seq.all.mrk <- make_seq_mappoly(hexafake, 'all')
id <- get_genomic_order(seq.all.mrk)
s <- make_seq_mappoly(id)
seq10 <- make_seq_mappoly(hexafake, s$seq.mrk.names[1:10])
twopt <- est_pairwise_rf(seq10)
## Using the first 10 markers
l10.seq.3.0 <- ls_linkage_phases(input.seq = seq10, thres = 3, twopt = twopt)
l10.seq.3.0
plot(l10.seq.3.0)
l10.seq.2.0 <- ls_linkage_phases(input.seq = seq10, thres = 2.0, twopt = twopt)
l10.seq.2.0
plot(l10.seq.2.0)
l10.seq.1.0 <- ls_linkage_phases(input.seq = seq10, thres = 1.0, twopt = twopt)
l10.seq.1.0
plot(l10.seq.1.0)
## Using the first 5 markers
seq5 <- make_seq_mappoly(hexafake, s$seq.mrk.names[1:5])
l5.seq.5.0 <- ls_linkage_phases(input.seq = seq5, thres = 5, twopt = twopt)
l5.seq.5.0
plot(l5.seq.5.0)
l5.seq.3.0 <- ls_linkage_phases(input.seq = seq5, thres = 3, twopt = twopt)
l5.seq.3.0
plot(l5.seq.3.0)
l5.seq.1.0 <- ls_linkage_phases(input.seq = seq5, thres = 1, twopt = twopt)
l5.seq.1.0
plot(l5.seq.1.0)
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