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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