni.clean.gr |
gr object of genes |
cyto.gr |
gr object of cyto positions |
list of annotation for genes and cytobands
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 | load(system.file("data", "allCall.lst.RData", package="BubbleTree"))
load(system.file("data", "cancer.genes.minus2.rda", package="BubbleTree"))
load(system.file("data", "vol.genes.rda", package="BubbleTree"))
load(system.file("data", "gene.uni.clean.gr.rda", package="BubbleTree"))
load(system.file("data", "cyto.gr.rda", package="BubbleTree"))
comm <- btcompare(vol.genes, cancer.genes.minus2)
btreeplotter <- new("BTreePlotter", branch.col="gray50")
annotator <-new("Annotate")
nn <- "sam2"
cc <- allCall.lst[[nn]]
z <- drawBTree(btreeplotter, cc@rbd.adj) +
ggplot2::labs(title=sprintf("%s (%s)", nn, info(cc)))
out <- cc@result$dist %>%
filter(seg.size >= 0.1 ) %>%
arrange(gtools::mixedorder(as.character(seqnames)), start)
ann <- annoByGenesAndCyto(annotator,
as.character(out$seqnames),
as.numeric(out$start),
as.numeric(out$end),
comm$comm,
gene.uni.clean.gr=gene.uni.clean.gr,
cyto.gr=cyto.gr)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.