freqdist.evaluate.core {EvaluateCore} | R Documentation |
Frequency Distribution Histogram
Description
Plot stacked frequency distribution histogram to graphically compare the probability distributions of traits between entire collection (EC) and core set (CS).
Usage
freqdist.evaluate.core(
data,
names,
quantitative,
qualitative,
selected,
highlight = NULL,
include.highlight = TRUE,
highlight.se = NULL,
highlight.col = "red"
)
Arguments
data |
The data as a data frame object. The data frame should possess one row per individual and columns with the individual names and multiple trait/character data. |
names |
Name of column with the individual names as a character string |
quantitative |
Name of columns with the quantitative traits as a character vector. |
qualitative |
Name of columns with the qualitative traits as a character vector. |
selected |
Character vector with the names of individuals selected in
core collection and present in the |
highlight |
Individual names to be highlighted as a character vector. |
include.highlight |
If |
highlight.se |
Optional data frame of standard errors for the
individuals specified in |
highlight.col |
The colour(s) to be used to highlighting individuals in
the plot as a character vector of the same length as |
Value
A list with the ggplot
objects of stacked frequency
distribution histograms plots for each trait specified as
quantitative
and qualitative
.
See Also
Examples
data("cassava_CC")
data("cassava_EC")
ec <- cbind(genotypes = rownames(cassava_EC), cassava_EC)
ec$genotypes <- as.character(ec$genotypes)
rownames(ec) <- NULL
core <- rownames(cassava_CC)
quant <- c("NMSR", "TTRN", "TFWSR", "TTRW", "TFWSS", "TTSW", "TTPW", "AVPW",
"ARSR", "SRDM")
qual <- c("CUAL", "LNGS", "PTLC", "DSTA", "LFRT", "LBTEF", "CBTR", "NMLB",
"ANGB", "CUAL9M", "LVC9M", "TNPR9M", "PL9M", "STRP", "STRC",
"PSTR")
ec[, qual] <- lapply(ec[, qual],
function(x) factor(as.factor(x)))
freqdist.evaluate.core(data = ec, names = "genotypes",
quantitative = quant, qualitative = qual,
selected = core)
checks <- c("TMe-1199", "TMe-1957", "TMe-3596", "TMe-3392")
freqdist.evaluate.core(data = ec, names = "genotypes",
quantitative = quant, qualitative = qual,
selected = core,
highlight = checks, highlight.col = "red")
quant.se <- data.frame(genotypes = checks,
NMSR = c(0.107, 0.099, 0.106, 0.062),
TTRN = c(0.081, 0.072, 0.057, 0.049),
TFWSR = c(0.089, 0.031, 0.092, 0.097),
TTRW = c(0.064, 0.031, 0.071, 0.071),
TFWSS = c(0.106, 0.071, 0.121, 0.066),
TTSW = c(0.084, 0.045, 0.066, 0.054),
TTPW = c(0.098, 0.052, 0.111, 0.082),
AVPW = c(0.074, 0.038, 0.054, 0.061),
ARSR = c(0.104, 0.019, 0.204, 0.044),
SRDM = c(0.078, 0.138, 0.076, 0.079))
freqdist.evaluate.core(data = ec, names = "genotypes",
quantitative = quant,
selected = core,
highlight = checks, highlight.col = "red",
highlight.se = quant.se)