diff gtf2featureAnnotation.R @ 7:14b3f2a4523b draft default tip

"planemo upload for repository https://github.com/ebi-gene-expression-group/container-galaxy-sc-tertiary/tree/develop/tools/gtf-2-gene-list/.shed.yml commit 5a62f18c80ddd55cfcc9d64546fde4e20be3e070"
author ebi-gxa
date Mon, 19 Jul 2021 08:00:24 +0000
parents 1a642de6db01
children
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line diff
--- a/gtf2featureAnnotation.R	Wed Mar 04 06:44:32 2020 -0500
+++ /dev/null	Thu Jan 01 00:00:00 1970 +0000
@@ -1,196 +0,0 @@
-#!/usr/bin/env Rscript
-
-# This script parses the GTF file to create a feature-wise annotation file with
-# mitochondrial features flagged, to assist in annotation and QC of single-cell
-# expression data analysis.
-
-suppressPackageStartupMessages(require(rtracklayer))
-suppressPackageStartupMessages(require(optparse))
-
-ucfirst <- function (str) {
-  paste(toupper(substring(str, 1, 1)), tolower(substring(str, 2)), sep = "")
-}
-
-die <- function(message){
-  write(message, stderr())
-  q(status = 1)
-}
-
-cleanlist <- function(str){
-  tolower(unlist(strsplit(str, ',')))
-}
-
-cl <- commandArgs(trailingOnly = TRUE)
-
-option_list = list(
-  make_option(
-    c("-g", "--gtf-file"),
-    action = "store",
-    default = NA,
-    type = 'character',
-    help = "Path to a valid GTF file"
-  ),
-  make_option(
-    c("-t", "--feature-type"),
-    action = "store",
-    default = 'gene',
-    type = 'character',
-    help = 'Feature type to use (default: gene)'
-  ),
-  make_option(
-    c("-f", "--first-field"),
-    action = "store",
-    default = 'gene_id',
-    type = 'character',
-    help = 'Field to place first in output table (default: gene_id)'
-  ),
-  make_option(
-    c("-r", "--no-header"),
-    action = "store_false",
-    default = TRUE,
-    type = 'logical',
-    help = 'Suppress header on output'
-  ),
-  make_option(
-    c("-l", "--fields"),
-    action = "store",
-    default = NULL,
-    type = 'character',
-    help = 'Comma-separated list of output fields to retain (default: all)'
-  ),
-  make_option(
-    c("-m", "--mito"),
-    action = "store_true",
-    default = FALSE,
-    type = 'character',
-    help = 'Mark mitochondrial elements with reference to chromsomes and biotypes'
-  ),
-  make_option(
-    c("-n", "--mito-chr"),
-    action = "store",
-    default = 'mt,mitochondrion_genome,mito,m,chrM,chrMt',
-    type = 'character',
-    help = 'If specified, marks in a column called "mito" features on the specified chromosomes (case insensitive)'
-  ),
-  make_option(
-    c("-p", "--mito-biotypes"),
-    action = "store",
-    default = 'mt_trna,mt_rrna,mt_trna_pseudogene',
-    type = 'character',
-    help = 'If specified,  marks in a column called "mito" features with the specified biotypes (case insensitve)'
-  ),
-  make_option(
-    c("-c", "--filter-cdnas"),
-    action = "store",
-    default = NULL,
-    type = 'character',
-    help = 'If specified, sequences in the provided FASTA-format cDNAs file will be filtered to remove entries not present in the annotation'
-  ),
-  make_option(
-    c("-d", "--filter-cdnas-field"),
-    action = "store",
-    default = 'transcript_id',
-    type = 'character',
-    help = 'Where --filter-cdnas is specified, what field should be used to compare to identfiers from the FASTA?'
-  ),
-  make_option(
-    c("-e", "--filter-cdnas-output"),
-    action = "store",
-    default = 'filtered.fa.gz',
-    type = 'character',
-    help = 'Where --filter-cdnas is specified, what file should the filtered sequences be output to?'
