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Lint R scripts

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This commit is contained in:
Bryan Roessler
2024-08-13 15:59:18 -04:00
parent f190967383
commit 79862ddab4
4 changed files with 185 additions and 170 deletions
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8
workflow/apps/r/addShiftVals.R
View File

@@ -10,25 +10,25 @@ library(sos)
args <- commandArgs(TRUE)
if (length(args) >= 1) {
finalTable <- args[1]
finalTable <- file.path(args[1])
} else {
finalTable <- "REMcRdy_lm_only.csv-finalTable.csv" # for legacy workflow
}
if (length(args) >= 2) {
shiftFile <- args[2]
shiftFile <- file.path(args[2])
} else {
shiftFile <- "Shift_only.csv" # for legacy workflow
}
if (length(args) >= 3) {
studyInfo <- args[3]
studyInfo <- file.path(args[3])
} else {
studyInfo <- "../Code/StudyInfo.csv" # for legacy workflow
}
if (length(args) >= 4) {
output <- args[4]
output <- file.path(args[4])
} else {
output <- "REMcHeatmaps/REMcWithShift.csv" # for legacy workflow
}

14
workflow/apps/r/createHeatMaps.R
View File

@@ -171,7 +171,7 @@ for (i in 1:num_unique_clusts) {
if (cluster_length != 1) {
X0 <- as.matrix(cluster_data[, 4:(length(hmapfile[1, ]) - 2)])
if (cluster_length >= 2001) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 20, width = 15)
heatmap.2(
x = X0,
@@ -191,7 +191,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length >= 201 && cluster_length <= 2000) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 15, width = 12)
heatmap.2(
x = X0,
@@ -210,7 +210,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length >= 150 && cluster_length <= 200) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 12, width = 12)
heatmap.2(
x = X0,
@@ -228,7 +228,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length >= 101 && cluster_length <= 149) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, mypath, height = 12, width = 12)
heatmap.2(
x = X0,
@@ -246,7 +246,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length >= 60 && cluster_length <= 100) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 12, width = 12)
heatmap.2(
x = X0,
@@ -264,7 +264,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length <= 59 && cluster_length >= 30) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 9, width = 12)
heatmap.2(
x = X0,
@@ -282,7 +282,7 @@ for (i in 1:num_unique_clusts) {
dev.off()
}
if (cluster_length <= 29) {
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), sep = ""), ".pdf")
mypath <- file.path(outDir, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 7, width = 12)
heatmap.2(
x = X0,

332
workflow/apps/r/createHeatMapsHomology.R
View File

@@ -8,57 +8,58 @@ library(tidyverse)
args <- commandArgs(TRUE)
# Need to give the input "finalTable.csv" file after running REMc generated by eclipse
inputFinalTable <- args[1]
inputFinalTable <- file.path(args[1])
# Give the DAmP_list.txt as the third argument - will color the gene names differently
DAmPs <- Args[2]
DAmP_list <- read.delim(file=DAmPs,header=F,stringsAsFactors = F)
DAmPs <- file.path(Args[2])
DAmP_list <- read.delim(file = DAmPs, header = FALSE, stringsAsFactors = FALSE)
# Give the yeast human homology mapping as the fourth argument - will add the genes to the finalTable and use info for heatmaps
mapFile <- Args[3]
mapping <- read.csv(file=mapFile,stringsAsFactors = F)
mapFile <- file.path(Args[3])
mapping <- read.csv(file = mapFile, stringsAsFactors = FALSE)
# Define the output path for the heatmaps - create this folder first - in linux terminal in the working folder use > mkdir filename_heatmaps
outputPath <- Args[4]
outputPath <- file.path(Args[4])
# Read in finalTablewithShift
hmapfile <- data.frame(read.csv(file=inputFinalTable,header=TRUE,sep=",",stringsAsFactors = FALSE))
