# NOT RUN {
## Simulate a sequence of Poisson data.
sim.seg <- function(seg.mean, size.mean=15){
seg.size <- rpois(1, size.mean)
rpois(seg.size, seg.mean)
}
set.seed(1)
seg.mean.vec <- c(1.5, 3.5, 0.5, 4.5, 2.5)
z.list <- lapply(seg.mean.vec, sim.seg)
z.rep.vec <- unlist(z.list)
## Plot the simulated data.
library(ggplot2)
count.df <- data.frame(
position=seq_along(z.rep.vec),
count=z.rep.vec)
gg.count <- ggplot()+
geom_point(aes(
position, count),
shape=1,
data=count.df)
gg.count
## Plot the true changepoints.
n.segs <- length(seg.mean.vec)
seg.size.vec <- sapply(z.list, length)
seg.end.vec <- cumsum(seg.size.vec)
change.vec <- seg.end.vec[-n.segs]+0.5
change.df <- data.frame(
changepoint=change.vec)
gg.change <- gg.count+
geom_vline(aes(
xintercept=changepoint),
data=change.df)
gg.change
## Fit a peak model and plot it.
fit <- PeakSegDisk::PeakSegFPOP_vec(z.rep.vec, 10.5)
gg.change+
geom_segment(aes(
chromStart+0.5, mean, xend=chromEnd+0.5, yend=mean),
color="green",
data=fit$segments)
## A pathological data set.
z.slow.vec <- 1:length(z.rep.vec)
fit.slow <- PeakSegDisk::PeakSegFPOP_vec(z.slow.vec, 10.5)
rbind(fit.slow$loss, fit$loss)
# }
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