aboutsummaryrefslogtreecommitdiff
path: root/scripts
diff options
context:
space:
mode:
authorzsloan2022-03-22 20:39:22 +0000
committerzsloan2022-03-22 20:39:22 +0000
commita75634cc5637168165e601f09dc9ad820e6e443f (patch)
treea81c350a5a08b3b7cdf8375b728b48951791a14c /scripts
parent0e6990940e22eb0431d6a27e45d29bc04d8ad582 (diff)
parent8c77af63efae6f06d7c7c3269fc0e41811a8037a (diff)
downloadgenenetwork3-a75634cc5637168165e601f09dc9ad820e6e443f.tar.gz
Merge branch 'feature/add_rqtl_pairscan' of https://github.com/zsloan/genenetwork3 into feature/add_rqtl_pairscan
Diffstat (limited to 'scripts')
-rw-r--r--scripts/rqtl_wrapper.R95
1 files changed, 49 insertions, 46 deletions
diff --git a/scripts/rqtl_wrapper.R b/scripts/rqtl_wrapper.R
index 5ecd774..ea2c345 100644
--- a/scripts/rqtl_wrapper.R
+++ b/scripts/rqtl_wrapper.R
@@ -178,6 +178,9 @@ if (!is.null(opt$pairscan)) {
} else if (!is.null(opt$interval)) {
verbose_print('Calculating genotype probabilities with interval mapping\n')
cross_object <- calc.genoprob(cross_object, step=5, stepwidth="max")
+} else if (!is.null(opt$pairscan)) {
+ verbose_print('Calculating genotype probabilities for pair-scan\n')
+ cross_object <- calc.genoprob(cross_object, step=10)
} else {
verbose_print('Calculating genotype probabilities\n')
cross_object <- calc.genoprob(cross_object)
@@ -294,57 +297,57 @@ if (!is.null(opt$addcovar) || !is.null(opt$control)){
qtl_results = scan_func(cross_object, pheno.col=1, model=opt$model, method=opt$method)
}
-#QTL main effects on adjusted longevity
-getEffects <- function(sdata, gtsprob, marker = "1_24042124", model = "longevity ~ sex + site + cohort + treatment", trait = "longevity"){
- rownames(sdata) <- 1:nrow(sdata)
- rownames(gtsprob) <- 1:nrow(gtsprob)
- mp <- gtsprob[, grep(marker, colnames(gtsprob))]
- gts <- unlist(lapply(lapply(lapply(apply(mp,1,function(x){which(x > 0.85)}),names), strsplit, ":"), function(x){
- if(length(x) > 0){ return(x[[1]][2]); }else{ return(NA) }
- }))
-
- ismissing <- which(apply(sdata, 1, function(x){any(is.na(x))}))
- if(length(ismissing) > 0){
- sdata <- sdata[-ismissing, ]
- gts <- gts[-ismissing]
- }
-
- mlm <- lm(as.formula(model), data = sdata)
- pheAdj <- rep(NA, nrow(sdata))
- adj <- residuals(mlm) + mean(sdata[, trait])
- pheAdj[as.numeric(names(adj))] <- adj
- means <- c(mean(pheAdj[which(gts == "AC")],na.rm=TRUE),mean(pheAdj[which(gts == "AD")],na.rm=TRUE),mean(pheAdj[which(gts == "BC")],na.rm=TRUE),mean(pheAdj[which(gts == "BD")],na.rm=TRUE))
- std <- function(x) sd(x,na.rm=TRUE)/sqrt(length(x))
- stderrs <- c(std(pheAdj[which(gts == "AC")]),std(pheAdj[which(gts == "AD")]),std(pheAdj[which(gts == "BC")]),std(pheAdj[which(gts == "BD")]))
- paste0(round(means,0), " ± ", round(stderrs,2))
-}
-
-if (type == "4-way") {
- verbose_print("Get phenotype name + genoprob + all phenotypes + models for 4-way crosses")
- traitname <- colnames(pull.pheno(cross_object))[1]