hmapfile <- data.frame(read.csv(file = inputFinalTable, header = TRUE, sep = ",", stringsAsFactors = FALSE))
# Map the finalTable to the human homolog file
hmapfile_map <- hmapfile
# Match using OrfRep after dropping the _1 _2 _3 _4
# Match using OrfRep after dropping the _1 _2 _3 _4
# But need to also account for some older files have ORF as column name rather than OrfRep in finalTable file
if(colnames(hmapfile_map)[2] == "OrfRep"){
if (colnames(hmapfile_map)[2] == "OrfRep") {
try(hmapfile_map$ORFMatch <- hmapfile_map$OrfRep)
}
if(colnames(hmapfile_map)[2] == "ORF"){
if (colnames(hmapfile_map)[2] == "ORF") {
try(hmapfile_map$ORFMatch <- hmapfile_map$ORF)
}
hmapfile_map$ORFMatch <- gsub("_1","",x=hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_2","",x=hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_3","",x=hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_4","",x=hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_1", "", x = hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_2", "", x = hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_3", "", x = hmapfile_map$ORFMatch)
hmapfile_map$ORFMatch <- gsub("_4", "", x = hmapfile_map$ORFMatch)
# Join the hmapfile using
hmapfile_w_homolog <- full_join(hmapfile_map,mapping,by=c("ORFMatch"="ensembl_gene_id"))
# Join the hmapfile using
hmapfile_w_homolog <- full_join(hmapfile_map, mapping, by = c("ORFMatch" = "ensembl_gene_id"))
# Remove matches that are not from the finalTable
hmapfile_w_homolog <- hmapfile_w_homolog[is.na(hmapfile_w_homolog$likelihood) == F,]
hmapfile_w_homolog <- hmapfile_w_homolog[is.na(hmapfile_w_homolog$likelihood) == FASLE, ]
# Write csv with all info from mapping file
write.csv(hmapfile_w_homolog,file=paste(outputPath,"/",inputFinalTable,"_WithHomologAll.csv",sep=""),row.names = F)
write.csv(hmapfile_w_homolog, file.path(outputPath, paste(inputFinalTable, "_WithHomologAll.csv", sep = "")), row.names = FALSE)
# Remove the non matches and output another mapping file - this is also one used to make heatmaps
hmapfile_w_homolog <- hmapfile_w_homolog[is.na(hmapfile_w_homolog$external_gene_name_Human) == F,]
write.csv(hmapfile_w_homolog,file=paste(outputPath,"/",inputFinalTable,"_WithHomologMatchesOnly.csv",sep=""),row.names = F)
hmapfile_w_homolog <- hmapfile_w_homolog[is.na(hmapfile_w_homolog$external_gene_name_Human) == FALSE, ]
write.csv(hmapfile_w_homolog, file.path(outputPath, paste(inputFinalTable, "_WithHomologMatchesOnly.csv", sep = ""), row.names = FALSE))
# Add human gene name to the Gene column
hmapfile_w_homolog$Gene <- paste(hmapfile_w_homolog$Gene,hmapfile_w_homolog$external_gene_name_Human,sep="/")
hmapfile_w_homolog$Gene <- paste(hmapfile_w_homolog$Gene, hmapfile_w_homolog$external_gene_name_Human, sep = "/")
# Only keep the finalTable file columns and the homology info
hmap_len <- dim(hmapfile)[2]
hmapfile_w_homolog_remake <- cbind(hmapfile_w_homolog[,1:hmap_len], hsapiens_homolog_orthology_type=hmapfile_w_homolog$hsapiens_homolog_orthology_type)
hmapfile_w_homolog_remake <-
cbind(hmapfile_w_homolog[, 1:hmap_len], hsapiens_homolog_orthology_type = hmapfile_w_homolog$hsapiens_homolog_orthology_type)
hmapfile <- hmapfile_w_homolog_remake
# Set NAs to NA
@@ -68,19 +69,20 @@ hmapfile[hmapfile == 0.001] <- NA
hmapfile[hmapfile == -0.001] <- NA
# Select the number of rows based on the number of genes
num_total_genes <- length(hmapfile[,1])
num_total_genes <- length(hmapfile[, 1])
# break out the cluster names so each part of the cluster origin can be accessed
# line below removed because it adds to many genes to clusters when going past 1-0-10 since it cannot differentiate between 1-0-1 and 1-0-10 when using grepl.
