cross.
We require chromosome
assignments for the genetic markers, and assume that markers are in
their correct order.readMWril(dir="", rilfile, founderfile,
type=c("ri4self", "ri4sib", "ri8self", "ri8selfIRIP1", "ri8sib", "bgmagic16"),
na.strings=c("-","NA"), rotate=FALSE, ...)"/") or double backslashes
("\\") to specify directory trees."csv"
format described in the help file for read.cross.rilfile, but with just marker names and the
founders' marker genotypes.csv formats, these are interpreted globally
for the entire
file, so missing value codes in phenotypes must not be valid
genotypes, and vice versa.rilfile and founderfile are
rotated (really transposed), with rows corresponding to markers
and columns corresponding to individuals.read.table in the case of
csv and csvr formats. In particular, one may use the
argument
sep to scross; see the help file for
read.cross for details. An additional component crosses is included; this is a matrix
indicating the crosses used to generate the RIL.
rilfile should include a phenotype cross containing
character strings of the form ABCDEFGH, indicating the cross
used to generate each RIL. The founder strains in the founderfile should be the strains
A, B, C, ..., as indicated in the cross
phenotype.
read.cross, sim.crossril <- read.cross("../Data", "ril_data.csv", "founder_geno.csv", "ri4self",
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