Join genome scan results for different chromosomes.
Join multiple scan1() results for different
chromosomes; must have the same set of lod score column.
## S3 method for class 'scan1' rbind(...)
... |
Genome scan objects of class |
If components addcovar, Xcovar,
intcovar, weights, sample_size do not match
between objects, we omit this information.
If hsq present, we simply rbind() the contents.
An object of class '"scan1", like the inputs, but with the results for different sets of chromosomes combined.
grav2 <- read_cross2(system.file("extdata", "grav2.zip", package="qtl2"))
map <- insert_pseudomarkers(grav2$gmap, step=1)
probs <- calc_genoprob(grav2, map, error_prob=0.002)
phe <- grav2$pheno[,1,drop=FALSE]
out1 <- scan1(probs[,1], phe) # chr 1
out2 <- scan1(probs[,5], phe) # chr 5
out <- rbind(out1, out2)Please choose more modern alternatives, such as Google Chrome or Mozilla Firefox.