# hmapfile$cluster.origin = gsub(" ","",x=hmapfile$cluster.origin)
# Break out the cluster names so each part of the cluster origin can be accessed
# Line below removed because it adds to many genes to clusters when going past 1-0-10
# since it cannot differentiate between 1-0-1 and 1-0-10 when using grepl.
# hmapfile$cluster.origin = gsub(" ","",x = hmapfile$cluster.origin)
hmapfile$cluster.origin = gsub(";"," ;",x=hmapfile$cluster.origin)
hmapfile$cluster.origin = strsplit(hmapfile$cluster.origin,';')
hmapfile$cluster.origin <- gsub(";", " ;", x = hmapfile$cluster.origin)
hmapfile$cluster.origin <- strsplit(hmapfile$cluster.origin, ";")
# use tail(x,n) for accessing the outward most cluster
clust_rounds <- 0
for(i in 1:num_total_genes){
if(length(hmapfile$cluster.origin[[i]]) > clust_rounds){
for (i in 1:num_total_genes) {
if (length(hmapfile$cluster.origin[[i]]) > clust_rounds) {
clust_rounds <- length(hmapfile$cluster.origin[[i]])
}
}
@@ -89,12 +91,13 @@ unique_clusts <- unique(hmapfile$cluster.origin[1:num_total_genes])
unique_clusts <- unique_clusts[unique_clusts != " "]
#select only the unique cluster names
unique_clusts <- sort(unique(unlist(unique_clusts,use.names= FALSE)),decreasing=FALSE)
unique_clusts <- sort(unique(unlist(unique_clusts, use.names = FALSE)), decreasing = FALSE)
num_unique_clusts <- length(unique_clusts)
# Base the color key on a statistical analysis of the L and K data
# need to create "breaks" to set the color key, need to have 12 different breaks (for 11 colors)
# scale() will calculate the mean and standard deviation of the entire vector, then "scale" each element by those values by subtracting the mean and dividing by the sd.
# scale() will calculate the mean and standard deviation of the entire vector
# then "scale" each element by those values by subtracting the mean and dividing by the sd
# hmapfile[,4:(length(hmapfile[1,]) - 2)] <- scale(hmapfile[,4:(length(hmapfile[1,]) - 2)])
@@ -107,19 +110,19 @@ L_MAX <- 0
KcolumnValues <- vector()
LcolumnValues <- vector()
for(i in 4:(length(hmapfile[1,]) - 3)){
if(grepl("_Z_lm_K",colnames(hmapfile)[i],fixed=TRUE) == TRUE){
KcolumnValues <- append(KcolumnValues,i)
for (i in 4:(length(hmapfile[1, ]) - 3)){
if (grepl("_Z_lm_K", colnames(hmapfile)[i], fixed = TRUE) == TRUE) {
KcolumnValues <- append(KcolumnValues, i)
}
if(grepl("_Z_lm_L",colnames(hmapfile)[i],fixed=TRUE) == TRUE){
LcolumnValues <- append(LcolumnValues,i)
if (grepl("_Z_lm_L", colnames(hmapfile)[i], fixed = TRUE) == TRUE) {
LcolumnValues <- append(LcolumnValues, i)
}
}
# L_MAX <- quantile(hmapfile[,LcolumnValues],c(0,.01,.5,.99,1),na.rm=TRUE)[4]
# K_MIN <- quantile(hmapfile[,KcolumnValues],c(0,.01,.5,.99,1),na.rm=TRUE)[2]
# L_MAX <- quantile(hmapfile[,LcolumnValues],c(0,.01,.5,.975,1),na.rm=TRUE)[4]
# K_MIN <- quantile(hmapfile[,KcolumnValues],c(0,.025,.5,.99,1),na.rm=TRUE)[2]
# L_MAX <- quantile(hmapfile[,LcolumnValues],c(0,.01,.5,.99,1),na.rm = TRUE)[4]
# K_MIN <- quantile(hmapfile[,KcolumnValues],c(0,.01,.5,.99,1),na.rm = TRUE)[2]
# L_MAX <- quantile(hmapfile[,LcolumnValues],c(0,.01,.5,.975,1),na.rm = TRUE)[4]
# K_MIN <- quantile(hmapfile[,KcolumnValues],c(0,.025,.5,.99,1),na.rm = TRUE)[2]
# Z scores are
L_MAX <- 12
@@ -128,7 +131,7 @@ K_MIN <- -12
# L_Multiplier <- as.numeric(abs(K_MIN/L_MAX))
# hmapfile[,LcolumnValues] <- hmapfile[,LcolumnValues] * L_Multiplier
# if(grepl("SHIFT",colnames(hmapfile)[4],fixed=TRUE) == TRUE){
# if(grepl("SHIFT",colnames(hmapfile)[4],fixed = TRUE) == TRUE){
# print("FOUND SHIFT VALUES")
# hmapfile[,(LcolumnValues - 1)] <- hmapfile[,(LcolumnValues-1)] * L_Multiplier
# }
@@ -142,15 +145,19 @@ print(KEY_MIN)
print(L_MAX)
#print(L_Multiplier)
