Description Usage Arguments Value Author(s) See Also Examples
Call and merge regions using joint posterior probabilities calculated by BAC.
1 | CallRegions(position,jointPP,cutoff=0.5,maxGap=500)
|
position |
A vector containing the probe genomic positions |
jointPP |
A vector containing the joint posterior probabilities as returned by BAC. |
cutoff |
The cutoff used to call regions. |
maxGap |
The maximum gap allowed between regions. Regions that are less than maxGap bps away will be merged. |
A vector containing the region index for each probe. Probes with the same positive index belong to the same region, whereas probe with index zero are background probes (not part of a bound region). These indices can be used to form a BED file, see example below.
Raphael Gottardo, raph@stat.ubc.ca
BAC
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 the data
data(ER)
# Only select the first 5000 probes for speed-up
ER<-ER[1:5000,]
# Calculate the joint posterior probabilities
#Only use 100 iterations for speed up (You should use more! See default value)
BAConER<-BAC(ER[,5:7], ER[,2:4], B=100,verbose=FALSE,w=5)
# For Regions using 0.5 cut-off for the joint posterior probabilities
ERregions<-CallRegions(ER[,1],BAConER$jointPP,cutoff=0.5,maxGap=500)
# Create the BED file
nRegions<-max(ERregions)
BED<-matrix(0,nRegions,4)
for(i in 1:nRegions)
{
BED[i,2:3]<-range(ER[ERregions==i,1])
#The score should be between 0 and 1000
BED[i,4]<-max(BAConER$jointPP[ERregions==i])*1000
}
BED<-data.frame(BED)
# The ER data is a subset of chr 21
BED[,1]<-"chr21"
names(BED)<-c("chrom","chromStart","chromEnd","Score")
# print it
print(BED)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.