allchrsplits(cross, chr, error.prob=0.0001, map.function=c("haldane","kosambi","c-f","morgan"), m=0, p=0, maxit=4000, tol=1e-6, sex.sp=TRUE, verbose=TRUE)
cross
. See
read.cross
for details.-
to have all chromosomes but those considered. A logical (TRUE/FALSE)
vector may also be used."scanone"
, so that
one may use plot.scanone
,
summary.scanone
, etc.) with each row being an interval
at which a split is made.
The first two columns are the chromosome ID and midpoint of the interval. The third
column is a LOD score comparing the combined linkage group to the
split into two linkage groups. A fourth column (gap
) indicates the length of
each interval.The row names indicate the flanking markers for each interval.
est.map
, ripple
,
est.rf
, switch.order
,
movemarker
data(fake.bc)
allchrsplits(fake.bc, 7, error.prob=0, verbose=FALSE)
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