colormapbreaks <- c(KEY_MIN,KEY_MIN*(5/6),KEY_MIN*(4/6),KEY_MIN*(3/6),KEY_MIN*(2/6),KEY_MIN*(1/6),KEY_MAX*(1/6),KEY_MAX*(2/6),KEY_MAX*(3/6),KEY_MAX*(4/6),KEY_MAX*(5/6),KEY_MAX)
#print(colormapbreaks)
colormapbreaks <- c(KEY_MIN, KEY_MIN * (5 / 6), KEY_MIN * (4 / 6), KEY_MIN * (3 / 6),
KEY_MIN * (2 / 6), KEY_MIN * (1 / 6), KEY_MAX * (1 / 6), KEY_MAX * (2 / 6),
KEY_MAX * (3 / 6), KEY_MAX * (4 / 6), KEY_MAX * (5 / 6), KEY_MAX)
# print(colormapbreaks)
# Probably should give a way to detect shift in case that is is not in the first row... (maybe just grepl for the whole column name?)
# However since also using this to amend the first part. Could possibly identify all the ones that contain the word shift and then create an object containing just those numbers
# then could just use these values and create spaces only between interaction values - possibly could get rid of redundant shift values if we don't want to view these
# However since also using this to amend the first part.
# Could possibly identify all the ones that contain the word shift and then create an object containing just those numbers
# then could just use these values and create spaces only between interaction values
# possibly could get rid of redundant shift values if we don't want to view these
# could we pool all the shift data/average it?
if(grepl("Shift",colnames(hmapfile)[4],fixed=TRUE) == TRUE){
even_columns <- seq(from= 2, to= (length(hmapfile[1,]) - 7),by=2)
if (grepl("Shift", colnames(hmapfile)[4], fixed = TRUE) == TRUE) {
even_columns <- seq(from = 2, to = (length(hmapfile[1, ]) - 7), by = 2)
# ev_repeat = rep("white",length(even_columns))
# ev_repeat = rep("red",(length(hmapfile[1,]) - 5))
# middle_col <- (length(hmapfile[1,]) - 5)/2
@@ -158,8 +165,8 @@ if(grepl("Shift",colnames(hmapfile)[4],fixed=TRUE) == TRUE){
# print(ev_repeat)
}
if(grepl("Shift",colnames(hmapfile)[4],fixed=TRUE) == FALSE){
even_columns <- seq(from= 2, to= (length(hmapfile[1,]) - 7),by=1)
if (grepl("Shift", colnames(hmapfile)[4], fixed = TRUE) == FALSE) {
even_columns <- seq(from = 2, to = (length(hmapfile[1, ]) - 7), by = 1)
print("NO SHIFT VALS FOUND")
}
@@ -167,43 +174,43 @@ if(grepl("Shift",colnames(hmapfile)[4],fixed=TRUE) == FALSE){
# even_columns <- c(2,5,7,10,12,15,17)
# m <- 0
colnames_edit <- as.character(colnames(hmapfile)[4:(length(hmapfile[1,]) - 3)])
colnames_edit <- as.character(colnames(hmapfile)[4:(length(hmapfile[1, ]) - 3)])
colnames(DAmP_list)[1] <- "ORF"
hmapfile$DAmPs <- "YKO"
colnames(hmapfile)[2] <- "ORF"
try(hmapfile[hmapfile$ORF %in% DAmP_list$ORF,]$DAmPs <- "YKD")
try(hmapfile[hmapfile$ORF %in% DAmP_list$ORF, ]$DAmPs <- "YKD")
# X <- X[order(X$DAmPs,decreasing = TRUE),]
hmapfile$color2 <- NA
try(hmapfile[hmapfile$DAmPs == "YKO",]$color2 <- "black")
try(hmapfile[hmapfile$DAmPs == "YKD",]$color2 <- "red")
try(hmapfile[hmapfile$DAmPs == "YKO", ]$color2 <- "black")
try(hmapfile[hmapfile$DAmPs == "YKD", ]$color2 <- "red")
hmapfile$color <- NA
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_many2many",]$color <- "#F8766D")
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_one2many",]$color <- "#00BA38")
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_one2one",]$color <- "#619CFF")
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_many2many", ]$color <- "#F8766D")
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_one2many", ]$color <- "#00BA38")
try(hmapfile[hmapfile$hsapiens_homolog_orthology_type == "ortholog_one2one", ]$color <- "#619CFF")
# print(colnames_edit)
for(i in 1:length(colnames_edit)){
if(grepl("Shift",colnames_edit[i],fixed=TRUE) == TRUE){
for (i in 1:length(colnames_edit)) {
if (grepl("Shift", colnames_edit[i], fixed = TRUE) == TRUE) {
colnames_edit[i] <- ""
colnames_edit[i+1] <- gsub(pattern = "_Z_lm_",replacement = " ",x = colnames_edit[i+1])
