View source: R/extended_geneplot.R
calc_geneplot_spdfs | R Documentation |
Use before prepare_plot_params and plot_geneplot_spdfs.
calc_geneplot_spdfs(
dat,
refpopnames,
locnames,
includepopnames = NULL,
quantiles_vec,
prior,
logten = T,
saddlepoint = T,
leave_one_out = F,
rel_tol = NULL,
abs_tol = NULL,
npts = 1000
)
dat |
The data, in a data frame, with two columns labelled as 'id' and 'pop', and with two additional columns per locus. Missing data at any locus should be marked as '0' for each allele. The locus columns must be labelled in the format Loc1.a1, Loc1.a2, Loc2.a1, Loc2.a2, etc. Missing data must be for BOTH alleles at any locus. See read_genepop_format for details of how to import Genepop format data files into the appropriate format. |
refpopnames |
Character vector of reference population names, that must
match two values in the 'pop' column of |
locnames |
Character vector, names of the loci, which must match the
column names in the data so e.g. if dat has columns id, pop, EV1.a1,
EV1.a2, EV14.a1, EV14.a2, etc. then you could use 'locnames =
c("EV1","EV14") etc. The locnames do not need to be in any particular order
but all of them must be in |
includepopnames |
Character vector (default NULL) of population names to
be included in the calculations as comparison populations. The reference
populations are automatically used as comparison populations for each
other, but you can also add additional comparison populations using
|
quantiles_vec |
Specify which quantiles to show on the plots, as a vector of numbers between 0 and 1. They do not have to be ordered. If NULL, quantiles will not be plotted. |
prior |
(default "Rannala") String, either "Rannala" or "Baudouin", giving the choice of prior parameter for the Dirichlet priors for the allele frequency estimates. Both options define parameter values that depend on the number of alleles at each locus, k. "Baudouin" gives slightly more weight to rare alleles than "Rannala" does, or less weight to the data, so Baudouin may be more suitable for small reference samples, but there is no major difference between them. For more details, see McMillan and Fewster (2017), Biometrics. Additional options are "Half" or "Quarter" which specify parameters 1/2 or 1/4, respectively. These options have priors whose parameters do not depend on the number of alleles at each locus, and so may be more suitable for microsatellite data with varying numbers of alleles at each locus. |
logten |
(default TRUE) Boolean, indicates whether to use base 10 for the logarithms, or base e (i.e. natural logarithms). logten=TRUE is default because it's easier to recalculate the original non-log numbers in your head when looking at the plots. Use FALSE for natural logarithms. |
saddlepoint |
(default TRUE) If TRUE, use saddlepoint approximation to impute Log-Genotype Probability for individual genotypes with missing data. If not, use an empirical approximation to impute the LGPs. Defaults to TRUE because the side plots in the extended GenePlot use the saddlepoint approximation process. |
leave_one_out |
(default TRUE) Boolean, indicates whether or not to calculate leave-one-out results for any individual from the reference pops. If TRUE, any individual from a reference population will have their Log-Genotype-Probability with respect to their own reference population after temporarily removing the individual's genotype from the sample data for that reference population. The individual's Log-Genotype-Probabilities with respect to all populations they are not a member of will be calculated as normal. We STRONGLY RECOMMEND using leave-one-out=TRUE for any small reference samples (<30). |
rel_tol |
(default NULL) Specify the relative tolerance for the
numerical integration function that is used to calculate the overlap area
and also the normalization constants for the various distributions. The
default value corresponds to the |
abs_tol |
(default NULL) Specify the absolute tolerance for the
numerical integration function that is used to calculate the overlap area
and also the normalization constants for the various distributions. The
default value corresponds to the |
npts |
(default 1000) Number of values to use when calculating numerical integrals (for the overlap area measures, and for the normalization constants of the distributions). Increasing this value will increase the precision of the numerical integrals but will also increase the computational cost. Reducing this below 1000 may save some computation time if you are not too concerned with the precision of the results. |
A list with the following components:
logprob
GenePlot calculation results: Log-Genotype Probability
values for all individuals with respect to all of the reference populations.
If there are individuals with missing values, their raw LGPs are shown
which are based on the loci that are present, and also the imputed LGPs
for the full set of loci. This output is the same as the output from
calc_logprob.
spdf_vals1
Saddlepoint distribution approximations with the first
reference population as the baseline. List contains xvals
,
yvals
, wvals
and zvals
, the raw distribution curves
for plotting the distributions.
This list also contains oavals
, probvals
and
diffvals
, which are the Overlap Area, Incumbent Selection
Probability and Home Assignment Probability values for the given baseline
population with all the other populations as comparisons. The sub-list
also records the quantile values requested, the name of the given baseline
pop for this sub-list as refpopA
, the indices of the baseline pop
and comparison pop in the reference pops, the name of the other reference
population and the number of other reference populations (always equal to
one).
spdf_vals2
As for spdf_vals1
, but with the second reference
population as the baseline.
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