Description Usage Arguments Value Note
New_sampling
uses the output of Infection_Sim
and Sequencing
to sample a selection of sequences and write the annotated output top file as a fasta
1 2 3 4 |
sim.out |
Output of |
seq.out |
Output of |
file |
Directory path where the nexus file of samples are to be saved to. |
n.seq.samples |
Number of sequences to be sampled in total |
bs.label |
String used to be added on to the created nex files. Default = "bs" |
sigma |
The interval parameter, where the interval of sequences is equal to 1/sigma. Default = 1, i.e. all sequences |
n.bs |
Number of bootstrap samples to create. Default = 50 |
oldestboolean |
Boolean if the oldest sample is included (TRUE). Default=TRUE |
outgroup |
Boolean if the outgroup is included (TRUE). Default=FALSE |
discretised |
Boolean if discretised sampling occurs. Default = FALSE |
proportional |
Boolean if proportional sampling occurs. Default = FALSE |
t.cont |
Boolean if the simulation occurs in discrete (FALSE) or continuous time (TRUE), in turn directing whether decimilisation is needed in uniform sampling strategies. |
missed.generations |
Number of intiial generations not considered for sampling. Default = 0 |
save a nexus file of dated sequences
If the combination of prop.times and extant==FALSE creates a time window that does not include all clades, and all.clades == TRUE, only all the possible clades within the time window will be sampled.
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