view get_length_and_gc_content.r @ 0:2ca1baabdae0 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/length_and_gc_content commit b7dcd020c6a15fa55f392cc09cbc37580d6e75c4
author iuc
date Thu, 17 Nov 2016 16:41:06 -0500
parents
children f088370d2a3c
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# originally by Devon Ryan, https://www.biostars.org/p/84467/

options( show.error.messages=F, error = function () { cat( geterrmessage(), file=stderr() ); q( "no", 1, F ) } )

# we need that to not crash galaxy with an UTF8 error on German LC settings.
loc <- Sys.setlocale("LC_MESSAGES", "en_US.UTF-8")

suppressPackageStartupMessages({
    library("GenomicRanges")
    library("rtracklayer")
    library("Rsamtools")
    library("optparse")
    library("data.table")
})

option_list <- list(
    make_option(c("-g","--gtf"), type="character", help="Input GTF file with gene / exon information."),
    make_option(c("-f","--fasta"), type="character", default=FALSE, help="Fasta file that corresponds to the supplied GTF."),
    make_option(c("-l","--length"), type="character", default=FALSE, help="Output file with gene name and length."),
    make_option(c("-gc","--gc_content"), type="character", default=FALSE, help="Output file with gene name and GC content.")
  )

parser <- OptionParser(usage = "%prog [options] file", option_list=option_list)
args = parse_args(parser)

GTFfile = args$gtf
FASTAfile = args$fasta
length = args$length
gc_content = args$gc_content

#Load the annotation and reduce it
GTF <- import.gff(GTFfile, format="gtf", genome=NA, feature.type="exon")
grl <- reduce(split(GTF, elementMetadata(GTF)$gene_id))
reducedGTF <- unlist(grl, use.names=T)
elementMetadata(reducedGTF)$gene_id <- rep(names(grl), elementNROWS(grl))

#Open the fasta file
FASTA <- FaFile(FASTAfile)
open(FASTA)

#Add the GC numbers
elementMetadata(reducedGTF)$nGCs <- letterFrequency(getSeq(FASTA, reducedGTF), "GC")[,1]
elementMetadata(reducedGTF)$widths <- width(reducedGTF)

#Create a list of the ensembl_id/GC/length
calc_GC_length <- function(x) {
    nGCs = sum(elementMetadata(x)$nGCs)
    width = sum(elementMetadata(x)$widths)
    c(width, nGCs/width)
}
output <- t(sapply(split(reducedGTF, elementMetadata(reducedGTF)$gene_id), calc_GC_length))
output <- data.frame(setDT(data.frame(output), keep.rownames = TRUE)[])


write.table(output[,c(1,2)], file=length, col.names=FALSE, row.names=FALSE, quote=FALSE, sep="\t")
write.table(output[,c(1,3)], file=gc_content, col.names=FALSE, row.names=FALSE, quote=FALSE, sep="\t")


sessionInfo()