Nothing
library(chipseq)
load("pairedReads.rda")
summarizeLane <- function(clist, summary.fun, ..., seqlen)
{
## clist is a list at the lane level, with one list("+"=, "-"=) for each chromsome
stopifnot(all(names(clist) %in% names(seqlen)))
seqlen <- seqlen[names(clist)]
mapply(summary.fun, clist, seqlen, ..., SIMPLIFY = FALSE)
}
summarizeReads <-
function(reads.list, lanes = c("1", "2", "3", "4", "6", "7", "8"), ...,
verbose = TRUE)
{
if (verbose) cat(paste("Processing lanes", paste(lanes, collapse = ",")), fill = TRUE)
lapply(reads.list[lanes], summarizeLane, ...)
}
coverageSummary <-
function(x, max = max(end(g)) + 400L)
## x is a list at the lane->chromosome level, with components "+" and "-"
{
g <- extendReads(x)
coverage(g, width = max)
}
## paired end reads
## lane1: mouse fibroblasts expressing Myod, 3 antibodies combined
## lane2: C2C12 myotube, 3 antibodies combined
## lane3: human fibroblast expressing Myod, antibody 7311
## lane4: human fibroblast expressing Myod, antibody 6975b
## lane6: human fibroblast expressing Myod, antibody 6196
## lane7: human fibroblast controls, 3 antibodies combined
## lane8: human fibroblast expressing Myod, 3 antibodies combined
library("BSgenome.Hsapiens.UCSC.hg18")
human.seqlens <- seqlengths(Hsapiens)
pairedEndHumanCoverage <-
summarizeReads(pairedReads,
lanes = c("3", "4", "6", "7", "8"),
summary.fun = coverageSummary,
seqlen = human.seqlens)
save(pairedEndHumanCoverage, file = "pairedEndHumanCoverage.rda")
isldf <-
do.call(make.groups,
lapply(pairedEndHumanCoverage,
function(x) viewMaxs(slice(x[["chr2"]], lower = 1))))
dotplot(xtabs(~data + which, isldf),
horizontal = FALSE, groups = FALSE,
scales = list(y = list(log = 2), x = list(rot = 90)),
aspect = "xy")
dotplot(xtabs(~data + which, isldf),
horizontal = FALSE, type = "o",
par.settings = simpleTheme(pch = 16),
auto.key = list(columns = 5),
aspect = "xy",
scales = list(y = list(log = 2), x = list(rot = 90)))
## conclusion: 10 seems to be a good coverage cutoff
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