checked logo_multiple_muts.R with the new sourcing script for data

scripts/plotting/corr_PS_LIG.R

@@ -249,5 +249,3 @@ dev.off()
 corr_lig_rho = corr.test(my_corr_lig[1:4], method = "spearman")$r
 corr_lig_p = corr.test(my_corr_lig[1:4], method = "spearman")$p
 #######################################################
-
-

scripts/plotting/get_plotting_dfs.R

@@ -110,9 +110,6 @@ cat("No. of rows in my_data:", nrow(logo_data)
 #=======================================================================
 #%% logo plots from dataframe
 
-#############
-# PLOTS
-#############
 foo = logo_data[, c("position"
                       , "mutant_type","duet_scaled", "or_mychisq"
                       , "mut_prop_polarity", "mut_prop_water")] 
@@ -150,6 +147,76 @@ rownames(wide_df_logor_m)
 colnames(wide_df_logor_m)
 
 position_logor = as.numeric(colnames(wide_df_logor_m))
+
+#===============================
+# logo data: multiple nsSNPs (>1)
+#=================================
+#require(data.table)
+
+# get freq count of positions so you can subset freq<1
+setDT(logo_data)[, mut_pos_occurrence := .N, by = .(position)] 
+
+table(logo_data$position)
+table(logo_data$mut_pos_occurrence)
+
+max_mut = max(table(logo_data$position))
+
+# extract freq_pos > 1
+my_data_snp = logo_data[logo_data$mut_pos_occurrence!=1,] 
+u = unique(my_data_snp$position)
+max_mult_mut = max(table(my_data_snp$position))
+
+if (nrow(my_data_snp) == nrow(logo_data) - table(logo_data$mut_pos_occurrence)[[1]] ){
+  
+  cat("PASS: positions with  multiple muts extracted"
+      , "\nNo. of mutations:", nrow(my_data_snp)
+      , "\nNo. of positions:", length(u)
+      , "\nMax no. of muts at any position", max_mult_mut)
+}else{
+  cat("FAIL: positions with multiple muts could NOT be extracted"
+      , "\nExpected:",nrow(logo_data) - table(logo_data$mut_pos_occurrence)[[1]]
+      , "\nGot:", nrow(my_data_snp) )
+}
+
+cat("\nNo. of sites with only 1 mutations:", table(logo_data$mut_pos_occurrence)[[1]])
+
+#--------------------------------------
+# matrix for_mychisq mutant type
+# frequency of mutant type by position
+#---------------------------------------
+table(my_data_snp$mutant_type, my_data_snp$position)
+tab_mt = table(my_data_snp$mutant_type, my_data_snp$position)
+class(tab_mt)
+
+# unclass to convert to matrix
+tab_mt = unclass(tab_mt)
+tab_mt = as.matrix(tab_mt, rownames = T)
+
+# should be TRUE
+is.matrix(tab_mt)
+
+rownames(tab_mt) #aa
+colnames(tab_mt) #pos
+
+#-------------------------------------
+# matrix for wild type
+# frequency of wild type by position
+#-------------------------------------
+tab_wt = table(my_data_snp$wild_type, my_data_snp$position); tab_wt
+tab_wt = unclass(tab_wt)
+
+# remove wt duplicates
+wt = my_data_snp[, c("position", "wild_type")]
+wt = wt[!duplicated(wt),]
+
+tab_wt = table(wt$wild_type, wt$position); tab_wt # should all be 1
+
+rownames(tab_wt)
+rownames(tab_wt)
+
+identical(colnames(tab_mt), colnames(tab_wt))
+identical(ncol(tab_mt), ncol(tab_wt))
+
 ########################################################################
 #                           End of script
 ########################################################################

scripts/plotting/logo_combined.R

@@ -3,95 +3,6 @@
 # TASK: producing logo-type plot showing
 # multiple muts per position coloured by aa property
 #########################################################
-#=======================================================================
-# working dir and loading libraries
-getwd()
-setwd("~/git/LSHTM_analysis/scripts/plotting")
-getwd()
-
-source("Header_TT.R")
-source("../functions/plotting_globals.R")
-source("../functions/plotting_data.R")
-source("../functions/combining_dfs_plotting.R")
-###########################################################
-# command line args
-#********************
-#drug = 'streptomycin'
-#gene = 'gid'
-#********************
-# !!!FUTURE TODO!!!
-# Can pass additional params of output/plot dir by user. 
-# Not strictly required for my workflow  since it is optimised
-# to have a streamlined input/output flow without filename worries.
-#********************
-spec = matrix(c(
-  "drug"       , "d",  1, "character",
-  "gene"       , "g",  1, "character",
-  "data_file1" , "fa", 2, "character",
-  "data_file2" , "fb", 2, "character" 
-), byrow = TRUE, ncol = 4)
-
-opt = getopt(spec)
-
-#FIXME: detect if script running from cmd, then set these
-drug            = opt$drug
-gene            = opt$gene
-infile_params   = opt$data_file1
-infile_metadata = opt$data_file2
-
-if(is.null(drug)|is.null(gene)) {
-  stop("Missing arguments: --drug and --gene must both be specified (case-sensitive)")
-}
-
-#===========
-# input
-#===========
-#---------------------
-# call: import_dirs()
-#---------------------
-import_dirs(drug_name = drug, gene_name = gene)
-
-#---------------------------
-# call: plotting_data()
-#---------------------------
-#if (!exists("infile_params") && exists("gene")){
-if (!is.character(infile_params) && exists("gene")){ # when running as cmd
-  #in_filename_params = paste0(tolower(gene), "_all_params.csv") 
-  in_filename_params = paste0(tolower(gene), "_comb_afor.csv") # part combined for gid
-  infile_params = paste0(outdir, "/", in_filename_params)
-  cat("\nInput file for mcsm comb data not specified, assuming filename: ", infile_params, "\n")
-}
-
-# Input 1: read <gene>_comb_afor.csv
-cat("\nReading mcsm combined data file: ", infile_params)
-mcsm_df = read.csv(infile_params, header = T)
-pd_df = plotting_data(mcsm_df)
-my_df_u       = pd_df[[2]]
-
-#--------------------------------
-# call: combining_dfs_plotting()
-#--------------------------------
-#if (!exists("infile_metadata") && exists("gene")){
-if (!is.character(infile_metadata) && exists("gene")){ # when running as cmd
-  in_filename_metadata = paste0(tolower(gene), "_metadata.csv") # part combined for gid
-  infile_metadata = paste0(outdir, "/", in_filename_metadata)
-  cat("\nInput file for gene metadata not specified, assuming filename: ", infile_metadata, "\n")
-}
-
-# Input 2: read <gene>_meta data.csv
-cat("\nReading meta data file: ", infile_metadata)
-
-gene_metadata <- read.csv(infile_metadata
-                          , stringsAsFactors = F
-                          , header = T)
-
-all_plot_dfs = combining_dfs_plotting(my_df_u
-                                      , gene_metadata
-                                      , lig_dist_colname = 'ligand_distance'
-                                      , lig_dist_cutoff = 10)
-
-merged_df3 = all_plot_dfs[[2]]
-
 #===========
 # output
 #===========

