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#' Translate nucleic acid sequences into codons
#'
#' The function transforms \code{dna2codon} DNA sequences to codon sequences,
#' \code{codon2dna} transform the other way. \code{dna2codon} translates
#' nucleotide to amino acids using the function \code{\link[ape]{trans}}.
#'
#' The following genetic codes are described here. The number preceding each
#' corresponds to the code argument.
#' \tabular{rl}{
#' 1 \tab standard \cr
#' 2 \tab vertebrate.mitochondrial \cr
#' 3 \tab yeast.mitochondrial \cr
#' 4 \tab protozoan.mitochondrial+mycoplasma \cr
#' 5 \tab invertebrate.mitochondrial \cr
#' 6 \tab ciliate+dasycladaceal \cr
#' 9 \tab echinoderm+flatworm.mitochondrial \cr
#' 10 \tab euplotid \cr
#' 11 \tab bacterial+plantplastid \cr
#' 12 \tab alternativeyeast \cr
#' 13 \tab ascidian.mitochondrial \cr
#' 14 \tab alternativeflatworm.mitochondrial \cr
#' 15 \tab blepharism \cr
#' 16 \tab chlorophycean.mitochondrial \cr
#' 21 \tab trematode.mitochondrial \cr
#' 22 \tab scenedesmus.mitochondrial \cr
#' 23 \tab thraustochytrium.mitochondria \cr
#' 24 \tab Pterobranchia.mitochondrial \cr
#' 25 \tab CandidateDivision.SR1+Gracilibacteria \cr
#' 26 \tab Pachysolen.tannophilus
#' }
#' Alignment gaps and ambiguities are currently ignored and sites containing
#' these are deleted.
#'
#' @aliases
#' dna2codon codon2dna
#' @param x An object containing sequences.
#' @param codonstart an integer giving where to start the translation. This
#' should be 1, 2, or 3, but larger values are accepted and have for effect to
#' start the translation further within the sequence.
#' @param code The ncbi genetic code number for translation (see details).
#' By default the standard genetic code is used.
#' @param ambiguity character for ambiguous character and no contrast is
#' provided.
#' @param ... further arguments passed to or from other methods.
#' @return The functions return an object of class \code{phyDat}.
#' @author Klaus Schliep \email{klaus.schliep@@gmail.com}
#' @references \url{https://www.ncbi.nlm.nih.gov/Taxonomy/taxonomyhome.html/index.cgi?chapter=cgencodes}
#' @seealso \code{\link[ape]{trans}}, \code{\link{phyDat}} and the chapter 4 in
#' the \code{vignette("phangorn-specials", package="phangorn")}
#' @keywords cluster
#' @examples
#'
#' data(Laurasiatherian)
#' class(Laurasiatherian)
#' Laurasiatherian
#' dna2codon(Laurasiatherian)
#'
#' @rdname dna2codon
#' @export
dna2codon <- function(x, codonstart=1, code=1, ambiguity="---", ...){
if(!inherits(x, "phyDat"))stop("x must be of class phyDat")
if(attr(x, "type")!="DNA")stop("x must be a nucleotide sequence!")
if(codonstart>1){
del <- -seq_len(codonstart)
x <- subset(x, select=del, site.pattern=FALSE)
}
n_sites <- sum(attr(x, "weight"))
if( (n_sites %% 3) ){
keep <- seq_len( (n_sites %/% 3) * 3 )
x <- subset(x, select=keep, site.pattern=FALSE)
}
phyDat.codon(as.character(x), ambiguity=ambiguity, code=code, ...)
}
#' @rdname dna2codon
#' @export
codon2dna <- function(x){
stopifnot(inherits(x, "phyDat"))
phyDat.DNA(as.character(x))
}
#' @rdname dna2codon
#' @export
dna2aa <- function(x, codonstart=1, code=1){
stopifnot(inherits(x, "phyDat"))
if(attr(x, "type")!="DNA")stop("x must be a nucleotide sequence!")
dna <- as.DNAbin(x)
aa <- as.phyDat(trans(dna, code=code, codonstart=codonstart))
}
synonymous_subs <- function(code=1, stop.codon=FALSE){
tmp <- .CODON[, as.character(code)]
label <- rownames(.CODON)
l <- length(tmp)
res <- matrix(1, 64, 64, dimnames = list(label, label))
for(i in seq_len(64)){
for(j in seq_len(64)) {
if(tmp[i] == tmp[j]) res[i, j] <- 0
}
}
res[.ONE_TRANSITION == FALSE] <- -1
if(!stop.codon){
label <- label[tmp != "*"]
res <- res[label, label]
}
res[lower.tri(res)]
}
tstv_subs <- function(code=1, stop.codon=FALSE){
tmp <- .CODON[, as.character(code)]
label <- rownames(.CODON)
res <- .SUB
if(!stop.codon){
label <- label[tmp != "*"]
res <- res[label, label]
}
res[lower.tri(res)]
}
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