View source: R/cr.evaluate.core.R
cr.evaluate.core | R Documentation |
Compute the Coincidence Rate of Range (\mjseqnCR) \insertCitehu_methods_2000EvaluateCore (originally described by \insertCitediwan_methods_1995EvaluateCore as Mean range ratio) to compare quantitative traits of the entire collection (EC) and core set (CS). \loadmathjax
cr.evaluate.core(data, names, quantitative, selected)
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. |
selected |
Character vector with the names of individuals selected in
core collection and present in the |
The Coincidence Rate of Range (\mjseqnCR) is computed as follows.
\mjsdeqnCR = \left ( \frac1n \sum_i=1^n \fracR_CS_iR_EC_i \right ) \times 100
Where, \mjseqnR_CS_i is the range of the \mjseqnith trait in the CS, \mjseqnR_EC_i is the range of the \mjseqnith trait in the EC and \mjseqnn is the total number of traits.
A representative CS should have a \mjseqnCR value no less than 70% \insertCitediwan_methods_1995EvaluateCore or 80% \insertCitehu_methods_2000EvaluateCore.
The \mjseqnCR value.
wilcox.test
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))) cr.evaluate.core(data = ec, names = "genotypes", quantitative = quant, selected = core)
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