| htr {gap} | R Documentation |
Haplotype trend regression (with permutation)
htr(y, x, n.sim = 0)
y |
a vector of phenotype. |
x |
a haplotype table. |
n.sim |
the number of permutations. |
The returned value is a list containing:
fthe F statistic for overall association
pthe p value for overall association
fvthe F statistics for individual haplotypes
pithe p values for individual haplotypes
adapted from emgi.cpp, a pseudorandom number seed will be added on.
Dimitri Zaykin, Jing Hua Zhao
Zaykin DV, Westfall PH, Young SS, Karnoub MA, Wagner MJ, Ehm MG (2002) Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum. Hered. 53:79-91
Xie R, Stram DO (2005). Asymptotic equivalence between two score tests for haplotype-specific risk in general linear models. Genet. Epidemiol. 29:186-170
## Not run:
# 26-10-03
# this is now part of demo
test2<-read.table("test2.dat")
y<-test2[,1]
x<-test2[,-1]
y<-as.matrix(y)
x<-as.matrix(x)
htr.test2<-htr(y,x)
htr.test2
htr.test2<-htr(y,x,n.sim=10)
htr.test2
# 13-11-2003
require(gap.datasets)
data(apoeapoc)
apoeapoc.gc<-gc.em(apoeapoc[,5:8])
y<-apoeapoc$y
for(i in 1:length(y)) if(y[i]==2) y[i]<-1
htr(y,apoeapoc.gc$htrtable)
# 20-8-2008
# part of the example from useR!2008 tutorial by Andrea Foulkes
# It may be used beyond the generalized linear model (GLM) framework
HaploEM <- haplo.em(Geno,locus.label=SNPnames)
HapMat <- HapDesign(HaploEM)
m1 <- lm(Trait~HapMat)
m2 <- lm(Trait~1)
anova(m2,m1)
## End(Not run)