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## test pedigree from bioinformatics manuscript
## try x-chrom kinship
## also has inbreeding and twins, for quick check
require(kinship2)
ped2mat <- matrix(c(1,1,0,0,1,
1,2,0,0,2,
1,3,1,2,1,
1,4,1,2,2,
1,5,0,0,2,
1,6,0,0,1,
1,7,3,5,2,
1,8,6,4,1,
1,9,6,4,1,
1,10,8,7,2),ncol=5,byrow=TRUE)
ped2df <- as.data.frame(ped2mat)
names(ped2df) <- c("fam", "id", "dad", "mom", "sex")
## 1 2 3 4 5 6 7 8 9 10,11,12,13,14,15,16
ped2df$disease= c(NA,NA,1,0,0,0,0,1,1,1)
ped2df$smoker= c(0,NA,0,0,1,1,1,0,0,0)
ped2df$availstatus=c(0,0, 1,1,0,1,1,1,1,1)
ped2df$vitalstatus=c(1,1, 1,0,1,0,0,0,0,0)
ped2 <- with(ped2df, pedigree(id, dad, mom, sex, status=vitalstatus,
affected=cbind(disease,smoker, availstatus), relation=matrix(c(8,9,1),ncol=3)))
## regular kinship matrix
kinship(ped2)
kinship(ped2, chr="X")
ped2$sex[9] <- "unknown"
## regular again, should be same as above
kinship(ped2)
## now with unknown sex, gets NAs
kinship(ped2, chrtype="X")
ped2$sex[9]="unknown"
kinship(ped2, chrtype="x")
# all descendants of sex=unknown to be NAs as well
ped2$sex[8]="unknown"
kinship(ped2, chr="X")
## testing kinship2 on pedigreeList when only one subject in a family
peddf <- rbind(ped2df, c(2,1,0,0,1,1,0,1,0))
peds <- with(peddf, pedigree(id, dad, mom, sex, status=vitalstatus,fam=fam,
affected=cbind(disease,smoker, availstatus)))
kinfam <- kinship(peds)
kinfam
## now add two more for ped2, and check again
peddf <- rbind(peddf, c(2,2,0,0,2,1,0,1,0),c(2,3,1,2,1,1,0,1,0))
peds <- with(peddf, pedigree(id, dad, mom, sex, status=vitalstatus,fam=fam,
affected=cbind(disease,smoker, availstatus)))
kin2fam <- kinship(peds)
kin2fam
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