View source: R/freqdist.evaluate.core.R
freqdist.evaluate.core | R Documentation |
Plot stacked frequency distribution histogram to graphically compare the probability distributions of traits between entire collection (EC) and core set (CS).
freqdist.evaluate.core( data, names, quantitative, qualitative, selected, highlight = NULL, include.highlight = TRUE, highlight.se = NULL, highlight.col = "red" )
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 |
A list with the ggplot
objects of stacked frequency
distribution histograms plots for each trait specified as
quantitative
and qualitative
.
hist
, geom_histogram
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)
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