Mercurial > repos > artbio > small_rna_maps
diff small_rna_maps.r @ 0:6d48150495e3 draft
planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/small_rna_maps commit d4d8106d66b65679a1a685ab94bfcf99cdb7b959
author | artbio |
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date | Mon, 24 Jul 2017 06:28:45 -0400 |
parents | |
children | 507383cce5a8 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/small_rna_maps.r Mon Jul 24 06:28:45 2017 -0400 @@ -0,0 +1,141 @@ +## Setup R error handling to go to stderr +options( show.error.messages=F, + error = function () { cat( geterrmessage(), file=stderr() ); q( "no", 1, F ) } ) +warnings() +library(RColorBrewer) +library(lattice) +library(latticeExtra) +library(grid) +library(gridExtra) +library(optparse) + +option_list <- list( + make_option(c("-r", "--output_tab"), type="character", help="path to tabular file"), + make_option(c("-s", "--sizes"), type="character", help="path to size dataframe"), + make_option("--output_pdf", type = "character", help="path to the pdf file with plot"), + make_option("--extra_plot", type = "character", help="what additional data should be plotted") + ) + +parser <- OptionParser(usage = "%prog [options] file", option_list = option_list) +args = parse_args(parser) +if (length(args$sizes) != 0) { args$extra_plot <- "SizeDistribution"} + +# dataset manipulation + +Table = read.delim(args$output_tab, header=T, row.names=NULL) +Table <- within(Table, Nbr_reads[Polarity=="R"] <- (Nbr_reads[Polarity=="R"]*-1)) +n_samples=length(unique(Table$Dataset)) +genes=unique(levels(Table$Chromosome)) +per_gene_readmap=lapply(genes, function(x) subset(Table, Chromosome==x)) +per_gene_limit=lapply(genes, function(x) c(1, unique(subset(Table, Chromosome==x)$Chrom_length)) ) +n_genes=length(per_gene_readmap) +if (args$extra_plot == "SizeDistribution") { + size=read.delim(args$sizes, header=T, row.names=NULL) + size <- within(size, Nbr_reads[Polarity=="R"] <- (Nbr_reads[Polarity=="R"]*-1)) + per_gene_size=lapply(genes, function(x) subset(size, Chromosome==x)) + } + +## end of data frames implementation + +## functions + +plot_readmap=function(df, ...) { + combineLimits(xyplot(Nbr_reads~Coordinate|factor(Dataset, levels=unique(Dataset))+factor(Chromosome, levels=unique(Chromosome)), + data=df, + type='h', + lwd=1.5, + scales= list(relation="free", x=list(rot=0, cex=0.7, axs="i", tck=0.5), y=list(tick.number=4, rot=90, cex=0.7)), + xlab=NULL, main=NULL, ylab=NULL, + as.table=T, + origin = 0, + horizontal=FALSE, + group=Polarity, + col=c("red","blue"), + par.strip.text = list(cex=0.7), + ...)) + } + + +plot_size=function(df, ...) { + #smR.prepanel=function(x,y,...) {; yscale=c(y*0, max(abs(y)));list(ylim=yscale);} + sizeplot = xyplot(eval(as.name(args$extra_plot))~Coordinate|factor(Dataset, levels=unique(Dataset))+factor(Chromosome, levels=unique(Chromosome)), + data=df, + type='p', + cex=0.35, + pch=19, + scales= list(relation="free", x=list(rot=0, cex=0, axs="i", tck=0.5), y=list(tick.number=4, rot=90, cex=0.7)), + xlab=NULL, main=NULL, ylab=NULL, + as.table=T, + origin = 0, + horizontal=FALSE, + group=Polarity, + col=c("darkred","darkblue"), + par.strip.text = list(cex=0.7), + ...) + combineLimits(sizeplot) + } + +plot_size_distribution= function(df, ...) { +# smR.prepanel=function(x,y,...){; yscale=c(-max(abs(y)), max(abs(y)));list(ylim=yscale);} + bc= barchart(Nbr_reads~as.factor(Size)|factor(Dataset, levels=unique(Dataset))+Chromosome, data = df, origin = 0, + horizontal=FALSE, +group=Polarity, +stack=TRUE, + col=c('red', 'blue'), + cex=0.75, + scales=list(y=list(tick.number=4, rot=90, relation="free", cex=0.7), x=list(cex=0.7) ), +# prepanel=smR.prepanel, + xlab = NULL, + ylab = NULL, + main = NULL, + as.table=TRUE, + newpage = T, + par.strip.text = list(cex=0.7), + ...) + combineLimits(bc) + } + + +## end of functions + +## function parameters +par.settings.readmap=list(layout.heights=list(top.padding=0, bottom.padding=0), strip.background = list(col=c("lightblue","lightgreen")) ) +par.settings.size=list(layout.heights=list(top.padding=0, bottom.padding=0)) +graph_title=list(Coverage="Read Maps and Coverages", Median="Read Maps and Median sizes", Mean="Read Maps and Mean sizes", SizeDistribution="Read Maps and Size Distributions") +graph_legend=list(Coverage="Read counts / Coverage", Median="Read counts / Median size", Mean="Read counts / Mean size", SizeDistribution="Read counts") +graph_bottom=list(Coverage="Nucleotide coordinates", Median="Nucleotide coordinates", Mean="Nucleotide coordinates", SizeDistribution="Read sizes / Nucleotide coordinates") +## end of function parameters' + +## GRAPHS + +if (n_genes > 5) {page_height_simple = 11.69; page_height_combi=11.69; rows_per_page=6} else { + rows_per_page= n_genes; page_height_simple = 2.5*n_genes; page_height_combi=page_height_simple*2 } +if (n_samples > 4) {page_width = 8.2677*n_samples/4} else {page_width = 8.2677*n_samples/2} # to test + + +pdf(file=args$output_pdf, paper="special", height=page_height_simple, width=page_width) +if (rows_per_page %% 2 != 0) { rows_per_page = rows_per_page + 1} +for (i in seq(1,n_genes,rows_per_page/2)) { + start=i + end=i+rows_per_page/2-1 + if (end>n_genes) {end=n_genes} + readmap_plot.list=lapply(per_gene_readmap[start:end], function(x) plot_readmap(x, strip=FALSE, par.settings=par.settings.readmap)) + if (args$extra_plot == "SizeDistribution") { + size_plot.list=lapply(per_gene_size[start:end], function(x) plot_size_distribution(x, par.settings=par.settings.size)) + } + else { + size_plot.list=lapply(per_gene_readmap[start:end], function(x) plot_size(x, par.settings=par.settings.size)) + } + + + plot.list=rbind(size_plot.list, readmap_plot.list) + args_list=c(plot.list, list(nrow=rows_per_page+1, ncol=1, + top=textGrob(graph_title[[args$extra_plot]], gp=gpar(cex=1), just="top"), + left=textGrob(graph_legend[[args$extra_plot]], gp=gpar(cex=1), vjust=1, rot=90), + sub=textGrob(graph_bottom[[args$extra_plot]], gp=gpar(cex=1), just="bottom") + ) + ) +do.call(grid.arrange, args_list) +} +devname=dev.off() +