Nothing
###############################################################################
# Function to get the vector of sequences for the crossover designs
#
# Author: dlabes
###############################################################################
sequences <- function(design, tmts=NULL)
{
seqs <- character()
ntmt <- 2
if(design!="parallel") ntmt <- as.numeric(substr(design,1,1))
if (!is.null(tmts) & length(tmts)!=ntmt){
stop ("Treatment codes must have ", ntmt, " entries!")
}
# classical 2x2 crossover
if(design=="2x2" | design=="2x2x2") seqs <- c("AB","BA")
# 2-group parallel
if(design=="parallel") seqs <- c("A","B")
# 3x3 crossover
if(design=="3x3" | design=="3x3x3"){
seqs <- c("ABC","BCA","CAB")
# randomize it
seqs <- randLS(seqs)
}
# 3x3 crossover: Williams design with 6 sequencess
if(design=="3x6x3"){
seqs <- c("ABC",
"BCA",
"CAB",
"ACB",
"BAC",
"CBA")
}
# 4x4 crossover
if(design=="4x4" | design=="4x4x4"){
# this is one of the four standard latin squares, it is a williams design
seqs <- c("ABCD",
"BDAC",
"CADB",
"DCBA")
# eventually we should randomize it? yes
seqs <- randLS(seqs)
# although the standard Latin square is a williams design
# the randLS gives not always a Williams design back
}
# partial replicate (reference replicate)
if(design=="2x3x3") seqs <- c("ABB","BAB","BBA")
# 2-sequence-3-period full replicate
if(design=="2x2x3") seqs <- c("ABA","BAB")
# 2-sequence-4-period full replicate: FDA design
if(design=="2x2x4") seqs <- c("ABAB","BABA")
# 4-sequence-4-period full replicate
# Chen, Chow, Li: "SAMPLE SIZE higher order crossover"
if(design=="2x4x4") seqs <- c("ABBA","BAAB","AABB","BBAA")
# Baalams design
if(design=="2x4x2") seqs <- c("AB","BA","AA","BB")
# if tmts are given
if (! is.null(tmts)){
#replace the a codes by tmts
for (i in seq_along(tmts)){
st <- LETTERS[i]
seqs <- gsub(st,tmts[i],seqs)
}
}
if (length(seqs)==0) stop("Design not implemented!")
return(seqs)
}
# ------------------------------------------------------------------------
# internal function to randomize latin square
randLS <- function(seqs)
{
seqm <- strsplit(seqs, split="")
n <- length(seqm)
seqm2 <- matrix(nrow=n,ncol=n)
for (i in seq_along(seqm)){
seqm2[i,] <- seqm[[i]]
}
rows <- sample(1:n)
cols <- sample(1:n)
# order by rows
seqm2 <- seqm2[rows,]
seqm2 <- seqm2[,cols]
# sort by first col?
seqm2 <- seqm2[order(seqm2[,1]),]
for (i in seq_along(seqm2[,1])){
seqs[i] <- paste(seqm2[i,],sep="",collapse="")
}
seqs
}
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