Mercurial > repos > bornea > apostl_static_bubblegraph_generator
changeset 14:8fe500f4e2cc draft
Deleted selected files
author | bornea |
---|---|
date | Wed, 11 May 2016 11:00:50 -0400 |
parents | 019ccec16de8 |
children | 651a602e0c7f |
files | bubbles_v9_NSAF_natural_log.R |
diffstat | 1 files changed, 0 insertions(+), 233 deletions(-) [+] |
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--- a/bubbles_v9_NSAF_natural_log.R Wed May 11 11:00:44 2016 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,233 +0,0 @@ -rm(list=ls()) -################################################################################################### -# R-code: Multi-bubble graph generation from SAINTexpress output -# Author: Brent Kuenzi -################################################################################################### -library(dplyr); library(tidyr); library(ggplot2) -################################################################################################### -### Run program ### - -## REQUIRED INPUT ## -# 1) listfile: SAINTexpress generated "list.txt" file -# 2) preyfile: SAINT pre-processing generated "prey.txt" file used to run SAINTexpress -## OPTIONAL INPUT ## -# 3) crapome: raw output from crapome Workflow 1 query (http://www.crapome.org) -# 4) color: bubble color (default = "red") -# - color= "crapome": color bubbles based on Crapome(%) -# - Also recognizes any color within R's built-in colors() vector -# 5) label: Adds gene name labels to bubbles within the "zoomed in" graphs (default = FALSE) -# 6) cutoff: Saintscore cutoff to be assigned for filtering the "zoomed in" graphs (default = 0.8) -################################################################################################### -main <- function(listfile, preyfile , crapome=FALSE, color="red", label=FALSE, cutoff=0.8, type="SC", inc_file = "None", exc_file = "None" ) { - cutoff_check(cutoff) - listfile <- list_type(listfile, inc_file, exc_file) - if(type == "SC") { - df <- merge_files_sc(listfile, preyfile, crapome) - } - if(type == "MQ") { - df <- merge_files_mq(listfile, preyfile, crapome) - } - bubble_NSAF(df,color) - bubble_SAINT(df,color) - bubble_zoom_SAINT(df, color, label, cutoff) - bubble_zoom_NSAF(df, color, label, cutoff) - write.table(df,"output.txt",sep="\t",quote=FALSE, row.names=FALSE) -} - -list_type <- function(df, inc_file, exc_file) { - Saint <- read.delim(df, stringsAsFactors=FALSE) - if (inc_file != "None") { - if (exc_file == "None"){ - inc_prots <- read.delim(inc_file, sep='\t', header=FALSE, stringsAsFactors=FALSE) - filtered_df = subset(Saint, Saint$Prey == inc_prots[,1]) - } - else { - inc_prots <- read.delim(inc_file, sep='\t', header=FALSE, stringsAsFactors=FALSE) - exc_prots <- read.delim(exc_file, sep='\t', header=FALSE, stringsAsFactors=FALSE) - filtered_df = subset(Saint, Saint$Prey == inc_prots[,1]) - filtered_df = subset(filtered_df, filtered_df$Prey != exc_prots[,1]) - } - } - else if (exc_file != "None") { - exc_prots <- read.delim(exc_file, sep='\t', header=FALSE, stringsAsFactors=FALSE) - filtered_df = subset(Saint, Saint$Prey != exc_prots[,1]) - } - else { - filtered_df = Saint - } - return(filtered_df) - -} -################################################################################################### -# Merge input files and caculate Crapome(%) and NSAF for each protein for each bait -################################################################################################### -merge_files_mq <- function(SAINT, prey_DF, crapome=FALSE) { - #SAINT <- read.table(SAINT_DF, sep='\t', header=TRUE) - prey <- read.table(prey_DF, sep='\t', header=FALSE); colnames(prey) <- c("Prey", "Length", "PreyGene") - DF <- merge(SAINT,prey) - DF$SpecSum <- log2(DF$SpecSum) - - if(crapome!=FALSE) { - crapome <- read.table(crapome, sep='\t', header=TRUE) - colnames(crapome) <- c("Prey", "Symbol", "Num.of.Exp", "Ave.SC", "Max.SC") - DF1 <- merge(DF, crapome); as.character(DF1$Num.of.Exp); DF1$Symbol <- NULL; - DF1$Ave.SC <- NULL; DF1$Max.SC <- NULL #remove unnecessary columns - DF1$Num.of.Exp <- sub("^$", "0 / 1", DF1$Num.of.Exp ) #replace blank values with 0 / 1 - DF <- DF1 %>% separate(Num.of.Exp, c("NumExp", "TotalExp"), " / ") #split into 2 columns - DF$CrapomePCT <- 100 - (as.integer(DF$NumExp) / as.integer(DF$TotalExp) * 100) #calculate crapome % - } - DF$SAF <- DF$AvgSpec / DF$Length - DF2 = DF %>% group_by(Bait) %>% mutate(NSAF = SAF/sum(SAF)) - DF$NSAF = DF2$NSAF - return(DF) -} - -merge_files_sc <- function(SAINT, prey_DF, crapome=FALSE) { - #SAINT <- read.table(SAINT_DF, sep='\t', header=TRUE) - prey <- read.table(prey_DF, sep='\t', header=FALSE); colnames(prey) <- c("Prey", "Length", "PreyGene") - DF <- merge(SAINT,prey) - - if(crapome!