218 lines
6.0 KiB
R
218 lines
6.0 KiB
R
# .utilities.R
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#
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# Miscellaneous R code to suppport the project
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#
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# Version: 1.3
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# Date: 2017 09 - 2017 10
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# Author: Boris Steipe
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#
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# V 1.3 load msa support functions
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# V 1.2 update database utilities to support 2017 version of JSON sources
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# V 1.1 2017 updates for ABC-units
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# V 1.0 First code
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#
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# ToDo:
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# Notes:
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#
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# ==============================================================================
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# ====== SCRIPTS =============================================================
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source("./scripts/ABC-dbUtilities.R")
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source("./scripts/ABC-writeALN.R")
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source("./scripts/ABC-writeMFA.R")
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# ====== SUPPORT FUNCTIONS =====================================================
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objectInfo <- function(x) {
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# Function to combine various information items about R objects
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#
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# Input: an R object
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# Value: none - prints information as side-effect
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cat("object contents:")
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print(x, digits = 22) # print value at maximal precision
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cat("\nstructure of object:\n")
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str(x)
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if (! is.list(x)) { # Don't use cat() if x is a list. cat() can't handle lists.
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cat("\nmode: ", mode(x), "\n")
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cat("typeof: ", typeof(x), "\n")
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cat("class: ", class(x), "\n")
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}
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# if the object has attributes, print them too
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if (! is.null(attributes(x))) {
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cat("\nattributes:\n")
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attributes(x)
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}
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# Done
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}
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biCode <- function(s) {
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# Make a 5 character "biCode" from a binomial name by concatening
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# the uppercased first three letter of the first word and the first
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# two letters of the second word. If there is only one word, we take the
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# first five characters from that. Outputs are padded with "." if necessary.
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# NAs in input are preserved.
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# Parameters:
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# s chr vector of binomial species names
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# Value: chr vector of biCodes, same length as s, NAs are preserved
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b <- character(length(s))
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s <- gsub("[^a-zA-Z ]", "", as.character(s)) # remove all non-alphabetic
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# characters except space
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s <- toupper(s)
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for (i in seq_along(s)) {
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x <- unlist(strsplit(s[i], "\\s+"))
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if (length(x) == 0) { # empty string
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x <- c("", "")
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} else if (length(x) == 1) { # only one string
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x <- c(substr(x, 1, 3), substr(x, 4, 5)) # 3 + 2 with whatever is there
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}
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x <- paste0(x[1:2], "...") # pad strings
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b[i] <- paste0(substr(x[1], 1, 3), substr(x[2], 1, 2))
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}
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b[is.na(s)] <- NA # recover NAs from input
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return(b)
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}
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pBar <- function(i, l, nCh = 50) {
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# Draw a progress bar in the console
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# i: the current iteration
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# l: the total number of iterations
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# nCh: width of the progress bar
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ticks <- round(seq(1, l-1, length.out = nCh))
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if (i < l) {
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if (any(i == ticks)) {
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p <- which(i == ticks)
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p1 <- paste(rep("#", p), collapse = "")
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p2 <- paste(rep("-", nCh - p), collapse = "")
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cat(sprintf("\r|%s%s|", p1, p2))
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flush.console()
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}
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}
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else { # done
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cat("\n")
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}
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}
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waitTimer <- function(t, nIntervals = 50) {
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# pause and wait for t seconds and display a progress bar as
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# you are waiting
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t <- as.numeric(t)
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if (t < 0.1) {return(invisible())}
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increment <- t / nIntervals
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bar <- "----:----|" # One module for the progress bar:
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bar <- rep(bar, ceiling(nIntervals / 10)) # repeat,
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bar <- unlist(strsplit(bar, "")) # split into single characters,
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bar <- bar[1:nIntervals] # truncate,
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bar <- paste(bar, collapse="") # and collapse.
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cat(sprintf("\nWaiting: |%s\n |", bar))
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for (i in 1:(nIntervals - 1)) {
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Sys.sleep(increment)
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cat("=")
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}
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Sys.sleep(increment)
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cat("|\n\n")
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return(invisible())
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}
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fetchMSAmotif <- function(ali, mot) {
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# retrieve a subset from ali that spans the sequence in mot.
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# Parameters:
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# ali MsaAAMultipleAlignment object
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# mot chr substring within ali
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# Value: AAStringset
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if (class(ali) != "MsaAAMultipleAlignment" &&
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class(ali) != "MsaDNAMultipleAlignment" &&
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class(ali) != "MsaRNAMultipleAlignment") {
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stop("ali has to be an msa multiple alignment object.")
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}
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if (class(mot) != "character") {
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stop("mot has to be a character object.")
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}
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x <- gsub("-", "", as.character(ali)) # pure sequence, no hyphens
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idx <- grep(mot, x)[1] # first sequence containing mot. If no match,
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# idx becomes NA
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if (is.na(idx)) {
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stop("mot is not a subsequence in ali.")
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}
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# Find the match range
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m <- regexpr(mot, x[idx])
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motifStart <- as.numeric(m)
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motifEnd <- attr(m, "match.length") + motifStart - 1
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# Count characters, skip hyphens ...
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x <- unlist(strsplit(as.character(ali)[idx], ""))
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x <- x != "-"
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x <- as.numeric(x)
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x <- cumsum(x)
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return(subseq(ali@unmasked,
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start = which(x == motifStart)[1], # get the first position
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end = which(x == motifEnd)[1]))
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}
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# ====== PDB ID selection ======================================================
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selectPDBrep <- function(n) {
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# Select n PDB IDs from a list of high-resolution, non-homologous, single
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# domain, single chain structure files that represent a CATH topology
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# group.
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# Parameters n num number of IDs to return.
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# Value: char PDB IDs
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# Note: the list is loaded from an RData file in the data directory
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load("./data/pdbRep.RData") # loads pdbRep
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if (n > length(pdbRep)) {
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stop(sprintf("You can select no more than %d IDs.", length(pdbRep)))
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}
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set.seed(as.numeric(Sys.time()))
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return(sample(pdbRep, n))
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}
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# ====== DATA ==================================================================
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# 10 species of fungi for reference analysis.
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# http://steipe.biochemistry.utoronto.ca/abc/index.php/Reference_species_for_fungi
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REFspecies <- c("Aspergillus nidulans",
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"Bipolaris oryzae",
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"Coprinopsis cinerea",
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"Cryptococcus neoformans",
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"Neurospora crassa",
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"Puccinia graminis",
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"Saccharomyces cerevisiae",
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"Schizosaccharomyces pombe",
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"Ustilago maydis",
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"Wallemia mellicola"
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)
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# [END]
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