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author | proteore |
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date | Mon, 04 Dec 2017 09:39:21 -0500 |
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children | 829cbdb71efa |
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# enrichment_v3.R # Usage : Rscript --vanilla enrichment_v3.R --inputtype tabfile (or # copypaste) --input file.txt --ontology "BP/CC/MF" --option option (e.g # : classic/elim...) --threshold threshold --correction correction --textoutput # text --barplotoutput barplot # --dotplotoutput dotplot --column column --geneuniver human # e.g : Rscript --vanilla enrichment_v3.R --inputtype tabfile --input file.txt # --ontology BP --option classic --threshold 1e-15 --correction holm # --textoutput TRUE # --barplotoutput TRUE --dotplotoutput TRUE --column c1 --geneuniverse # org.Hs.eg.db # INPUT : # - type of input. Can be ids separated by a blank space (copypast), or a text # file (tabfile) # - file with at least one column of ensembl ids # - gene ontology category : Biological Process (BP), Cellular Component (CC), Molecular Function (MF) # - test option (relative to topGO algorithms) : elim, weight01, parentchild, or no option (classic) # - threshold for enriched GO term pvalues (e.g : 1e-15) # - correction for multiple testing (see p.adjust options : holm, hochberg, hommel, bonferroni, BH, BY,fdr,none # - outputs wanted in this order text, barplot, dotplot with boolean value (e.g # : TRUE TRUE TRUE ). # Declare the output not wanted as none # - column containing the ensembl ids if the input file is a tabfile # - gene universe reference for the user chosen specie # - header : if the input is a text file, does this text file have a header # (TRUE/FALSE) # # OUTPUT : # - outputs commanded by the user named respectively result.tsv for the text # results file, barplot.png for the barplot image file and dotplot.png for the # dotplot image file # loading topGO library library("topGO") '%!in%' <- function(x,y)!('%in%'(x,y)) # Parse command line arguments args = commandArgs(trailingOnly = TRUE) # create a list of the arguments from the command line, separated by a blank space hh <- paste(unlist(args),collapse=' ') # delete the first element of the list which is always a blank space listoptions <- unlist(strsplit(hh,'--'))[-1] # for each input, split the arguments with blank space as separator, unlist, # and delete the first element which is the input name (e.g --inputtype) options.args <- sapply(listoptions,function(x){ unlist(strsplit(x, ' '))[-1] }) # same as the step above, except that only the names are kept options.names <- sapply(listoptions,function(x){ option <- unlist(strsplit(x, ' '))[1] }) names(options.args) <- unlist(options.names) if (length(options.args) != 12) { stop("Not enough/Too many arguments", call. = FALSE) } typeinput = options.args[1] listfile = options.args[2] onto = as.character(options.args[3]) option = as.character(options.args[4]) correction = as.character(options.args[6]) threshold = as.numeric(options.args[5]) text = as.character(options.args[7]) barplot = as.character(options.args[8]) dotplot = as.character(options.args[9]) column = as.numeric(gsub("c","",options.args[10])) geneuniverse = as.character(options.args[11]) header = as.character(options.args[12]) if (typeinput=="copypaste"){ sample = as.data.frame(unlist(listfile)) sample = sample[,column] } if (typeinput=="tabfile"){ if (header=="TRUE"){ sample = read.table(listfile,header=TRUE,sep="\t",na.strings="NA",fill=TRUE) }else{ sample = read.table(listfile,header=FALSE,sep="\t",na.strings="NA",fill=TRUE) } sample = sample[,column] } # Launch enrichment analysis and return result data from the analysis or the null # object if the enrichment could not be done. goEnrichment = function(geneuniverse,sample,onto){ # get all the GO terms of the corresponding ontology (BP/CC/MF) and all their # associated ensembl ids according to the org package xx = annFUN.org(onto,mapping=geneuniverse,ID="ensembl") allGenes = unique(unlist(xx)) # check if the genes given by the user can be found in the org package (gene # universe), that is in # allGenes if (length(intersect(sample,allGenes))==0){ print("None of the input ids can be found in the org package data, enrichment analysis cannot be realized. \n The inputs ids probably have no associated GO terms.") return(c(NULL,NULL)) } geneList = factor(as.integer(allGenes %in% sample)) names(geneList) <- allGenes #topGO enrichment # Creation of a topGOdata object # It will contain : the list of genes of interest, the GO annotations and the GO hierarchy # Parameters : # ontology : character string specifying the ontology of interest (BP, CC, MF) # allGenes : named vector of type numeric or factor # annot : tells topGO how to map genes to GO annotations. # argument not used here : nodeSize : at which minimal number of GO annotations # do we consider a gene myGOdata = new("topGOdata", description="SEA with TopGO", ontology=onto, allGenes=geneList, annot = annFUN.org, mapping=geneuniverse,ID="ensembl") # Performing enrichment tests result <- runTest(myGOdata, algorithm=option, statistic="fisher") return(c(result,myGOdata)) } # Some libraries such as GOsummaries won't be able to treat the values such as # "< 1e-30" produced by topGO. As such it is important to delete the < char # with the deleteInfChar function. Nevertheless the user will have access to the original results in the text output. deleteInfChar = function(values){ lines = grep("<",values) if (length(lines)!