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#' Create frequency matrix
#'
#' @usage createFrequencyMat(substrates.seq)
#'
#' @param substrates.seq A substrate sequence
#'
#' @return A frequency matrix of amino acid from substrates.seq.
#'
#' @examples
#'
#' data("phospho_L6_ratio")
#'
#' # We will create a frequency matrix of Tfg S198 phosphosite.
#' rownames(phospho.L6.ratio)[1]
#' substrate.seq = unlist(lapply(strsplit(rownames(phospho.L6.ratio)[1],
#' split = "~"), function(i) i[4]))
#' freq.mat = createFrequencyMat(substrate.seq)
#'
#' @export
createFrequencyMat <- function(substrates.seq) {
# substrates.seq.split <-
# sapply(substrates.seq, strsplit, '')
substrates.seq.split = mapply(strsplit,
substrates.seq, MoreArgs = list(split = ""))
frequency.mat <- matrix(data = 0, nrow = 20,
ncol = length(substrates.seq.split[[1]]))
rownames(frequency.mat) <- c("A", "R",
"N", "D", "C", "E", "Q", "G", "H",
"I", "L", "K", "M", "F", "P", "S",
"T", "W", "Y", "V")
colnames(frequency.mat) <- paste("p",
seq_len(length(substrates.seq.split[[1]])),
sep = "")
# calculate frequency
for (i in seq_len(ncol(frequency.mat))) {
# aa <- sapply(substrates.seq.split,
# function(x)x[i])
aa = mapply(function(x, i) x[i],
substrates.seq.split, MoreArgs = list(i = i))
for (j in seq_len(length(aa))) {
if (aa[j] == "_") {
next
}
frequency.mat[aa[j], i] <- frequency.mat[aa[j],
i] + 1
}
}
frequency.mat <- frequency.mat/length(substrates.seq)
return(frequency.mat)
}
#' Frequency scoring
#'
#' @usage frequencyScoring(sequence.list, frequency.mat)
#'
#' @param sequence.list A vector list of sequences
#' @param frequency.mat A matrix output from `createFrequencyMat`
#'
#' @return A vector of frequency score
#'
#' @examples
#'
#' data('phospho_L6_ratio')
#' data('KinaseMotifs')
#'
#' # Extracting first 10 sequences for demonstration purpose
#' seqs = unlist(lapply(strsplit(rownames(phospho.L6.ratio), "~"),
#' function(i) {i[4]}))
#' seqs = seqs[1:10]
#'
#' # extracting flanking sequences
#' seqWin = mapply(function(x) {
#' mid <- (nchar(x)+1)/2
#' substr(x, start=(mid-7), stop=(mid+7))
#' }, seqs)
#'
#' # The first 10 for demonstration purpose
#' phospho.L6.ratio = phospho.L6.ratio[1:10,]
#'
#' # minimum number of sequences used for compiling motif for each kinase.
#' numMotif=5
#'
#' motif.mouse.list.filtered <-
#' motif.mouse.list[which(motif.mouse.list$NumInputSeq >= numMotif)]
#'
#' # scoring all phosphosites against all motifs
#' motifScoreMatrix <-
#' matrix(NA, nrow=nrow(phospho.L6.ratio),
#' ncol=length(motif.mouse.list.filtered))
#' rownames(motifScoreMatrix) <- rownames(phospho.L6.ratio)
#' colnames(motifScoreMatrix) <- names(motif.mouse.list.filtered)
#'
#' # Scoring phosphosites against kinase motifs
#' for(i in seq_len(length(motif.mouse.list.filtered))) {
#' motifScoreMatrix[,i] <-
#' frequencyScoring(seqWin, motif.mouse.list.filtered[[i]])
#' cat(paste(i, '.', sep=''))
#' }
#'
#' @export
frequencyScoring <- function(sequence.list, frequency.mat) {
frequency.score <- c()
for (idx in seq_len(length(sequence.list))) {
if (sequence.list[idx] == "") {
sequence.list[idx] = "_"
}
# seqs <-
# unlist(sapply(sequence.list[idx],
# strsplit, ''))
seqs = unlist(mapply(strsplit, sequence.list[idx],
MoreArgs = list(split = "")))
score <- 0
if (is.na(sequence.list[idx])) {
frequency.score <- c(frequency.score,
score)
next
}
for (i in seq_len(length(seqs))) {
aa <- c("A", "R", "N", "D", "C",
"E", "Q", "G", "H", "I",
"L", "K", "M", "F", "P",
"S", "T", "W", "Y", "V")
if (!seqs[i] %in% aa) {
next
}
score <- frequency.mat[seqs[i],
i] + score
}
frequency.score <- c(frequency.score,
score)
}
if (!is.null(names(sequence.list))) {
names(frequency.score) <- names(sequence.list)
}
return(frequency.score)
}
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