Nothing
# vcf=ExpandedVCF ----
setMethod(
"addOverallFrequencies", c("ExpandedVCF"),
function(vcf, force = FALSE){
.addOverallFrequencies(vcf, force)
}
)
# Main method ----
# vcf = ExpandedVCF
# force = logical(1)
.checkOverallInfo <- function(vcf, force){
stopifnot("TVTBparam" %in% names(metadata(vcf)))
param <- metadata(vcf)[["TVTBparam"]]
validObject(param@genos)
infoKeys <- suffix(param)
matchesHeader <- na.omit(match(infoKeys, rownames(info(header(vcf)))))
matchesData <- na.omit(match(infoKeys, colnames(info(vcf))))
# Process data first to avoid VCF validity warning
if ((length(matchesData) > 0)){
if (force){
# Remove fields from data
message(
"Overwriting INFO keys in data:\n- ",
paste(colnames(info(vcf))[matchesData], collapse = "\n- ")
)
info(vcf) <- info(vcf)[,-matchesData, drop = FALSE]
} else{
stop(
"INFO keys already present in data: ",
paste(colnames(info(vcf))[matchesData], collapse = "\n- ")
)
}
}
# Process header last to avoid VCF validity warning
if ((length(matchesHeader) > 0)){
if (force){
# Remove fields from header
message(
"Overwriting INFO keys in header:\n- ",
paste(
rownames(info(header(vcf)))[matchesHeader],
collapse = "\n- "
)
)
info(header(vcf)) <- info(header(vcf))[-matchesHeader,]
} else{
stop(
"INFO keys already present in header:\n- ",
paste(
rownames(info(header(vcf)))[matchesHeader],
collapse = "\n- ")
)
}
}
# Return vcf, trimmed if necessary
return(vcf)
}
# vcf = ExpandedVCF
# force = logical(1)
.addOverallFrequencies <- function(vcf, force){
# Check presence of required INFO keys: drop or throw error
vcf <- .checkOverallInfo(vcf, force)
# Shortcut
GT <- geno(vcf)[["GT"]]
param <- metadata(vcf)[["TVTBparam"]]
# TODO: could launch 3 parallel threads to count genotypes
# Count of REF, HET, ALT genotypes
REF <- .countGenos(GT, ref(param))
HET <- .countGenos(GT, het(param))
ALT <- .countGenos(GT, alt(param))
# Alternate allele frequency
AAF <- (HET + 2 * ALT) / (2 * (REF + HET + ALT))
# Minor allele frequency
MAF <- bpmapply(
function(ref, alt){min(ref, alt)},
ref = 1 - AAF,
alt = AAF,
BPPARAM = bp(param)
)
# Collate new headers
newInfoHeader <- DataFrame(
Number = rep(1, 5),
Type = c(rep("Integer", 3), rep("Float", 2)),
Description = c(
"Number of homozygote reference genotypes",
"Number of heterozygous genotypes",
"Number of homozygote alternate genotypes",
"Alternate allele frequency",
"Minor allele frequency"
),
# NOTE: currently, object: 'info(VCFHeader)' must be a 3 column
# DataFrame with names Number, Type, Description
# However, VCF 4.2 mentions two more fields: Source, Version
#Source = rep("TVTB", 5),
#Version = rep(packageVersion("TVTB"), 5),
row.names = suffix(param)[c("ref", "het", "alt", "aaf", "maf")]
)
# Collate new data
newInfoData <- DataFrame(REF, HET, ALT, AAF, MAF)
colnames(newInfoData) <- rownames(newInfoHeader)
# Append new header fields
info(header(vcf)) <- rbind(info(header(vcf)), newInfoHeader)
# Append new data fields
info(vcf) <- cbind(
info(vcf),
newInfoData
)
return(vcf)
}
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