- gtsp <- pull.genoprob(cross_object)
- allpheno <- pull.pheno(cross_object)
- if (!is.null(opt$addcovar)) {
- model <- paste0(traitname, " ~ ", paste0(covar_names, sep="", collapse=" + "))
- } else {
- model <- paste0(traitname, " ~ 1 ")
- }
-
- meffects <- c()
- verbose_print("Getting QTL main effects for 4-way crosses")
- for(marker in rownames(qtl_results)){
- meff <- getEffects(allpheno, gtsp, marker = marker, model, trait = traitname)
- meffects <- rbind(meffects, meff)
- }
- qtl_results <- cbind(data.frame(qtl_results[,1:3]), meffects)
- colnames(qtl_results)[4:7] <- c("AC", "AD", "BC", "BD")
-}
-
verbose_print('Writing results to CSV file\n')
if (!is.null(opt$pairscan)) {
map_out_file = file.path(opt$outdir, paste("MAP_", opt$filename, sep = "" ))
write.csv(qtl_results[1], out_file)
write.csv(qtl_results[2], map_out_file)
} else {
+ # QTL main effects on adjusted longevity
+ getEffects <- function(sdata, gtsprob, marker = "1_24042124", model = "longevity ~ sex + site + cohort + treatment", trait = "longevity"){
+ rownames(sdata) <- 1:nrow(sdata)
+ rownames(gtsprob) <- 1:nrow(gtsprob)
+ mp <- gtsprob[, grep(marker, colnames(gtsprob))]
+ gts <- unlist(lapply(lapply(lapply(apply(mp,1,function(x){which(x > 0.85)}),names), strsplit, ":"), function(x){
+ if(length(x) > 0){ return(x[[1]][2]); }else{ return(NA) }
+ }))
+
+ ismissing <- which(apply(sdata, 1, function(x){any(is.na(x))}))
+ if(length(ismissing) > 0){
+ sdata <- sdata[-ismissing, ]
+ gts <- gts[-ismissing]
+ }
+
+ mlm <- lm(as.formula(model), data = sdata)
+ pheAdj <- rep(NA, nrow(sdata))
+ adj <- residuals(mlm) + mean(sdata[, trait])
+ pheAdj[as.numeric(names(adj))] <- adj
+ means <- c(mean(pheAdj[which(gts == "AC")],na.rm=TRUE),mean(pheAdj[which(gts == "AD")],na.rm=TRUE),mean(pheAdj[which(gts == "BC")],na.rm=TRUE),mean(pheAdj[which(gts == "BD")],na.rm=TRUE))
+ std <- function(x) sd(x,na.rm=TRUE)/sqrt(length(x))
+ stderrs <- c(std(pheAdj[which(gts == "AC")]),std(pheAdj[which(gts == "AD")]),std(pheAdj[which(gts == "BC")]),std(pheAdj[which(gts == "BD")]))
+ paste0(round(means,0), " ± ", round(stderrs,2))
+ }
+
+ if (type == "4-way") {
+ verbose_print("Get phenotype name + genoprob + all phenotypes + models for 4-way crosses")
+ traitname <- colnames(pull.pheno(cross_object))[1]
+ gtsp <- pull.genoprob(cross_object)
+ allpheno <- pull.pheno(cross_object)
+ if (!is.null(opt$addcovar)) {
+ model <- paste0(traitname, " ~ ", paste0(covar_names, sep="", collapse=" + "))
+ } else {
+ model <- paste0(traitname, " ~ 1 ")
+ }
+
+ meffects <- c()
+ verbose_print("Getting QTL main effects for 4-way crosses")
+ for(marker in rownames(qtl_results)){
+ meff <- getEffects(allpheno, gtsp, marker = marker, model, trait = traitname)
+ meffects <- rbind(meffects, meff)
+ }
+ qtl_results <- cbind(data.frame(qtl_results[,1:3]), meffects)
+ colnames(qtl_results)[4:7] <- c("AC", "AD", "BC", "BD")
+ }
+
write.csv(qtl_results, out_file)
}