Description Usage Arguments Author(s) Examples
Create a junction track for IGV visualization of interection
1 2 3 4 5 6 7 8 9 10 | createIGVtrack(
pairs,
met.platform = "450K",
genome = "hg38",
filename = "ELMER_interactions.bed",
color.track = "black",
track.name = "junctions",
gene.symbol = NULL,
all.tss = TRUE
)
|
pairs |
A data frame output from getPairs function |
met.platform |
DNA methyaltion platform to retrieve data from: EPIC or 450K (default) |
genome |
Which genome build will be used: hg38 (default) or hg19. |
filename |
Filename (".bed") |
color.track |
A color for the track (i.e blue, red,#272E6A) |
track.name |
Track name |
gene.symbol |
Filter pairs to a single gene. |
all.tss |
A logical. If TRUE it will link probes to all TSS of a gene (transcript level), if FALSE it will link to the promoter region of a gene (gene level). |
Tiago Chedraoui Silva (tiagochst at gmail.com)
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 | ## Not run:
data <- ELMER:::getdata("elmer.data.example")
nearGenes <-GetNearGenes(TRange=getMet(data)[c("cg00329272","cg10097755"),],
geneAnnot=getExp(data))
Hypo.pair <- get.pair(data=data,
nearGenes=nearGenes,
permu.size=5,
group.col = "definition",
group1 = "Primary solid Tumor",
group2 = "Solid Tissue Normal",
raw.pvalue = 0.2,
Pe = 0.2,
dir.out="./",
label= "hypo")
createIGVtrack(Hypo.pair,met.platform = "450K", genome = "hg38")
## End(Not run)
|
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