try(colnames_edit[i+1] <- gsub(pattern = "_",replacement = " ",x = colnames_edit[i+1]))
colnames_edit[i + 1] <- gsub(pattern = "_Z_lm_", replacement = " ", x = colnames_edit[i + 1])
try(colnames_edit[i + 1] <- gsub(pattern = "_", replacement = " ", x = colnames_edit[i + 1]))
# INT_store <- strsplit(colnames_edit[i+1], "Z_lm")
# print(length(unlist(INT_store)))
# if(length(unlist(INT_store)) == 4){
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[3],sep=" ")
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[3],sep = " ")
# }
# if(length(unlist(INT_store)) == 3){
#
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],sep=" ")
#
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],sep = " ")
# }
# if(length(unlist(INT_store)) == 5){
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[3],unlist(INT_store)[4],sep=" ")
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[3],unlist(INT_store)[4],sep = " ")
# }
# if(length(unlist(INT_store)) == 6){
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[6],sep=" ")
# colnames_edit[i+1] <- paste(unlist(INT_store)[1],unlist(INT_store)[2],unlist(INT_store)[6],sep = " ")
# }
}
@@ -217,135 +224,142 @@ print(colnames_edit)
# colnames_edit[20] <- "TEM HL L"
# Create the heatmaps
for(i in 1:num_unique_clusts){
for (i in 1:num_unique_clusts) {
cluster <- unique_clusts[i]
cluster_data <- subset(hmapfile,grepl(cluster,cluster.origin))
cluster_length <- length(cluster_data[,1])
if(cluster_length != 1){
X0 <- as.matrix(cluster_data[,4:(length(hmapfile[1,]) - 6)])
if(cluster_length >= 2001){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=20,width=15)
cluster_data <- subset(hmapfile, grepl(cluster, cluster.origin))
cluster_length <- length(cluster_data[, 1])
if (cluster_length != 1) {
X0 <- as.matrix(cluster_data[, 4:(length(hmapfile[1, ]) - 6)])
if (cluster_length >= 2001) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 20, width = 15)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.1, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor= "white", offsetCol = 0.1,
# zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
# cellnote = round(X0,digits=0), notecex = 0.1, key=TRUE,
keysize=0.7, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
# ColSideColors=ev_repeat,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
# abline(v=0.5467,col="black")
# cellnote = round(X0,digits = 0), notecex = 0.1, key = TRUE,
keysize = 0.7, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
# ColSideColors = ev_repeat,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
# abline(v = 0.5467,col = "black")
dev.off()
}
if(cluster_length >= 201 && cluster_length <= 2000){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=15,width=12)
if (cluster_length >= 201 && cluster_length <= 2000) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 15, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.1, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
# zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.1, key=TRUE,
keysize=0.7, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
# abline(v=0.5316,col="black")
cellnote = round(X0, digits = 0), notecex = 0.1, key = TRUE,
keysize = 0.7, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
# abline(v = 0.5316,col = "black")
dev.off()
}
if(cluster_length >= 150 && cluster_length <= 200){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=12,width=12)
if (cluster_length >= 150 && cluster_length <= 200) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 12, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.1, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
# zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.2, key=TRUE,
keysize=1, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
