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qtl2 (version 0.36)

rbind.scan1: Join genome scan results for different chromosomes.

Description

Join multiple scan1() results for different chromosomes; must have the same set of lod score column.

Usage

# S3 method for scan1
rbind(...)

Value

An object of class `"scan1", like the inputs, but with the results for different sets of chromosomes combined.

Arguments

...

Genome scan objects of class "scan1", as produced by scan1(). Must have the same lod score columns.

Details

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.

See Also

cbind.scan1(), scan1()

Examples

Run this code
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)

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