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author | zsloan | 2021-10-14 18:03:50 +0000 |
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committer | zsloan | 2021-10-14 18:03:50 +0000 |
commit | baa801e81c5b0f7c7b30c6ca880a806a6bce54db (patch) | |
tree | 1effb064d8bc1141f01f3f441a29bb32d1c9807d /scripts | |
parent | 1bad61a9fee4cc41636ef4a184d86bd70df5395c (diff) | |
download | genenetwork3-baa801e81c5b0f7c7b30c6ca880a806a6bce54db.tar.gz |
Incorporated Danny's code for calculating QTL main effects into rqtl_wrapper.R
Diffstat (limited to 'scripts')
-rw-r--r-- | scripts/rqtl_wrapper.R | 43 |
1 files changed, 43 insertions, 0 deletions
diff --git a/scripts/rqtl_wrapper.R b/scripts/rqtl_wrapper.R index 20c0e06..523888f 100644 --- a/scripts/rqtl_wrapper.R +++ b/scripts/rqtl_wrapper.R @@ -269,4 +269,47 @@ if (!is.null(opt$addcovar) || !is.null(opt$control)){ verbose_print('Running scanone\n') qtl_results = scanone(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) + model <- paste0(traitname, " ~ ", paste0(covar_names, sep="", collapse=" + ")) + + 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) |