Makes a venn diagram for the regions given the genomic state showing how many regions overlap introns, exons, intergenic regions, none or multiple groups.
vennRegions(annotatedRegions, subsetIndex = NULL, ...)
The output from annotateRegions
used on regions
.
A vector of to use to subset the regions to use for the
venn diagram. It can be a logical vector of length equal to the number of
regions or an integer vector. If NULl
, then it's ignored.
Arguments passed to vennDiagram.
Makes a venn diagram plot for the annotation given the genomic state and the actual venn counts used to make the plot.
annotateRegions, vennCounts, vennDiagram
## Load data
library("derfinder")
## Annotate regions
annotatedRegions <- annotateRegions(
regions = genomeRegions$regions,
genomicState = genomicState$fullGenome, minoverlap = 1
)
#> 2024-12-12 22:19:21.535523 annotateRegions: counting
#> 2024-12-12 22:19:21.585362 annotateRegions: annotating
## Make venn diagram
venn <- vennRegions(annotatedRegions)
## Add title and choose text color
venn2 <- vennRegions(annotatedRegions,
main = "Venn diagram", counts.col =
"blue"
)
## Subset to only significant regions, so you don't have to annotate them
## again
venn3 <- vennRegions(annotatedRegions,
subsetIndex =
genomeRegions$regions$significant == "TRUE", main = "Significant only"
)