Nothing
stats.coord <-
function(ind, loci, alpha) {
# Descr: generate significance tables
# Deps: stats.outmaker
# I/p: ind
# loci
# alpha
# Note: CV = coefficient of variance
# avgs = arithmetic means
# qntls = quantiles
debugBool = get("P2C2M_flg_dbgBool", envir=P2C2M_globalVars)
slctn = get("P2C2M_flg_dscrStat", envir=P2C2M_globalVars)
if (debugBool) {
cat("\n", xtermStyle::style("DEBUG> stats.coord", fg="red"), "\n",
sep="")
}
##############################
# 1. Setting number of tails #
##############################
# T-tests for all descriptive statistics are two-tailed, because there is no
# a priori reason in which direction they should differ.
tailL = list()
tailL$LCWT = "2"
tailL$COAL = "2"
tailL$NDC = "2"
tailL$GSI = "2"
## T-tests for NDC should be left one-tailed, because trees not compliant
## with the coalescent model have a higher number of deep coalescences.
#NDCtail = "1l"
## T-tests for GSI should be right one-tailed, because trees not compliant
## with the coalescent model have lower values.
#GSItail = "1r"
#############################
# 2. Inferring significance #
#############################
perGene = acrGenes = list()
for (s in slctn) {
perGene[[s]] = stats.perGene(ind[[s]]$dif, alpha, tailL[[s]])
acrGenes[[s]] = stats.acrGenes(ind[[s]]$dif, alpha, tailL[[s]])
}
#######################
# 3. Combining output #
#######################
outList = list()
# perGene output
outList$perGene = sapply(perGene, cbind)
rownames(outList$perGene) = c(loci)
# acrossGene output
outList$acrGenes = sapply(acrGenes, cbind)
rownames(outList$acrGenes) = c("Sum", "Mean", "Median", "Mode", "CV")
# Naming rows of output
names = c()
for (stat in slctn) {
names = c(names, paste(stat, "[", tailL[[stat]], "]", sep=""))
}
colnames(outList$perGene) = colnames(outList$acrGenes) = names
return(outList)
}
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