=FALSE) { - crapome <- read.table(crapome, sep='\t', header=TRUE) - colnames(crapome) <- c("Prey", "Symbol", "Num.of.Exp", "Ave.SC", "Max.SC") - DF1 <- merge(DF, crapome); as.character(DF1$Num.of.Exp); DF1$Symbol <- NULL; - DF1$Ave.SC <- NULL; DF1$Max.SC <- NULL #remove unnecessary columns - DF1$Num.of.Exp <- sub("^$", "0 / 1", DF1$Num.of.Exp ) #replace blank values with 0 / 1 - DF <- DF1 %>% separate(Num.of.Exp, c("NumExp", "TotalExp"), " / ") #split into 2 columns - DF$CrapomePCT <- 100 - (as.integer(DF$NumExp) / as.integer(DF$TotalExp) * 100) #calculate crapome % - } - DF$SAF <- DF$AvgSpec / DF$Length - DF2 = DF %>% group_by(Bait) %>% mutate(NSAF = SAF/sum(SAF)) - DF$NSAF = DF2$NSAF - return(DF) -} -################################################################################################### -# Plot all proteins for each bait by x=ln(NSAF), y=Log2(FoldChange) -################################################################################################### -bubble_NSAF <- function(data, color) { - if(color=="crapome") { - a <- subset(data, CrapomePCT <80, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait)) - b <- subset(data, CrapomePCT>=80, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait)) - p <- qplot(x=log(NSAF), y=log2(FoldChange), data=a, colour=I("tan"),size=SpecSum) + scale_size(range=c(1,10)) + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) - if(length(levels(a$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} # multiple graphs if multiple baits - p <- p + geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum, color=CrapomePCT), data=b) + - scale_colour_gradient(limits=c(80, 100), low="tan", high="red") + - labs(colour="CRAPome Probability \nof Specific Interaction (%)", x="ln(NSAF)") + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=b) - return(ggsave(p, width=8,height=4,filename = "bubble_NSAF.png")) - } - if(color != "crapome") { - p <- qplot(x=log(NSAF), y=log2(FoldChange), data=data, colour=I(color),size=SpecSum) + scale_size(range=c(1,10)) + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=data) + # add bubble outlines - labs(x="ln(NSAF)") - if(length(levels(data$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - return(ggsave(p, width=8,height=4,filename = "bubble_NSAF.png")) - } - } -################################################################################################### -# Plot all proteins for each bait by x=Saintscore, y=Log2(FoldChange) -################################################################################################### -bubble_SAINT <- function(data, color) { - if(color=="crapome") { - a <- subset(data, CrapomePCT <80, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait)) #filter on CRAPome - b <- subset(data, CrapomePCT >=80, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait)) - p <- qplot(x=SaintScore, y=log2(FoldChange), data=a, colour=I("tan"),size=SpecSum) + - scale_size(range=c(1,10)) + geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) - if(length(levels(a$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - p <- p + geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum, color=CrapomePCT), data=b) + - scale_colour_gradient(limits=c(80, 100), low="tan", high="red") + - labs(colour="CRAPome Probability \nof Specific Interaction (%)") + - geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=b) - return(ggsave(p, width=8,height=4,filename = "bubble_SAINT.png")) - } - if(color != "crapome") { - p <- qplot(x=SaintScore, y=log2(FoldChange), data=data, colour=I(color),size=SpecSum) + - scale_size(range=c(1,10)) + geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=data) - if(length(levels(data$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - return(ggsave(p, width=8,height=4,filename = "bubble_SAINT.png")) - } - } -################################################################################################### -# Filter proteins on Saintscore cutoff and plot for each bait x=Saintscore, y=Log2(FoldChange) -################################################################################################### -bubble_zoom_SAINT <- function(data, color, label=FALSE, cutoff=0.8) { - if(color=="crapome") { - a <- subset(data, CrapomePCT <80 & SaintScore>=cutoff, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait, PreyGene)) - b <- subset(data, CrapomePCT >=80 & SaintScore >=cutoff, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait, PreyGene)) - p <- qplot(x=SaintScore, y=log2(FoldChange), data=a, colour=I("tan"),size=SpecSum) + - scale_size(range=c(1,10)) + ggtitle("Filtered on SAINT score")+geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) - if(label==TRUE & length(a$NSAF!