Nothing
data(minnbreast)
mbsub <- minnbreast[minnbreast$famid %in% c(4, 42, 165, 432),]
PedDf <- mbsub[, c("famid", "id", "fatherid", "motherid", "sex")]
colnames(PedDf) <- FamAgg:::.PEDCN
PedDf$sex <- FamAgg:::sanitizeSex(PedDf$sex)
## data(minnbreast)
## mbsub <- minnbreast[minnbreast$famid %in% 4:19, ]
## PedDf <- mbsub[, c("famid", "id", "fatherid", "motherid", "sex")]
## colnames(PedDf) <- FamAgg:::.PEDCN
## PedDf$sex <- FamAgg:::sanitizeSex(PedDf$sex)
## generate the FAData.
fad <- FAData(pedigree=PedDf)
## specify the trait.
tcancer <- mbsub$cancer
names(tcancer) <- mbsub$id
## OK, 0.0.6
## evaluating the kinship analysis method and for FAKinshipResult objects.
test_kinship_group <- function(){
##
## run the analysis.
set.seed(18011977)
far <- kinshipGroupTest(fad, trait=tcancer, traitName="cancer",
nsim=500)
## repeating the test and evaluate whether we get the same results.
set.seed(18011977)
far2 <- kinshipGroupTest(fad, trait=tcancer, traitName="cancer",
nsim=500)
checkEquals(far, far2)
## replacing the trait with a random trait.
tpreg <- mbsub$everpreg
names(tpreg) <- mbsub$id
## randomizing to see if re-ordering works...
tpregrand <- sample(tpreg, length(tpreg))
trait(far) <- tpregrand
checkEquals(trait(far), tpreg)
## testing to subset the object... which is not supported
checkException(far[1:10, ])
return(TRUE)
}
## question if for the plotting: how to build the pedigree: just the pheno and aff
## from the affectedKinshipGroups?
## plot the kinshipGroup.
test_plot_kinship <- function(){
do.plot <- FALSE
set.seed(18011977)
far <- kinshipGroupTest(fad, trait=tcancer, traitName="cancer", nsim=500)
res <- result(far)
res <- res[order(res$kinship_pvalue), ]
if(do.plot){
switchPlotfun("ks2paint")
plotPed(far, id="17517", prune=TRUE, device="plot", cex=0.4)
plotPed(far, id="17517", prune=FALSE, device="plot")
}
## switchPlotfun()
}
test_buildped_kinship <- function(){
## data(minnbreast)
## mbsub <- minnbreast[minnbreast$famid %in% c(4, 42, 165, 432),]
## PedDf <- mbsub[, c("famid", "id", "fatherid", "motherid", "sex")]
## colnames(PedDf) <- FamAgg:::.PEDCN
## PedDf$sex <- FamAgg:::sanitizeSex(PedDf$sex)
## ## generate the FAData.
## fad <- FAData(pedigree=PedDf)
## ## specify the trait.
## tcancer <- mbsub$cancer
## names(tcancer) <- mbsub$id
set.seed(18011977)
far <- kinshipGroupTest(fad, trait=tcancer, traitName="cancer", nsim=500)
res <- result(far)
res <- res[order(res$kinship_pvalue), ]
FullPed <- buildPed(far, id=res[1, "group_id"])
affGroup <- affectedKinshipGroups(far)[[res[1, "group_id"]]]
allids <- unique(c(affGroup$aff, affGroup$pheno))
## check if all ids are in the pedigree.
checkEquals(length(allids), sum(allids %in% FullPed$id))
## check if the same works for the pruned pedigree:
SmallPed <- buildPed(far, id=res[1, "group_id"], prune=TRUE)
checkEquals(length(allids), sum(allids %in% SmallPed$id))
}
notrun_test_compare_strat_normal <- function(){
## test the strata test and compare that to the "normal" test
set.seed(18011977)
fag <- kinshipGroupTest(fad, trait=tcancer, nsim=500)
fag2 <- fag
set.seed(18011977)
fag2 <- runSimulation(fag2, nsim=500)
## Compare
checkEquals(fag@sim$pvalueRatio, fag2@sim$pvalueRatio)
checkEquals(fag@sim$pvalueKinship, fag2@sim$pvalueKinship)
## now do it with strata = 1.
strat <- rep("A", length(fad$id))
set.seed(18011977)
fag2 <- FamAgg:::runSimulationStrata(fag, nsim=500, strata=strat)
checkEquals(fag@sim$pvalueRatio, fag2@sim$pvalueRatio)
checkEquals(fag@sim$pvalueKinship, fag2@sim$pvalueKinship)
## Test if the NAs are correctly removed...
strat[!is.na(tcancer)][1:10] <- NA
fag2 <- FamAgg:::runSimulationStrata(fag, nsim=500, strata=strat)
## Have to get the message that 10 phenotyped are removed.
## OK, that's it. Now do the same but with sex strata.
fasex <- FamAgg:::runSimulationStrata(fag, nsim=500, strata=fad$sex)
Col <- rep("blue", length(fad$id))
Col[which(fad$sex == "F")] <- "red"
plot(fasex@sim$pvalueKinship, fag@sim$pvalueKinship, xlab="Sex stratified",
ylab="No stratification", col=Col)
abline(0, 1)
}
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