Difference between revisions of "Family-based Association Exercise"
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==Family-based Association Exercise== | ==Family-based Association Exercise== | ||
| − | + | cd exercises/cordell/FASTLMM_GCTA | |
| − | cd exercises/cordell/FASTLMM_GCTA | + | ls -l |
| − | ls -l | + | plink --bfile quantfamdata --assoc --out plinkresults |
| − | plink --bfile quantfamdata --assoc --out plinkresults | + | R |
| − | R | + | res1<-read.table("plinkresults.qassoc", header=T) |
| − | res1<-read.table("plinkresults.qassoc", header=T) | + | head(res1) |
| − | head(res1) | + | source("qqmanHJCupdated.R") |
| − | source("qqmanHJCupdated.R") | + | manhattan(res1, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5) |
| − | manhattan(res1, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5) | + | qq(res1$P) |
| − | qq(res1$P) | + | chi<-(qchisq(1-res1$P,1)) |
| − | chi<-(qchisq(1-res1$P,1)) | + | lambda=median(chi)/0.456 |
| − | lambda=median(chi)/0.456 | + | lambda |
| − | lambda | + | fastlmmc -bfile quantfamdata -pheno quantfamdata.fam -mpheno 4 -bfileSim quantfamdata -ML -out FLMMresults |
| − | fastlmmc -bfile quantfamdata -pheno quantfamdata.fam -mpheno 4 -bfileSim quantfamdata -ML -out FLMMresults | + | R |
| − | R | + | res2<-read.table("FLMMresults", header=T) |
| − | res2<-read.table("FLMMresults", header=T) | + | head(res2) |
| − | head(res2) | + | chi<-(qchisq(1-res2$Pvalue,1)) |
| − | chi<-(qchisq(1-res2$Pvalue,1)) | + | lambda=median(chi)/0.456 |
| − | lambda=median(chi)/0.456 | + | lambda |
| − | lambda | + | new<-data.frame(res2$SNP, res2$Chromosome, res2$Position, res2$Pvalue) |
| − | new<-data.frame(res2$SNP, res2$Chromosome, res2$Position, res2$Pvalue) | + | names(new)<-c("SNP", "CHR", "BP", "P") |
| − | names(new)<-c("SNP", "CHR", "BP", "P") | + | head(new) |
| − | head(new) | + | qq(new$P) |
| − | qq(new$P) | + | manhattan(new, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5) |
| − | manhattan(new, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5) | + | |
Revision as of 18:49, 23 January 2019
Family-based Association Exercise
cd exercises/cordell/FASTLMM_GCTA
ls -l
plink --bfile quantfamdata --assoc --out plinkresults
R
res1<-read.table("plinkresults.qassoc", header=T)
head(res1)
source("qqmanHJCupdated.R")
manhattan(res1, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5)
qq(res1$P)
chi<-(qchisq(1-res1$P,1))
lambda=median(chi)/0.456
lambda
fastlmmc -bfile quantfamdata -pheno quantfamdata.fam -mpheno 4 -bfileSim quantfamdata -ML -out FLMMresults
R
res2<-read.table("FLMMresults", header=T)
head(res2)
chi<-(qchisq(1-res2$Pvalue,1))
lambda=median(chi)/0.456
lambda
new<-data.frame(res2$SNP, res2$Chromosome, res2$Position, res2$Pvalue)
names(new)<-c("SNP", "CHR", "BP", "P")
head(new)
qq(new$P)
manhattan(new, pch=20, suggestiveline=F, genomewideline=F, ymin=2, cex.x.axis=0.65, colors=c("black","dodgerblue"), cex=0.5)
