Difference between revisions of "AdvGeneMap2018Commands"
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===Plink - Part 1 - Data QC=== | ===Plink - Part 1 - Data QC=== | ||
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plink --file GWAS | plink --file GWAS | ||
plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind | plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind | ||
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plink --file GWAS_clean3 --het | plink --file GWAS_clean3 --het | ||
###### in R | ###### in R | ||
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===Plink - Part 2 - Controlling for Substructure=== | ===Plink - Part 2 - Controlling for Substructure=== | ||
| + | <nowiki> | ||
plink --file GWAS_clean4 --genome --cluster --mds-plot 10 | plink --file GWAS_clean4 --genome --cluster --mds-plot 10 | ||
#### in R | #### in R | ||
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gws_adjusted = aff_C1C2[which(aff_C1C2$P < 0.0000001),] | gws_adjusted = aff_C1C2[which(aff_C1C2$P < 0.0000001),] | ||
gws_adjusted | gws_adjusted | ||
| + | <nowiki> | ||
Revision as of 15:00, 23 January 2018
Plink - Part 1 - Data QC
plink --file GWAS
plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind
plink --file GWAS_clean_mind --maf 0.05 --recode --out MAF_greater_5
plink --file GWAS_clean_mind --exclude MAF_greater_5.map --recode --out MAF_less_5
plink --file MAF_greater_5 --geno 0.05 --recode --out MAF_greater_5_clean
plink --file MAF_less_5 --geno 0.01 --recode --out MAF_less_5_clean
plink --file MAF_greater_5_clean --merge MAF_less_5_clean.ped MAF_less_5_clean.map --recode --out GWAS_MAF_clean
plink --file GWAS_MAF_clean --mind 0.03 --recode --out GWAS_clean2
plink --file GWAS_clean2 --check-sex --out GWAS_sex_checking
#### in R - open R by simply typing R
setwd("to_your_working_directory/")
sexcheck = read.table("GWAS_sex_checking.sexcheck", header=T)
names(sexcheck)
sex_problem = sexcheck[which(sexcheck$STATUS=="PROBLEM"),]
sex_problem
q()
##################################
plink --file GWAS_clean2 --genome --out duplicates
#### in R
setwd("to_your_working_directory/")
dups = read.table("duplicates.genome", header = T)
problem_pairs = dups[which(dups$PI_HAT > 0.4),]
problem_pairs
problem_pairs = dups[which(dups$PI_HAT > 0.05),]
myvars = c("FID1", "IID1", "FID2", "IID2", "PI_HAT")
problem_pairs[myvars]
q()
######
plink --file GWAS_clean2 --remove IBS_excluded.txt --recode --out GWAS_clean3
plink --file GWAS_clean3 --het
###### in R
Dataset
Plink - Part 2 - Controlling for Substructure
plink --file GWAS_clean4 --genome --cluster --mds-plot 10 #### in R mydata = read.table("mds_components.txt", header=T) mydata$pch[mydata$Group==1 ] <-15 mydata$pch[mydata$Group==2 ] <-16 mydata$pch[mydata$Group==3 ] <-2 jpeg("mds.jpeg", height=500, width=500) plot(mydata$C1, mydata$C2 ,pch=mydata$pch) dev.off() q() ###### plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --logistic --adjust --out unadj plink --file GWAS_clean4 --genome --cluster --pca 10 header plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --covar plink.eigenvec --covar-name PC1 --logistic --adjust --out PC1 plink --file GWAS_clean4 --pheno pheno.txt --pheno-name Aff --covar plink.eigenvec --covar-name PC1-PC2 --logistic --adjust --out PC1-PC2 #### in 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=500) 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("PC1-PC2.assoc.logistic", header=TRUE) aff_C1C2.add.p<-aff_C1C2[aff_C1C2$TEST==c("ADD"),]$P broadqq(aff_C1C2.add.p, "Some Trait Adjusted for PC1 and PC2") 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 <nowiki>
