@sjcrh/proteinpaint-server 2.29.1 → 2.29.2

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package/utils/edge.R ADDED
@@ -0,0 +1,86 @@
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+ # json='{"case":"SJMB066856,SJMB069601,SJMB030827,SJMB030838,SJMB031131,SJMB031227,SJMB077221,SJMB077223","control":"SJMB069596,SJMB069587,SJMB074736,SJMB030488,SJMB030825,SJMB031110,SJMB032998,SJMB033002","input_file":"/Users/rpaul1/pp_data/files/hg38/sjmb12/rnaseq/geneCounts.txt"}' && time echo $json | Rscript edge.R
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+
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+ # json='{"case":"SJMB030827,SJMB030838,SJMB064540,SJMB064538,SJMB064520,SJMB064535,SJMB031131,SJMB031227","control":"SJMB030488,SJMB030825,SJMB064537,SJMB064510,SJMB064533,SJMB064534,SJMB031110","input_file":"/Users/rpaul1/pp_data/files/hg38/sjmb12/rnaseq/geneCounts.txt"}' && time echo $json | Rscript edge.R
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+
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+ # Checking if all R packages are installed or not, if not installing each one of them
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+
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+ jsonlite_path <- system.file(package='jsonlite')
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+ if (nchar(jsonlite_path) == 0) {
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+ install.packages("jsonlite", repos='https://cran.case.edu/')
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+ }
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+
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+ edgeR_path <- system.file(package='edgeR')
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+ if (nchar(edgeR_path) == 0) {
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+ BiocManager::install("edgeR")
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+ }
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+
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+ readr_path <- system.file(package='readr')
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+ if (nchar(readr_path) == 0) {
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+ install.packages("readr", repos='https://cran.case.edu/')
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+ }
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+
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+
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+ library(jsonlite)
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+ library(stringr)
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+ library(readr)
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+ suppressWarnings({
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+ suppressPackageStartupMessages(library(edgeR))
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+ suppressPackageStartupMessages(library(dplyr))
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+ })
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+
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+ infile <- file("stdin")
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+ input <- fromJSON(infile)
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+ print (input$output_path)
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+ cases <- unlist(strsplit(input$case, ","))
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+ controls <- unlist(strsplit(input$control, ","))
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+ combined <- c("geneID","geneSymbol",cases,controls)
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+ #data %>% select(all_of(combined))
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+ read_file_time_start <- Sys.time()
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+ read_counts <- read_tsv(input$input_file, col_names = TRUE, col_select = combined)
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+ geneIDs <- unlist(read_counts[1])
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+ geneSymbols <- unlist(read_counts[2])
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+ read_counts <- select(read_counts, -geneID)
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+ read_counts <- select(read_counts, -geneSymbol)
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+ read_file_time_stop <- Sys.time()
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+ print (read_file_time_stop - read_file_time_start)
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+
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+ diseased <- rep("Diseased", length(cases))
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+ control <- rep("Control", length(controls))
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+ conditions <- c(diseased, control)
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+ tabs <- rep("\t",length(geneIDs))
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+ gene_id_symbols <- paste0(geneIDs,tabs,geneSymbols)
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+ y <- DGEList(counts = as.matrix(read_counts), group = conditions, genes = gene_id_symbols)
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+ keep <- filterByExpr(y)
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+ y <- y[keep, keep.lib.sizes = FALSE]
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+ y <- calcNormFactors(y, method = "TMM")
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+ #print (y)
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+ calculate_DE_time_start <- Sys.time()
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+ dge <- estimateDisp(y = y)
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+ et <- exactTest(object = dge)
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+ calculate_DE_time_stop <- Sys.time()
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+ print ("Time to calculate DE")
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+ print (calculate_DE_time_stop - calculate_DE_time_start)
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+ #print (et)
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+ logfc <- et$table$logFC
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+ logcpm <- et$table$logCPM
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+ pvalues <- et$table$PValue
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+ genes_matrix <- str_split_fixed(unlist(et$genes),"\t",2)
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+ geneids <- unlist(genes_matrix[,1])
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+ genesymbols <- unlist(genes_matrix[,2])
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+ adjust_p_values <- p.adjust(pvalues, method = "fdr")
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+
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+ output <- data.frame(geneids,genesymbols,logfc,-log10(pvalues),-log10(adjust_p_values))
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+ names(output)[1] <- "gene_name"
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+ names(output)[2] <- "gene_symbol"
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+ names(output)[3] <- "fold_change"
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+ names(output)[4] <- "original_p_value"
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+ names(output)[5] <- "adjusted_p_value"
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+
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+ output_json <- toJSON(output)
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+ print ("output_json")
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+ output_file <- paste0(input$output_path,"/r_output.txt")
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+ print (output_file)
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+ cat(output_json, file = output_file)
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+ #top_degs = topTags(object = et, n = "Inf")
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+ #print ("top_degs")
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+ #print (top_degs)