=0){ for (line in lines){ values[line]=gsub("<","",values[line]) } } return(values) } corrMultipleTesting = function(result, myGOdata,correction,threshold){ # adjust for multiple testing if (correction!="none"){ # GenTable : transforms the result object into a list. Filters can be applied # (e.g : with the topNodes argument, to get for instance only the n first # GO terms with the lowest pvalues), but as we want to apply a correction we # take all the GO terms, no matter their pvalues allRes <- GenTable(myGOdata, test = result, orderBy = "result", ranksOf = "result",topNodes=length(attributes(result)$score)) # Some pvalues given by topGO are not numeric (e.g : "<1e-30). As such, these # values are converted to 1e-30 to be able to correct the pvalues pvaluestmp = deleteInfChar(allRes$test) # the correction is done from the modified pvalues allRes$qvalues = p.adjust(pvaluestmp, method = as.character(correction), n = length(pvaluestmp)) allRes = as.data.frame(allRes) # Rename the test column by pvalues, so that is more explicit nb = which(names(allRes) %in% c("test")) names(allRes)[nb] = "pvalues" allRes = allRes[which(as.numeric(allRes$pvalues) <= threshold),] if (length(allRes$pvalues)==0){ print("Threshold was too stringent, no GO term found with pvalue equal or lesser than the threshold value") return(NULL) } allRes = allRes[order(allRes$qvalues),] } if (correction=="none"){ # get all the go terms under user threshold mysummary <- summary(attributes(result)$score <= threshold) numsignif <- as.integer(mysummary[[3]]) # get all significant nodes allRes <- GenTable(myGOdata, test = result, orderBy = "result", ranksOf = "result",topNodes=numsignif) allRes = as.data.frame(allRes) # Rename the test column by pvalues, so that is more explicit nb = which(names(allRes) %in% c("test")) names(allRes)[nb] = "pvalues" if (numsignif==0){ print("Threshold was too stringent, no GO term found with pvalue equal or lesser than the threshold value") return(NULL) } allRes = allRes[order(allRes$pvalues),] } return(allRes) } # roundValues will simplify the results by rounding down the values. For instance 1.1e-17 becomes 1e-17 roundValues = function(values){ for (line in 1:length(values)){ values[line]=as.numeric(gsub(".*e","1e",as.character(values[line]))) } return(values) } createDotPlot = function(data, onto){ values = deleteInfChar(data$pvalues) values = roundValues(values) values = as.numeric(values) geneRatio = data$Significant/data$Annotated goTerms = data$Term count = data$Significant labely = paste("GO terms",onto,sep=" ") png(filename="dotplot.png",res=300, width = 3200, height = 3200, units = "px") sp1 = ggplot(data,aes(x=geneRatio,y=goTerms, color=values,size=count)) +geom_point() + scale_colour_gradientn(colours=c("red","violet","blue")) + xlab("Gene Ratio") + ylab(labely) + labs(color="p-values\n") plot(sp1) dev.off() } createBarPlot = function(data, onto){ values = deleteInfChar(data$pvalues) values = roundValues(values) values = as.numeric(values) goTerms = data$Term count = data$Significant png(filename="barplot.png",res=300, width = 3200, height = 3200, units = "px") labely = paste("GO terms",onto,sep=" ") p<-ggplot(data, aes(x=goTerms, y=count,fill=values)) + ylab("Gene count") + xlab(labely) +geom_bar(stat="identity") + scale_fill_gradientn(colours=c("red","violet","blue")) + coord_flip() + labs(fill="p-values\n") plot(p) dev.off() } # Produce the different outputs createOutputs = function(result, cut_result,text, barplot, dotplot, onto){ if (is.null(result)){ if (text=="TRUE"){ err_msg = "None of the input ids can be found in the org package data, enrichment analysis cannot be realized. \n The inputs ids probably either have no associated GO terms or are not ENSG identifiers (e.g : ENSG00000012048)." write.table(err_msg, file='result.csv', quote=FALSE, sep='\t', col.names = T, row.names = F) } if (barplot=="TRUE"){ png(filename="barplot.png") plot.new() #text(0,0,err_msg) dev.off() } if (dotplot=="TRUE"){ png(filename="dotplot.png") plot.new() #text(0,0,err_msg) dev.off() } return(TRUE) } if (is.null(cut_result)){ if (text=="TRUE"){ err_msg = "Threshold was too stringent, no GO term found with pvalue equal or lesser than the threshold value." write.table(err_msg, file='result.csv', quote=FALSE, sep='\t', col.names = T, row.names = F) } if (barplot=="TRUE"){ png(filename="barplot.png") plot.new() text(0,0,err_msg) dev.off() } if (dotplot=="TRUE"){ png(filename="dotplot.png") plot.new() text(0,0,err_msg) dev.off() } return(TRUE) } if (text=="TRUE"){ write.table(cut_result, file='result.csv', quote=FALSE, sep='\t', col.names = T, row.names = F) } if (barplot=="TRUE"){ createBarPlot(cut_result, onto) } if (dotplot=="TRUE"){ createDotPlot(cut_result, onto) } return(TRUE) } # Load R library ggplot2 to plot graphs library(ggplot2) # Launch enrichment analysis allresult = goEnrichment(geneuniverse,sample,onto) result = allresult[1][[1]] myGOdata = allresult[2][[1]] if (!is.null(result)){ # Adjust the result with a multiple testing correction or not and with the user # p-value cutoff cut_result = corrMultipleTesting(result,myGOdata, correction,threshold) }else{ cut_result=NULL } createOutputs(result, cut_result,text, barplot, dotplot, onto)