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### =========================================================================
### Finding Somatic Mutations
### -------------------------------------------------------------------------
setGeneric("callSampleSpecificVariants", function(case, control, ...) {
standardGeneric("callSampleSpecificVariants")
})
### TODO: check for positions that are completely non-ref in normal
### and somehow gain the reference allele in tumor.
## NEW ALGORITHM
## - Filter out all normal calls from tumor calls
## - For the remaining tumor calls, ask two questions:
## - Did we have sufficient coverage in normal to make a call?
## - Is the normal frequency reasonable, given the tumor frequency?
## IDEAS FROM ROBERT:
## - Assume het frequency (~50%) for power and extremity filter.
## - But this will miss artifacts in the normal, and thus
## conclude that they are tumor-specific...
## - The power filter might work best as an annotation.
## - Maybe even assume het frequency when calling in normal,
## which would automatically fix the power filter.
## - Maybe discard tumor variants that look het, but risky;
## analysts always have access to frequencies.
setMethod("callSampleSpecificVariants", c("VRanges", "VRanges"),
function(case, control, control.cov, ...)
{
filters <- SampleSpecificVariantFilters(control,
control.cov,
hardFilters(case),
...)
case.specific <- subsetByFilter(case, filters)
annotateWithControlDepth(case.specific, control, control.cov)
})
setMethod("callSampleSpecificVariants", c("BamFile", "BamFile"),
function(case, control, tally.param,
calling.filters = VariantCallingFilters(),
post.filters = FilterRules(),
...)
{
case.raw <- tallyVariants(case, tally.param)
case.called <- callVariants(case.raw, calling.filters, post.filters)
control.raw <- tallyVariants(control, tally.param)
which <- tally.param@bamTallyParam@which
if (is(which, "GRangesList")) which<-unlist(which)
sbp <- ScanBamParam(which = which)
control.cov <- coverage(control, drop.D.ranges = TRUE, param = sbp)
callSampleSpecificVariants(case.called, control.raw,
control.cov=control.cov,
...)
})
setMethod("callSampleSpecificVariants", c("character", "character"),
function(case, control, ...)
{
callSampleSpecificVariants(BamFile(case), BamFile(control), ...)
})
SampleSpecificVariantFilters <-
function(control, control.cov, calling.filters, power = 0.8, p.value = 0.01)
{
control.called <- callVariants(control, calling.filters,
post.filters = FilterRules())
FilterRules(c(calledInControl = SetdiffVariantsFilter(control.called),
power = CallableInOtherFilter(control.cov, calling.filters,
power),
extremity = LowerFrequencyInOtherFilter(control, control.cov,
p.value)
))
}
SetdiffVariantsFilter <- function(other) {
function(x) {
!(x %in% other)
}
}
SetdiffPositionsFilter <- function(other) {
function(x) {
!(x %over% other)
}
}
extractCoverageForPositions <- function(cov, pos) {
if (length(setdiff(seqlevels(pos), names(cov))) > 0L)
stop("Some seqlevels are missing from coverage")
if (any(width(pos) > 1L))
stop("Some ranges are of width > 1")
seqlevels(pos) <- names(cov)
ord <- order(seqnames(pos))
ans <- integer(length(pos))
ans[ord] <- unlist(mapply(function(v, p) {
runValue(v)[findRun(p, v)]
}, cov, split(start(pos), seqnames(pos)), SIMPLIFY=FALSE), use.names=FALSE)
ans
}
CallableInOtherFilter <-
function(other.cov, calling.filters, min.power = 0.8,
p.lower = params(calling.filters$likelihoodRatio)$p.lower)
{
function(x) {
calculatePowerInOther(x, other.cov, calling.filters, p.lower) >= min.power
}
}
calculatePowerInOther <-
function(x, other.cov, calling.filters = hardFilters(x),
p.lower = params(calling.filters$likelihoodRatio)$p.lower)
{
lr.filter <- calling.filters$likelihoodRatio
if (is.null(lr.filter))
f <- 0
else
f <- lrtFreqCutoff(params(lr.filter)$p.error, params(lr.filter)$p.lower)
rc.filter <- calling.filters$readCount
if (is.null(rc.filter))
min.depth <- 0L
else
min.depth <- params(rc.filter)$min.depth
other.n <- extractCoverageForPositions(other.cov, resize(x, 1))
min.depth <- ceiling(pmax(min.depth, other.n * f))
1 - pbinom(min.depth-1L, other.n, p.lower)
}
LowerFrequencyInOtherFilter <- function(other, other.cov, p.value = 0.01)
{
function(x) {
## NOTE: this was once based on the raw (not quality filtered)
## counts, but bam_tally is no longer giving us those for the alts.
x <- annotateWithControlDepth(x, other, other.cov)
p <- with(x, pbinom(control.alt.depth, control.total.depth,
as.integer(altDepth / totalDepth)))
p < p.value
}
}
annotateWithControlDepth <- function(case, control, control.cov) {
m <- match(case, control)
control.alt.depth <- as.vector(altDepth(control))[m]
control.alt.depth[is.na(control.alt.depth)] <- 0L
control.total.depth <- as.vector(totalDepth(control))[m]
control.raw.total.depth <- as.vector(rawTotalDepth(control))[m]
control.raw.total.depth[is.na(m)] <-
extractCoverageForPositions(control.cov, resize(case[is.na(m)], 1))
control.total.depth[is.na(m)] <- control.raw.total.depth[is.na(m)]
case$control.alt.depth <- control.alt.depth
case$control.total.depth <- control.total.depth
case$control.raw.total.depth <- control.raw.total.depth
case
}
caseControlFET <- function(case, control, control.cov) {
case <- annotateWithControlDepth(case, control, control.cov)
with(case,
fisher_p(altDepth, (totalDepth - altDepth),
altDepth + control.alt.depth,
(totalDepth - altDepth) +
(control.total.depth - control.alt.depth)))
}
DepthFETFilter <- function(control, control.cov, p.value.cutoff = 0.05) {
function(x) {
p.value <- caseControlFET(x, control, control.cov)
p.value < p.value.cutoff
}
}
MaxControlFreqFilter <- function(control, control.cov, max.control.freq = 0.03) {
function(x) {
x <- annotateWithControlDepth(x, control, control.cov)
freq <- x$control.alt.depth / x$control.total.depth
ifelse(is.na(freq), 0, freq) <= max.control.freq
}
}
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