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##' calculate difference of two aligned sequences
##'
##'
##' @title seqdiff
##' @param fasta fasta file
##' @param reference which sequence serve as reference, 1 or 2
##' @return SeqDiff object
##' @export
##' @importFrom Biostrings readBStringSet
##' @importClassesFrom Biostrings BStringSet
##' @importFrom methods new
##' @author guangchuang yu
##' @examples
##' fas <- list.files(system.file("examples","GVariation", package="seqcombo"), pattern="fas", full.names=TRUE)
##' seqdiff(fas[1], reference=1)
seqdiff <- function(fasta, reference=1) {
sequence <- readBStringSet(fasta)
if (length(sequence) != 2 && length(width(sequence)) != 1) {
stop("fas should contains 2 aligned sequences...")
}
diff <- nucleotide_difference(sequence, reference)
new("SeqDiff",
file = fasta,
sequence = sequence,
reference = reference,
diff = diff)
}
##' @importFrom magrittr %>%
##' @importFrom Biostrings toString
##' @importFrom Biostrings width
nucleotide_difference <- function(x, reference=1) {
n <- width(x[1])
nn <- seq_len(n)
s1 <- x[1] %>% toString %>% substring(nn, nn)
s2 <- x[2] %>% toString %>% substring(nn, nn)
pos <- which(s1 != s2)
if (reference == 1) {
diff <- s2[pos]
} else {
diff <- s1[pos]
}
return(data.frame(position = pos,
difference = diff,
stringsAsFactors = FALSE))
}
##' @importFrom dplyr group_by
##' @importFrom dplyr summarize
##' @importFrom dplyr select
##' @importFrom dplyr n
nucleotide_difference_count <- function(x, width=50, keep0=FALSE) {
n <- max(x$position)
bin <- rep(1:ceiling(n/width), each=width)
position <- c(seq_len(n)[!duplicated(bin)], n)
x$bin <- bin[x$pos]
y <- x %>% group_by(bin) %>%
summarize(position=min(position), count = n()) %>%
select(-bin)
y$position <- position[findInterval(y$position, position)]
if (keep0) {
itv <- seq(1, n, width)
yy <- data.frame(position = itv[!itv %in% y$position],
count = 0)
y <- rbind(y, yy)
y <- y[order(y$position, decreasing=FALSE),]
}
return(y)
}
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