cellnote = round(X0, digits = 0), notecex = 0.2, key = TRUE,
keysize = 1, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
dev.off()
}
if(cluster_length >= 101 && cluster_length <= 149){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,mypath,height=12,width=12)
if (cluster_length >= 101 && cluster_length <= 149) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 12, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.2, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
# zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.3, key=TRUE,
keysize=1, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
cellnote = round(X0, digits = 0), notecex = 0.3, key = TRUE,
keysize = 1, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
dev.off()
}
if(cluster_length >= 60 && cluster_length <= 100){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=12,width=12)
if (cluster_length >= 60 && cluster_length <= 100) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 12, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.4, scale = "none",
breaks=colormapbreaks,symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
#zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.3, key=TRUE,
keysize=1, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
cellnote = round(X0, digits = 0), notecex = 0.3, key = TRUE,
keysize = 1, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
dev.off()
}
if(cluster_length <= 59 && cluster_length >= 30){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=9,width=12)
if (cluster_length <= 59 && cluster_length >= 30) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 9, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA, distfun = dist, hclustfun = hclust,
x = X0,
Rowv = TRUE, Colv = NA, distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.6, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
#zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.4, key=TRUE,
keysize=1, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
cellnote = round(X0, digits = 0), notecex = 0.4, key = TRUE,
keysize = 1, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
dev.off()
}
if(cluster_length <= 29){
mypath = file.path(outputPath,paste("cluster_",gsub(" ","",cluster), ".pdf",sep=""))
pdf(file=mypath,height=7,width=12)
if (cluster_length <= 29) {
mypath <- file.path(outputPath, paste("cluster_", gsub(" ", "", cluster), ".pdf", sep = ""))
pdf(file = mypath, height = 7, width = 12)
heatmap.2(
x=X0,
Rowv=TRUE, Colv=NA,
x = X0,
Rowv = TRUE, Colv = NA,
distfun = dist, hclustfun = hclust,
dendrogram = "row", cexCol = 0.8, cexRow = 0.9, scale = "none",
breaks=colormapbreaks, symbreaks=FALSE, colsep = even_columns, sepcolor="white", offsetCol = 0.1,
#zlim=c(-132,132),
breaks = colormapbreaks, symbreaks = FALSE, colsep = even_columns, sepcolor = "white", offsetCol = 0.1,
# zlim = c(-132,132),
xlab = "Type of Media", ylab = "Gene Name",
cellnote = round(X0,digits=0), notecex = 0.4, key=TRUE,
keysize=1, trace="none", density.info=c("none"), margins=c(10, 8),
na.color="red", col=brewer.pal(11,"PuOr"),
main=cluster,
labRow=as.character(cluster_data$Gene), labCol=colnames_edit, colRow=cluster_data$color2,RowSideColors=cluster_data$color)
cellnote = round(X0, digits = 0), notecex = 0.4, key = TRUE,
keysize = 1, trace = "none", density.info = c("none"), margins = c(10, 8),
na.color = "red", col = brewer.pal(11, "PuOr"),
main = cluster,
labRow = as.character(cluster_data$Gene), labCol = colnames_edit, colRow = cluster_data$color2, RowSideColors = cluster_data$color
)
dev.off()
}
}
# print(paste("FINISHED", "CLUSTER",cluster,sep=" "))
# print(paste("FINISHED", "CLUSTER",cluster,sep = " "))
}