View source: R/getBreakpoints.R
annotateBreakpoints | R Documentation |
Annotate breakpoints as sister-chromatid-exchange (SCE), copy-number-breakpoint (CNB).
annotateBreakpoints(breakpoints)
breakpoints |
A |
The input GRanges-class
with additinal column 'type'.
## Get an example BED file with single-cell-sequencing reads
bedfile <- system.file("extdata", "KK150311_VI_07.bam.bed.gz", package="AneuFinderData")
## Bin the data into bin size 1Mp
readfragments <- binReads(bedfile, assembly='mm10', binsize=1e6,
chromosomes=c(1:19,'X','Y'), reads.return=TRUE)
binned <- binReads(bedfile, assembly='mm10', binsize=1e6,
chromosomes=c(1:19,'X','Y'))
## Fit the Hidden Markov Model
model <- findCNVs.strandseq(binned[[1]])
## Add confidence intervals
breakpoints <- getBreakpoints(model, readfragments)
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