Difference between revisions of "GWAS Data QC Exercise"

From Statistical Genetics Courses

Jump to: navigation, search
 
Line 1: Line 1:
 +
__NOTITLE__
 +
 +
==GWAS Data QC Exercise==
 
<pre> plink --file GWAS --noweb
 
<pre> plink --file GWAS --noweb
 
  plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind --noweb
 
  plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind --noweb

Latest revision as of 15:34, 7 June 2018

GWAS Data QC Exercise

 plink --file GWAS --noweb
 plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind --noweb
 plink --file GWAS_clean_mind --maf 0.05 --recode --out MAF_greater_5 --noweb
 plink --file GWAS_clean_mind --exclude MAF_greater_5.map --recode --out MAF_less_5 --noweb
 plink --file MAF_greater_5 --geno 0.05 --recode --out MAF_greater_5_clean --noweb
 plink --file MAF_less_5 --geno 0.01 --recode --out MAF_less_5_clean --noweb
 plink --file MAF_greater_5_clean --merge MAF_less_5_clean.ped MAF_less_5_clean.map --recode --out GWAS_MAF_clean --noweb
 plink --file GWAS_MAF_clean --mind 0.03 --recode --out GWAS_clean2 --noweb
 plink --file GWAS_clean2 --check-sex --out GWAS_sex_checking --noweb
 
R:
 sexcheck = read.table("GWAS_sex_checking.sexcheck", header=T)
 names(sexcheck)
 sex_problem = sexcheck[which(sexcheck$STATUS=="PROBLEM"),]
 sex_problem
 q()
 plink --file GWAS_clean2 --genome --out duplicates --noweb
 
R:
 dups = read.table("duplicates.genome", header = T)
 problem_pairs = dups[which(dups$PI_HAT > 0.4),]
 problem_pairs
 problem_pairs = dups[which(dups$PI_HAT > 0.05),]
 myvars = c("FID1", "IID1", "FID2", "IID2", "PI_HAT")
 problem_pairs[myvars]
 q()
 plink --file GWAS_clean2 --remove IBS_excluded.txt --recode --out GWAS_clean3 --noweb
 plink --file GWAS_clean3 --het --noweb
 
R:
 Dataset <- read.table("plink.het", header=TRUE, sep="", na.strings="NA", dec=".",
 strip.white=TRUE)
 mean(Dataset$F)
 sd(Dataset$F)
 jpeg("hist.jpeg", height=1000, width=1000)
 hist(scale(Dataset$F), xlim=c(-4,4))
 dev.off()
 q()
 plink --file GWAS_clean3 --pheno pheno.txt --pheno-name Aff --hardy --noweb
 
R:
 hardy = read.table("plink.hwe", header = T)
 names(hardy)
 hwe_prob = hardy[which(hardy$P < 0.0000009),]
 hwe_prob
 q()
 plink --file GWAS_clean3 --exclude HWE_out.txt --recode --out GWAS_clean4 --noweb==GWAS Control Substructure==
 plink --file GWAS_clean4 --genome --mds-plot 10 --noweb
 
R:
 mydata = read.table("mds_components.txt", header=T)
 mydata$pch[mydata$Group==1 ] <-15
 mydata$pch[mydata$Group==2 ] <-16
 mydata$pch[mydata$Group==3 ] <-2
 jpeg("mds.jpeg", height=1000, width=1000)
 plot(mydata$C1, mydata$C2 ,pch=mydata$pch)
 dev.off()
 q()
 plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --logistic --adjust --out unadj --noweb
 plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --covar plink.mds --covar-name C1 --logistic --adjust --out C1 --noweb
 plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --covar plink.mds --covar-name C1-C2 --logistic --adjust --out C1-C2 --noweb
 
R:
 broadqq <-function(pvals, title)
 {
     observed <- sort(pvals)
     lobs <- -(log10(observed))
     expected <- c(1:length(observed))
     lexp <- -(log10(expected / (length(expected)+1)))
     plot(c(0,7), c(0,7), col="red", lwd=3, type="l", xlab="Expected (-logP)", ylab="Observed (-logP)", xlim=c(0,max(lobs)), ylim=c(0,max(lobs)), las=1, xaxs="i", yaxs="i", bty="l", main = title)
     points(lexp, lobs, pch=23, cex=.4, bg="black") }
 jpeg("qqplot_compare.jpeg", height=1000, width=1000)
 par(mfrow=c(2,1))
 aff_unadj<-read.table("unadj.assoc.logistic", header=TRUE)
 aff_unadj.add.p<-aff_unadj[aff_unadj$TEST==c("ADD"),]$P
 broadqq(aff_unadj.add.p,"Some Trait Unadjusted")
 aff_C1C2<-read.table("C1-C2.assoc.logistic", header=TRUE)
 aff_C1C2.add.p<-aff_C1C2[aff_C1C2$TEST==c("ADD"),]$P
 broadqq(aff_C1C2.add.p, "Some Trait Adjusted")
 dev.off()
 gws_unadj = aff_unadj[which(aff_unadj$P < 0.0000001),]
 gws_unadj
 gws_adjusted = aff_C1C2[which(aff_C1C2$P < 0.0000001),]
 gws_adjusted
 q()