diff goseq.r @ 0:a6427f7893b0 draft

planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/goseq_1_22_0 commit fdd0811efc61c31f88ff17096fbe8ee8cfacd766-dirty
author mvdbeek
date Fri, 26 Feb 2016 06:57:47 -0500
parents
children 81283f3d65c7
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/goseq.r	Fri Feb 26 06:57:47 2016 -0500
@@ -0,0 +1,85 @@
+sink(stdout(), type = "message")
+library(goseq)
+library(optparse)
+
+option_list <- list(
+    make_option(c("-d", "--dge_file"), type="character", help="Path to file with differential gene expression result"),
+    make_option(c("-w","--wallenius_tab"), type="character", help="Path to output file with P-values estimated using wallenius distribution."),
+    make_option(c("-s","--sampling_tab"), type="character", default=FALSE, help="Path to output file with P-values estimated using wallenius distribution."),
+    make_option(c("-n","--nobias_tab"), type="character", default=FALSE, help="Path to output file with P-values estimated using wallenius distribution and no correction for gene length bias."),
+    make_option(c("-l","--length_bias_plot"), type="character", default=FALSE, help="Path to length-bias plot."),
+    make_option(c("-sw","--sample_vs_wallenius_plot"), type="character", default=FALSE, help="Path to plot comparing sampling with wallenius p-values."),
+    make_option(c("-padj", "--p_adj_column"), type="integer",help="Column that contains p. adjust values"),
+    make_option(c("-c", "--cutoff"), type="double",dest="p_adj_cutoff",
+                help="Genes with p.adjust below cutoff are considered not differentially expressed and serve as control genes"),
+    make_option(c("-r", "--repcnt"), type="integer", default=100, help="Number of repeats for sampling"),
+    make_option(c("-lf", "--length_file"), default=FALSE, help = "Path to "),
+    make_option(c("-g", "--genome"), type="character", help = "Genome [used for looking up correct gene length]"),
+    make_option(c("-i", "--gene_id"), type="character", help="Gene ID of gene column in DGE file")
+  )
+parser <- OptionParser(usage = "%prog [options] file", option_list=option_list)
+args = parse_args(parser)
+
+# Vars:
+dge_file = args$dge_file
+p_adj_column = args$p_adj_colum
+p_adj_cutoff = args$p_adj_cutoff
+length_file = args$length_file
+genome = args$genome
+gene_id = args$gene_id
+wallenius_tab = args$wallenius_tab
+sampling_tab = args$sampling_tab
+nobias_tab = args$nobias_tab
+length_bias_plot = args$length_bias_plot
+sample_vs_wallenius_plot = args$sample_vs_wallenius_plot
+repcnt = args$repcnt
+
+
+# format DE genes into vector suitable for use with goseq
+dge_table = read.delim(dge_file, header = TRUE, sep="\t", check.names = FALSE)
+genes = as.integer(dge_table[,p_adj_column]<p_adj_cutoff)
+names(genes) = dge_table[,1] # Assuming first row contains gene names
+
+# Get gene lengths
+
+if (length_file) {
+  length_table = read.delim(length_file, header=TRUE, sep="\t", check.names=FALSE, row.names=TRUE)
+  gene_lengths = length_table[names(genes),]$length
+  } else {
+  gene_lengths = getlength(names(genes), genome, gene_id)
+  }
+
+# Estimate PWF
+
+pdf(length_bias_plot)
+pwf=nullp(genes, genome, gene_id, gene_lengths)
+dev.off()
+# wallenius approximation of p-values
+GO.wall=goseq(pwf, genome, gene_id)
+
+GO.nobias=goseq(pwf, genome, gene_id, method="Hypergeometric")
+
+# Sampling distribution
+if (repcnt > 0) {
+  GO.samp=goseq(pwf,genome, gene_id, method="Sampling", repcnt=repcnt)
+  # Compare sampling with wallenius
+  pdf(sample_vs_wallenius_plot)
+  plot(log10(GO.wall[,2]), log10(GO.samp[match(GO.samp[,1],GO.wall[,1]),2]),
+     xlab="log10(Wallenius p-values)",ylab="log10(Sampling p-values)",
+     xlim=c(-3,0))
+     abline(0,1,col=3,lty=2)
+  dev.off()
+  write.table(GO.samp, sampling_tab, sep="\t", row.names = FALSE, quote = FALSE)
+}
+
+
+write.table(GO.wall, wallenius_tab, sep="\t", row.names = FALSE, quote = FALSE)
+write.table(GO.nobias, nobias_tab, sep="\t", row.names = FALSE, quote = FALSE)
+
+sessionInfo()
+
+# Use the following to get a list of supported genomes / gene ids
+
+# write.table(supportedGenomes(), "available_genomes.tab", row.names = FALSE, quote=FALSE)
+# write.table(supportedGeneIDs(), "supported_gene_ids.tab", row.name = FALSE, quote = FALSE)
+# write.table(table.summary, "input_gene_count_matrix.tab", row.names = FALSE, quote = FALSE)