=0)) { - p <- p + geom_text(data=a, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black") - } - if(length(levels(a$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - p <- p + geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum, color=CrapomePCT), data=b) + - scale_colour_gradient(limits=c(80, 100), low="tan", high="red") + - labs(colour="CRAPome Probability \nof Specific Interaction (%)") + - geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=b) - if(label==TRUE & length(b$NSAF!=0)) { - p <- p + geom_text(data=b, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black", show_guide=FALSE) - } - return(ggsave(p, width=8,height=4,filename = "bubble_zoom_SAINT.png")) - } - if(color != "crapome") { - a <- subset(data, SaintScore>=cutoff, select = c(NSAF,SpecSum, FoldChange, SaintScore, Bait, PreyGene)) - p <- qplot(x=SaintScore, y=log2(FoldChange), data=a, colour=I(color),size=SpecSum) + - scale_size(range=c(1,10)) + ggtitle("Filtered on SAINT score") + - geom_point(aes(x=SaintScore,y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) - if(label==TRUE & length(a$NSAF!=0)) { - p <- p + geom_text(data=a, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black", show_guide=FALSE) - } - if(length(levels(data$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - return(ggsave(p, width=8,height=4,filename = "bubble_zoom_SAINT.png")) - } -} -################################################################################################### -# Filter proteins on Saintscore cutoff and plot for each bait x=log(NSAF), y=Log2(FoldChange) -################################################################################################### -bubble_zoom_NSAF <- function(data, color, label=FALSE, cutoff=0.8) { - if(color=="crapome") { - a <- subset(data, CrapomePCT <80 & SaintScore>=cutoff, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait, PreyGene)) - b <- subset(data, CrapomePCT >=80 & SaintScore >=cutoff, select = c(NSAF,SpecSum, CrapomePCT, FoldChange, SaintScore, Bait, PreyGene)) - p <- qplot(x=log(NSAF), y=log2(FoldChange), data=a, colour=I("tan"),size=SpecSum) + - scale_size(range=c(1,10)) + ggtitle("Filtered on SAINT score") + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) - if(label==TRUE & length(a$NSAF!=0)) { - p <- p + geom_text(data=a, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black") - } - if(length(levels(a$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - p <- p + geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum, color=CrapomePCT), data=b) + - scale_colour_gradient(limits=c(80, 100), low="tan", high="red") + - labs(colour="CRAPome Probability \nof Specific Interaction (%)", x="ln(NSAF)") + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=b) - if(label==TRUE & length(b$NSAF!=0)) { - p <- p + geom_text(data=b, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black", show_guide=FALSE) - } - return(ggsave(p, width=8,height=4,filename = "bubble_zoom_NSAF.png")) - } - if(color != "crapome") { - a <- subset(data, SaintScore>=cutoff, select = c(NSAF,SpecSum, FoldChange, SaintScore, Bait, PreyGene)) - p <- qplot(x=log(NSAF), y=log2(FoldChange), data=a, colour=I(color), size=SpecSum) + - scale_size(range=c(1,10)) + ggtitle("Filtered on SAINT score") + - geom_point(aes(x=log(NSAF),y=log2(FoldChange), size=SpecSum), colour="black", shape=21, data=a) + - labs(x="ln(NSAF)") - if(label==TRUE & length(a$NSAF!=0)) { - p <- p + geom_text(data=a, aes(label=PreyGene, size=10, vjust=0, hjust=0),colour="black", show_guide=FALSE) - } - if(length(levels(data$Bait) > 1)) {p <- p + facet_wrap(~Bait, scales="free_y")} - return(ggsave(p, width=8,height=4,filename = "bubble_zoom_NSAF.png")) - } -} -################################################################################################### -# Check Saintscore cutoff and stop program if not between 0 and 1 -################################################################################################### -cutoff_check <- function(cutoff){ - if( any(cutoff < 0 | cutoff > 1) ) stop('SAINT score cutoff not between 0 and 1. Please correct and try again') -} - -args <- commandArgs(trailingOnly = TRUE) -main(args[1],args[2],args[3],args[4],args[5],args[6],args[7],args[8],args[9]) - -#main("test_list.txt", "preytest.txt", crapome="craptest.txt", color="crapome", label=TRUE) -#main("Crizo_list.txt", "prey_cr.txt", crapome = "crizo_crap.txt", color="crapome", label=TRUE, cutoff=0.7) -#main("test_list.txt", "preytest.txt", crapome=FALSE, color="magenta", label=FALSE, cutoff=1.1) \ No newline at end of file