#' @title compareCodons
#' @name compareCodons
#' @description This function compares two codons and returns the number of syn
#'and non-syn sites according to \emph{Nei and Gojobori (1986)}.
#' @param codA \code{codon} A [mandatory]
#' @param codB \code{codon} B [mandatory]
#' @return vector of syn and non-syn sites
#' @importFrom Biostrings DNAString DNAStringSet AAString AAStringSet
#' readDNAStringSet readAAStringSet writeXStringSet width subseq
#' pairwiseAlignment
#' @importFrom seqinr kaks
#' @seealso \code{\link[seqinr]{kaks}}
#' @references Nei and Gojobori. (1986) Simple methods for estimating the
#' numbers of synonymous and nonsynonymous nucleotide substitutions.
#' \emph{Mol. Biol. Evol.}, \bold{3(5)}, 418-426.
#' @references Ganeshan et al. (1997) Human immunodeficiency virus type 1
#' genetic evolution in children with different rates of development of disease.
#' \emph{J. Virology.} \bold{71(1)}, 663-677.
#' @references Yang et al. (2000) Codon-substitution models for heterogeneous
#' selection pressure at amino acid sites. \emph{Genetics.}
#' \bold{155(1)}, 431-449.
#' @examples
#' compareCodons("AAA","TTA")
#' compareCodons("AAA","TAT")
#' compareCodons("AAA","ATT")
#' compareCodons("AAA","TTT")
#' ## load example sequence data
#' data("hiv", package="distSTRING")
#' compareCodons(dnastring2codonmat(hiv)[1,1], dnastring2codonmat(hiv)[1,2])
#' @export compareCodons
#' @author Kristian K Ullrich
compareCodons <- function(codA, codB){
type <- "syn"
if(codA == codB){
return(c(0, 0, 0))
}
codAsplit <- strsplit(codA, "")[[1]]
codBsplit <- strsplit(codB, "")[[1]]
if("N" %in% codAsplit | "N" %in% codBsplit){
type <- "Ns"
return(c(NA, NA, NA))
}
if("-" %in% codAsplit | "-" %in% codBsplit){
type <- "indel"
return(c(0, 0, 1))
}
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] !=
distSTRING::GENETIC_CODE_TCAG[codB, 2]){
type <- "nonsyn"
}
codAcodB_diff_idx <- which(codAsplit != codBsplit)
if(length(codAcodB_diff_idx) == 1){
if(type == "syn"){
return(c(1, 0, 0))
}
if(type == "nonsyn"){
return(c(0, 1, 0))
}
}
if(length(codAcodB_diff_idx) == 2){
## AAA (Lys) -> TTA (Leu)
## AGC (Ser) -> TCC (Ser)
if(all(codAcodB_diff_idx == c(1, 2))){
codC <- paste0(codBsplit[1], codAsplit[2], codAsplit[3])
codD <- paste0(codAsplit[1], codBsplit[2], codAsplit[3])
}
## AAA -> TAT
if(all(codAcodB_diff_idx == c(1, 3))){
codC <- paste0(codBsplit[1], codAsplit[2], codAsplit[3])
codD <- paste0(codAsplit[1], codAsplit[2], codBsplit[3])
}
## AAA -> ATT
if(all(codAcodB_diff_idx == c(2, 3))){
codC <- paste0(codAsplit[1], codBsplit[2], codAsplit[3])
codD <- paste0(codAsplit[1], codAsplit[2], codBsplit[3])
}
tmp_syn <- 0
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] ==
distSTRING::GENETIC_CODE_TCAG[codC, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] ==
distSTRING::GENETIC_CODE_TCAG[codD, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codB, 2] ==
distSTRING::GENETIC_CODE_TCAG[codC, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codB, 2] ==
distSTRING::GENETIC_CODE_TCAG[codD, 2]){
tmp_syn <- tmp_syn + 1
}
tmp_syn <- tmp_syn / 2
return(c(tmp_syn, 2 - tmp_syn, 0))
}
if(length(codAcodB_diff_idx) == 3){
## AAA -> TTT
codC <- paste0(codBsplit[1], codAsplit[2], codAsplit[3])
codD <- paste0(codAsplit[1], codBsplit[2], codAsplit[3])
codE <- paste0(codAsplit[1], codAsplit[2], codBsplit[3])
codF <- paste0(codBsplit[1], codBsplit[2], codAsplit[3])
codG <- paste0(codBsplit[1], codAsplit[2], codBsplit[3])
codH <- paste0(codAsplit[1], codBsplit[2], codBsplit[3])
tmp_syn <- 0
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] ==
distSTRING::GENETIC_CODE_TCAG[codC, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] ==
distSTRING::GENETIC_CODE_TCAG[codD, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codA, 2] ==
distSTRING::GENETIC_CODE_TCAG[codE, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codB, 2] ==
distSTRING::GENETIC_CODE_TCAG[codF, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codB, 2] ==
distSTRING::GENETIC_CODE_TCAG[codG, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codB, 2] ==
distSTRING::GENETIC_CODE_TCAG[codH, 2]){
tmp_syn <- tmp_syn + 1
}
if(distSTRING::GENETIC_CODE_TCAG[codC, 2] ==
distSTRING::GENETIC_CODE_TCAG[codF, 2]){
tmp_syn <- tmp_syn + 0.5
}
if(distSTRING::GENETIC_CODE_TCAG[codC, 2] ==
distSTRING::GENETIC_CODE_TCAG[codG, 2]){
tmp_syn <- tmp_syn + 0.5
}
if(distSTRING::GENETIC_CODE_TCAG[codD, 2] ==
distSTRING::GENETIC_CODE_TCAG[codF, 2]){
tmp_syn <- tmp_syn + 0.5
}
if(distSTRING::GENETIC_CODE_TCAG[codD, 2] ==
distSTRING::GENETIC_CODE_TCAG[codH, 2]){
tmp_syn <- tmp_syn + 0.5
}
if(distSTRING::GENETIC_CODE_TCAG[codE, 2] ==
distSTRING::GENETIC_CODE_TCAG[codG, 2]){
tmp_syn <- tmp_syn + 0.5
}
if(distSTRING::GENETIC_CODE_TCAG[codE, 2] ==
distSTRING::GENETIC_CODE_TCAG[codH, 2]){
tmp_syn <- tmp_syn + 0.5
}
tmp_syn <- tmp_syn / 3
return(c(tmp_syn, 3 - tmp_syn, 0))
}
}
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