`map.det.lme` <-
function(input, s.chr, chrSet, prevLoc=NULL)
{
dfMerged <- input$dfMerged
fixed <- input$envModel$fixed
n.chr <- length(input$map)
nphe <- input$nphe
type <- attr(input, "type")
results <- list()
formula <- list()
chrRE <- vector()
wald <- rep(0, length(input$map[[s.chr]]))
# Set up random effects for markers on each chromosome
for (kk in 1:n.chr)
chrRE[kk] <- paste("pdIdent(~", paste(setdiff(names(dfMerged)[grep(paste("C", kk, "M", sep=""), names(dfMerged))], prevLoc), collapse="+"), "-1)", sep="")
# Loop over positions on the selected chromosome
mrkloop <- unlist(lapply(strsplit(names(dfMerged)[setdiff(grep(paste("C", s.chr, "M", sep=""), names(dfMerged)[(nphe+1):ncol(dfMerged)]), match(prevLoc, colnames(dfMerged)[(nphe+1):ncol(dfMerged)]))+nphe], "M"), function(x) return(x[2])))
if (type=="f2")
mrkloop <- unique(substr(mrkloop, 1, nchar(mrkloop)-1))
mrkloop <- as.numeric(mrkloop)
for (jj in 1:length(mrkloop))
{
# Only include random effects for chromosomes not being scanned
if (length(chrSet)>2)
formula$random <- paste("pdBlocked(list(", paste(chrRE[setdiff(chrSet, s.chr)], collapse=","), "))", sep="")
if (length(chrSet)==2)
formula$random <- chrRE[setdiff(chrSet,s.chr)]
formula$fixed <- paste(as.character(fixed)[2], "~", as.character(fixed)[3], sep="")
# If there are markers already mapped on other chromosomes, add in as fixed effects
if (length(prevLoc) >0)
formula$fixed <- paste(formula$fixed, "+",paste(prevLoc, collapse="+"), sep="")
effectnames <- paste("C", s.chr, "M", mrkloop[jj], sep="")
if (type=="f2") effectnames <- paste(effectnames, c("A", "D"), sep="")
formula$fixed <- paste(formula$fixed, "+", paste(effectnames, collapse="+"), sep="")
formula$fixgrp <- paste(formula$fixed, "| grp1", sep="")
formula$fixed <- as.formula(formula$fixed)
formula$fixgrp <- as.formula(formula$fixgrp)
gd <- groupedData(formula$fixgrp, data=dfMerged)
# Fit model - different forms depending on relevant terms
if (length(chrSet)>1)
model <- lme(fixed=formula$fixed, random=eval(parse(text=formula$random)), data=gd, control=lmeControl(maxIter=input$maxit), na.action=na.omit)
if (length(chrSet)==1)
model <- lme(fixed=formula$fixed, random=~1|grp1, data=gd, control=lmeControl(maxIter=input$maxit), na.action=na.omit)
# Get output - Wald statistic for position fixed effect
wald[jj] <- anova(model, Terms=effectnames)[1,3]
}
results$wald <- wald
return(results)
}
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