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## Fix as best as possible the bug in calculatePvalues() regarding the default | |
## maxRegionGap value. | |
## Usage: | |
# Step 1: open R in the main results folder | |
# Step 2: use fixChrs() with options of your choice | |
# fixChrs('chr') | |
## Alternatively use fixRegions() manually and re-run | |
## bumphunter::annotateNearest() | |
## Once all chrs have been fixed, re-run mergeResults() | |
library('derfinder') | |
fixRegions <- function(regions, fstats, models, coveragePrep, chr, | |
cutoffFstat = 1e-08, cutoffType = 'theoretical', | |
significantCut = c(0.05, 0.1), maxRegionGap = 0L, maxClusterGap = 300L, | |
lowMemDir = NULL) { | |
stopifnot(identical(names(regions), | |
c('regions', 'nullStats', 'nullWidths', 'nullPermutation'))) | |
cutoff <- derfinder:::.calcFstatCutoff(cutoffType, cutoffFstat, fstats, | |
models) | |
message(paste(Sys.time(), "F-stat cutoff to be used:", cutoff)) | |
new <- calculatePvalues(coveragePrep, models, fstats, nPermute = 0, | |
chr = chr, cutoff = cutoff, maxRegionGap = maxRegionGap, | |
maxClusterGap = maxClusterGap, lowMemDir = lowMemDir) | |
new$regions$pvalues <- derfinder:::.calcPval(new$regions$area, | |
as.numeric(regions$nullStats * regions$nullWidths)) | |
new$regions$significant <- factor(new$regions$pvalues < significantCut[1], | |
levels = c(TRUE, FALSE)) | |
qvalues <- qvalue::qvalue(new$regions$pvalues) | |
if (is(qvalues, "qvalue")) { | |
qvalues <- qvalues$qvalues | |
sigQval <- factor(qvalues < significantCut[2], levels = c(TRUE, | |
FALSE)) | |
} else { | |
message(paste(Sys.time(), "skipping q-value calculation.")) | |
qvalues <- rep(NA, length(regs$pvalues)) | |
sigQval <- rep(NA, length(regs$pvalues)) | |
} | |
new$regions$qvalues <- qvalues | |
new$regions$significantQval <- sigQval | |
new$nullStats <- regions$nullStats | |
new$nullWidths <- regions$nullWidths | |
new$nullPermutation <- regions$nullPermutation | |
new$note <- "Object fixed for bug in calculatePvalues(). Areas from null regions are approximated." | |
return(new) | |
} | |
fixChrs <- function(chr.pattern = 'chr', significantCut = c(0.05, 0.1), | |
maxRegionGap = 0L, maxClusterGap = 300L, subject = 'hg19', | |
runAnnotation = TRUE, lowMemDir = NULL) { | |
dirs <- dir(pattern = chr.pattern) | |
for(chr in dirs) { | |
message(paste(Sys.time(), 'fixing chromosome', chr)) | |
load(file.path(chr, 'coveragePrep.Rdata')) | |
load(file.path(chr, 'regions.Rdata')) | |
load(file.path(chr, 'fstats.Rdata')) | |
load(file.path(chr, 'optionsStats.Rdata')) | |
regions.original <- regions | |
## Save original regions for backup purposes | |
save(regions.original, file = file.path(chr, 'regions-original.Rdata')) | |
## Fix the regions. Note p-values will be approximated given that | |
## there is no way to truly fix the null areas without re-running | |
## derfinder | |
regions <- fixRegions(regions = regions.original, fstats = fstats, | |
models = optionsStats$models, coveragePrep = prep, | |
chr = chr, cutoffFstat = optionsStats$cutoffFstat, | |
cutoffType = optionsStats$cutoffType, | |
significantCut = significantCut, maxRegionGap = maxRegionGap, | |
maxClusterGap = maxClusterGap, lowMemDir = lowMemDir) | |
save(regions, file = file.path(chr, 'regions.Rdata')) | |
if(runAnnotation) { | |
load(file.path(chr, 'annotation.Rdata')) | |
annotation.original <- annotation | |
save(annotation.original, file = file.path(chr, | |
'annotation-original.Rdata')) | |
annotation <- bumphunter::annotateNearest(regions$regions, subject) | |
save(annotation, file = file.path(chr, 'annotation.Rdata')) | |
} | |
} | |
return(invisible(NULL)) | |
} |
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