-  ),
-  make_option(
-    c("-u", "--version-transcripts"),
-    action = "store_true",
-    default = FALSE,
-    type = 'logical',
-    help = 'Where the GTF contains transcript versions, should these be appended to transcript identifiers? Useful when generating transcript/gene mappings for use with transcriptomes.'
-  ),
-  make_option(
-    c("-o", "--output-file"),
-    action = "store",
-    default = NA,
-    type = 'character',
-    help = 'Output file path'
-  )
-)
-
-opt <- parse_args(OptionParser(option_list = option_list), convert_hyphens_to_underscores = TRUE)
-
-if (is.na(opt$gtf_file)){
-  die('ERROR: No input GTF file specified')
-}
-
-if (is.na(opt$output_file)){
-  die('ERROR: No output file specified')
-}
-
-# Import the GTF
-
-print(paste('Reading', opt$gtf_file, 'elements of type', opt$feature_type))
-gtf <- import(opt$gtf_file, feature.type = opt$feature_type )
-
-# Combine basic info (chromosomes, coordinates) with annotation found in GTF attributes
-
-anno <- cbind(chromosome = seqnames(gtf), as.data.frame(ranges(gtf)), elementMetadata(gtf))
-print(paste('Found', nrow(anno), 'features'))
-
-# Mark mitochondrial features
-
-if (opt$mito){
-  anno$mito <- ucfirst(as.character(tolower(anno$gene_biotype) %in% cleanlist(opt$mito_biotypes) | tolower(anno$chromosome) %in% cleanlist(opt$mito_chr)))
-}
-
-# If specified, put the desired field first
-
-if (! is.na(opt$first_field)){
-  if (! opt$first_field %in% colnames(anno)){
-    die(paste(first_field, 'is not a valid field'))
-  }
-  anno <- anno[,c(opt$first_field, colnames(anno)[colnames(anno) != opt$first_field])]
-}
-
-# Version transcripts
-
-if ( opt$feature_type == 'transcript' && opt$version_transcripts && all(c('transcript_id', 'transcript_version') %in% colnames(anno) )){
-  has_transcript_version <- ! is.na(anno$transcript_version)
-  anno$transcript_id[has_transcript_version] <- paste(anno$transcript_id[has_transcript_version], anno$transcript_version[has_transcript_version], sep='.')
-}
-
-# If specified, filter down a provided cDNA FASTA file
-
-if (! is.null(opt$filter_cdnas)){
-  
-  print(paste("Filtering", opt$filter_cdnas, "to match the GTF"))
-  
-  suppressPackageStartupMessages(require(Biostrings))
-  
-  cdna <- readDNAStringSet(opt$filter_cdnas)
-  cdna_transcript_names <- unlist(lapply(names(cdna), function(x) unlist(strsplit(x, ' '))[1]  ))
-  
-  # Filter out cDNAs without matching transcript entries in the GTF
-  
-  if (! any(cdna_transcript_names %in% anno[[opt$filter_cdnas_field]])){
-    die(paste("ERROR: None of the input sequences have matching", opt$filter_cdnas_field, 'values in the GTF file'))
-  }
-  
-  cdna <- cdna[which(cdna_transcript_names %in% anno[[opt$filter_cdnas_field]])]
-  
-  print(paste('Storing filtered seqeunces to', opt$filter_cdnas_output))
-  writeXStringSet(x = cdna, filepath = opt$filter_cdnas_output, compress = 'gzip')
-}
-
-# If specified, subset to desired fields
-
-if (! is.null(opt$fields) && opt$fields != ''){
-  fields <- unlist(strsplit(opt$fields, ','))
-  if (any(! fields %in% colnames(anno))){
-    die(paste('ERROR:', fields, 'contains invalid field(s)'))
-  }
-  anno <- anno[,fields, drop = FALSE]
-  anno <- anno[apply(anno, 1, function(x) all(! is.na(x))), ]
-}
-
-print(paste('Storing output to', opt$output_file))
-write.table(anno, file = opt$output_file, sep = "\t", quote=FALSE, row.names = FALSE, col.names = opt$no_header)