updating script to sort out proper merging for plotting
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1 changed files with 121 additions and 30 deletions
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@ -23,40 +23,91 @@ getwd()
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setwd("~/git/LSHTM_analysis/scripts/plotting/")
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getwd()
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require("getopt", quietly = TRUE) # cmd parse arguments
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# load functions
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source("Header_TT.R")
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#require(data.table)
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#require(arsenal)
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#require(compare)
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#library(tidyverse)
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source("plotting_data.R")
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source("../functions/plotting_globals.R")
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source("../functions/plotting_data.R")
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# should return the following dfs, directories and variables
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# my_df
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# my_df_u
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# my_df_u_lig
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# dup_muts
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#############################################################
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# command line args
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#********************
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# !!!FUTURE TODO!!!
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# Can pass additional params of output/plot dir by user.
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# Not strictly required for my workflow since it is optimised
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# to have a streamlined input/output flow without filename worries.
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#********************
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spec = matrix(c(
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"drug" ,"d", 1, "character",
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"gene" ,"g", 1, "character",
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"data" ,"f", 2, "character"
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), byrow = TRUE, ncol = 4)
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cat("Directories imported:"
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, "\n===================="
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, "\ndatadir:", datadir
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, "\nindir:", indir
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, "\noutdir:", outdir
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, "\nplotdir:", plotdir)
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opt = getopt(spec)
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cat("Variables imported:"
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, "\n====================="
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, "\ndrug:", drug
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, "\ngene:", gene
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, "\ngene_match:", gene_match
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, "\nAngstrom symbol:", angstroms_symbol
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, "\nNo. of duplicated muts:", dup_muts_nu
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, "\ndr_muts_col:", dr_muts_col
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, "\nother_muts_col:", other_muts_col
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, "\ndrtype_col:", resistance_col)
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#FIXME: detect if script running from cmd, then set these
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drug = opt$drug
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gene = opt$gene
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infile = opt$data
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# hardcoding when not using cmd
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#drug = "streptomycin"
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#gene = "gid"
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# clear excess variable
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rm(my_df, upos, dup_muts)
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if(is.null(drug)|is.null(gene)) {
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stop("Missing arguments: --drug and --gene must both be specified (case-sensitive)")
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}
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#########################################################
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# call functions with relevant args
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#***********************************
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# import_dirs(): returns
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# datadir
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# indir
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# outdir
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# plotdir
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# dr_muts_col
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# other_muts_col
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# resistance_col
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#***********************************
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import_dirs(drug, gene)
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#***********************************
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# plotting_data(): returns
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# my_df
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# my_df_u
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# my_df_u_lig
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# dup_muts
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#***********************************
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#infile = "/home/tanu/git/Data/streptomycin/output/gid_comb_stab_struc_params.csv"
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if (!exists("infile") && exists("gene")){
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#if (!is.character(infile) && exists("gene")){
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#in_filename_params = paste0(tolower(gene), "_all_params.csv")
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#in_filename_params = paste0(tolower(gene), "_comb_stab_struc_params.csv") # part combined for gid
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in_filename_params = paste0(tolower(gene), "_comb_afor.csv") # part combined for gid
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infile = paste0(outdir, "/", in_filename_params)
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cat("\nInput file not specified, assuming filename: ", infile, "\n")
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}
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# Get the DFs out of plotting_data()
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pd_df = plotting_data(infile)
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my_df = pd_df[[1]]
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my_df_u = pd_df[[2]]
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my_df_u_lig = pd_df[[3]]
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dup_muts = pd_df[[4]]
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cat(paste0("Directories imported:"
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, "\ndatadir:" , datadir
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, "\nindir:" , indir
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, "\noutdir:" , outdir
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, "\nplotdir:" , plotdir))
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cat(paste0("\nVariables imported:"
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, "\ndrug:" , drug
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, "\ngene:" , gene
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, "\ngene match:" , gene_match
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, "\n"))
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#========================================================
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#===========
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# input
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@ -102,7 +153,6 @@ cat("Dim:", dim(gene_metadata))
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table(gene_metadata$mutation_info)
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# counting NAs in AF, OR cols
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# or_mychisq
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if (identical(sum(is.na(my_df_u$or_mychisq))
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@ -157,6 +207,10 @@ cat(paste0("Merging dfs with NAs: big df (1-many relationship b/w id & mut)"
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, "\nMerging columns identified:"))
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print(merging_cols)
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# using all common cols create confusion, so pick one!
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# merging_cols = merging_cols[[1]]
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merging_cols = 'mutationinformation'
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# important checks!
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table(nchar(my_df_u$mutationinformation))
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table(nchar(my_df_u$wild_type))
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@ -170,6 +224,43 @@ merged_df2 = merge(x = gene_metadata
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, all.y = T)
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cat("Dim of merged_df2: ", dim(merged_df2))
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dup_cols = names(merged_df2)[grepl("\\.x$|\\.y$", names(merged_df2))]
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cat("\nNo. of duplicate cols:", length(dup_cols))
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check_df_cols = merged_df2[dup_cols]
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identical(check_df_cols$wild_type.x, check_df_cols$wild_type.y)
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identical(check_df_cols$position.x, check_df_cols$position.y)
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identical(check_df_cols$mutant_type.x, check_df_cols$mutant_type.y)
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# False: because some of the ones with OR don't have mutation
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identical(check_df_cols$mutation.x, check_df_cols$mutation.y)
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cols_to_drop = names(merged_df2)[grepl("\\.y",names(merged_df2))]
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cat("\nNo. of cols to drop:", length(cols_to_drop))
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# subset
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merged_df2 = merged_df2[,!(names(merged_df2)%in%cols_to_drop)]
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# rename the cols with '.x' suffix
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names(merged_df2)[grepl("\\.x$|\\.y$", names(merged_df2))]
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colnames(merged_df2) <- gsub("\\.x$", "", colnames(merged_df2))
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names(merged_df2)[grepl("\\.x$|\\.y$", names(merged_df2))]
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#======================================================
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#-------------
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# DEBUG
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#-------------
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merged_df2_g = merged_df2[,!(names(merged_df2)%in%cols_to_drop)]
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check_cols = colnames(merged_df2)[!colnames(merged_df2)%in%colnames(merged_df2_g)]
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if ( identical(check_cols, cols_to_drop) ){
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cat("\nPASS: cols identified have been successfully dropped"
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, "\nNo. of cols dropped: ", length(check_cols)
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, "\nNo. of cols in original df: ", ncol(merged_df2)
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, "\nNo. of cols in revised df: " , ncol(merged_df2_g))
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}
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#======================================================
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head(merged_df2$position)
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# sanity check
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@ -185,7 +276,7 @@ if(nrow(gene_metadata) == nrow(merged_df2)){
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, "\nFinding discrepancy")
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merged_muts_u = unique(merged_df2$mutationinformation)
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meta_muts_u = unique(gene_metadata$mutationinformation)
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# find the index where it differs
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# find the index where it differs
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unique(meta_muts_u[! meta_muts_u %in% merged_muts_u])
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quit()
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}
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