Created
May 2, 2018 16:59
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change_triplet <- c( | |
"C>A:ACA","C>A:ACC","C>A:ACG","C>A:ACT","C>A:CCA","C>A:CCC","C>A:CCG", | |
"C>A:CCT","C>A:GCA","C>A:GCC","C>A:GCG","C>A:GCT","C>A:TCA","C>A:TCC", | |
"C>A:TCG","C>A:TCT","C>G:ACA","C>G:ACC","C>G:ACG","C>G:ACT","C>G:CCA", | |
"C>G:CCC","C>G:CCG","C>G:CCT","C>G:GCA","C>G:GCC","C>G:GCG","C>G:GCT", | |
"C>G:TCA","C>G:TCC","C>G:TCG","C>G:TCT","C>T:ACA","C>T:ACC","C>T:ACG", | |
"C>T:ACT","C>T:CCA","C>T:CCC","C>T:CCG","C>T:CCT","C>T:GCA","C>T:GCC", | |
"C>T:GCG","C>T:GCT","C>T:TCA","C>T:TCC","C>T:TCG","C>T:TCT","T>A:ATA", | |
"T>A:ATC","T>A:ATG","T>A:ATT","T>A:CTA","T>A:CTC","T>A:CTG","T>A:CTT", | |
"T>A:GTA","T>A:GTC","T>A:GTG","T>A:GTT","T>A:TTA","T>A:TTC","T>A:TTG", | |
"T>A:TTT","T>C:ATA","T>C:ATC","T>C:ATG","T>C:ATT","T>C:CTA","T>C:CTC", | |
"T>C:CTG","T>C:CTT","T>C:GTA","T>C:GTC","T>C:GTG","T>C:GTT","T>C:TTA", | |
"T>C:TTC","T>C:TTG","T>C:TTT","T>G:ATA","T>G:ATC","T>G:ATG","T>G:ATT", | |
"T>G:CTA","T>G:CTC","T>G:CTG","T>G:CTT","T>G:GTA","T>G:GTC","T>G:GTG", | |
"T>G:GTT","T>G:TTA","T>G:TTC","T>G:TTG","T>G:TTT" | |
) | |
revcomp <- function(s) { | |
return(as.character(reverseComplement(DNAString(s)))) | |
} | |
isBadGeno <- function(genoIndex) { | |
if(isGenoIndexRef(genoIndex)){return(FALSE)} | |
if("." %in% genoIndex){return(TRUE)} | |
if(length(genoIndex) > 2){return(TRUE)} | |
return(FALSE) | |
} | |
isGenoIndexRef <- function(genoIndex) { | |
if(length(genoIndex) == 0){return(TRUE)} | |
return(length(genoIndex) == 1 | |
&& (genoIndex[[1]] == "." || genoIndex[[1]] == "0")) | |
} | |
getFirstGenoAltIndex <- function(genoIndex) { | |
return(Filter(function(x)x!="0",genoIndex)[1]) | |
} | |
genOpportunityFromGenome <- function(bsgenome, target_regions, nsamples=1) { | |
# make sure there are no overlaps | |
target_regions <- reduce(target_regions, drop.empty.ranges=TRUE) | |
# count the kmers in the region | |
kmers <- colSums(oligonucleotideFrequency( | |
getSeq(bsgenome, target_regions),3)) | |
# turn back into matrix | |
c0 <- names(kmers) | |
dim(kmers) <- c(1, length(kmers)) | |
colnames(kmers) <- c0 | |
uk <- sapply(colnames(kmers), | |
function(x){y<-substr(x,2,2);if(y=="C"||y=="T"){x}else{revcomp(x)}}) | |
m <- matrix(0, nrow=1, ncol=length(change_triplet)) | |
colnames(m) <- change_triplet | |
for(i in 1:length(kmers)) { | |
v <- kmers[i] | |
k <- uk[[i]] | |
for(j in grep(k,change_triplet)) { | |
m[1,j] = v + m[1,j] | |
} | |
} | |
# replicate the matrix over the number of desired samples | |
m <- do.call("rbind",rep(list(m),nsamples)) | |
return(m) | |
} | |
genCountMatrixFromVcf <- function(bsgenome, vcfobj) { | |
# keep only SNVs | |
vcfobj <- vcfobj[isSNV(vcfobj),] | |
contexts <- getSeq(bsgenome, resize(granges(vcfobj), 3, fix="center")) | |
alts <- alt(vcfobj) | |
refs <- ref(vcfobj) | |
gtsMat = geno(vcfobj)$GT | |
gtsMat = structure(sapply(strsplit(gtsMat,"/",fixed=T), unique), dim=dim(gtsMat)) | |
sample_names <- colnames(vcfobj) | |
count_matrix <- matrix(0, | |
nrow=length(sample_names), ncol=length(change_triplet)) | |
rownames(count_matrix) <- sample_names | |
colnames(count_matrix) <- change_triplet | |
for(i in 1:nrow(gtsMat)) { | |
rb <- refs[[i]] | |
cc <- contexts[i] | |
if(rb == DNAString("C") || rb == DNAString("T")) { | |
cts = sapply(alts[i], function(ab){paste0(rb,">",ab,":",cc)}) | |
} else { | |
cts = sapply(alts[i], function(ab){ | |
paste0(reverseComplement(rb),">", | |
reverseComplement(ab),":", | |
reverseComplement(cc))}) | |
} | |
for(j in 1:length(sample_names)) { | |
gi = gtsMat[[i,j]] | |
if(isGenoIndexRef(gi)) {next} | |
if(isBadGeno(gi)){ | |
warning(paste0("Genotype of Line ",i," sample ", | |
sample_names[j]," is not supported, it will be skipped.")) | |
next | |
} | |
ai <- as.integer(getFirstGenoAltIndex(gi)) | |
ct <- cts[[ai]] | |
cx <- match(ct, change_triplet) | |
if(is.na(cx)) { | |
warning(paste0("ct = ",ct)) | |
next | |
} | |
count_matrix[j,cx] = 1 + count_matrix[j,cx] | |
} | |
} | |
return(count_matrix) | |
} | |
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