locateXO(cross, chr, full.info=FALSE)
cross
. See
read.cross
for details.full.info=TRUE
, in place of a numeric vector with estimated
locations, there is a matrix that includes those locations, the left
and right endpoints of the intervals to which crossovers can be
placed, the marker indices corresponding to those endpoint, and
genotype codes for the genotypes to the left and right of each crossover. The
final column indicates the number of typed markers between the current
crossover and the next one (useful for identifying potential
genotyping errors).
countXO
, cleanGeno
data(hyper)
xoloc <- locateXO(hyper, chr=4)
table(sapply(xoloc, length))
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