scripts/plotting/logo_multiple_muts.R

@@ -1,29 +1,9 @@
 #!/usr/bin/env Rscript
-#########################################################
-# TASK: producing logo-type plot showing
-# multiple muts per position coloured by aa property
-#########################################################
-#=======================================================================
-# working dir and loading libraries
 getwd()
 setwd("~/git/LSHTM_analysis/scripts/plotting")
 getwd()
-
 source("Header_TT.R")
-source("../functions/plotting_globals.R")
+
-source("../functions/plotting_data.R")
-source("../functions/combining_dfs_plotting.R")
-###########################################################
-# command line args
-#********************
-#drug = 'streptomycin'
-#gene = 'gid'
-#********************
-# !!!FUTURE TODO!!!
-# Can pass additional params of output/plot dir by user. 
-# Not strictly required for my workflow  since it is optimised
-# to have a streamlined input/output flow without filename worries.
-#********************
 spec = matrix(c(
   "drug"       , "d",  1, "character",
   "gene"       , "g",  1, "character",
@@ -33,7 +13,6 @@ spec = matrix(c(
 
 opt = getopt(spec)
 
-#FIXME: detect if script running from cmd, then set these
 drug            = opt$drug
 gene            = opt$gene
 infile_params   = opt$data_file1
@@ -42,131 +21,22 @@ infile_metadata = opt$data_file2
 if(is.null(drug)|is.null(gene)) {
   stop("Missing arguments: --drug and --gene must both be specified (case-sensitive)")
 }
+
 #===========
-# input
+# Input
 #===========
-#---------------------
-# call: import_dirs()
-#---------------------
-import_dirs(drug_name = drug, gene_name = gene)
 
-#---------------------------
+source("get_plotting_dfs.R")
-# call: plotting_data()
-#---------------------------
-#if (!exists("infile_params") && exists("gene")){
-if (!is.character(infile_params) && exists("gene")){ # when running as cmd
-  #in_filename_params = paste0(tolower(gene), "_all_params.csv") 
-  in_filename_params = paste0(tolower(gene), "_comb_afor.csv") # part combined for gid
-  infile_params = paste0(outdir, "/", in_filename_params)
-  cat("\nInput file for mcsm comb data not specified, assuming filename: ", infile_params, "\n")
-}
-
-# Input 1: read <gene>_comb_afor.csv
-cat("\nReading mcsm combined data file: ", infile_params)
-mcsm_df = read.csv(infile_params, header = T)
-pd_df = plotting_data(mcsm_df)
-my_df_u       = pd_df[[2]] # this forms one of the input for combining_dfs_plotting()
-
-#--------------------------------
-# call: combining_dfs_plotting()
-#--------------------------------
-#if (!exists("infile_metadata") && exists("gene")){
-if (!is.character(infile_metadata) && exists("gene")){ # when running as cmd
-  in_filename_metadata = paste0(tolower(gene), "_metadata.csv") # part combined for gid
-  infile_metadata = paste0(outdir, "/", in_filename_metadata)
-  cat("\nInput file for gene metadata not specified, assuming filename: ", infile_metadata, "\n")
-}
-
-# Input 2: read <gene>_meta data.csv
-cat("\nReading meta data file: ", infile_metadata)
-
-gene_metadata <- read.csv(infile_metadata
-                          , stringsAsFactors = F
-                          , header = T)
-
-all_plot_dfs = combining_dfs_plotting(my_df_u
-                                      , gene_metadata
-                                      , lig_dist_colname = 'ligand_distance'
-                                      , lig_dist_cutoff = 10)
-
-merged_df3 = all_plot_dfs[[2]]
 
 #===========
 # output
 #===========
-
 logo_multiple_muts = "logo_multiple_muts.svg"
 plot_logo_multiple_muts = paste0(plotdir,"/", logo_multiple_muts)
 
-##########################################################################
+#*********************
-
-#%%%%%%%%%%%%%%%%%%%%%%%%%%%%
-# REASSIGNMENT
-my_df = merged_df3
-#%%%%%%%%%%%%%%%%%%%%%%%%%%%%
-
-colnames(my_df)
-str(my_df)
-
-#rownames(my_df) = my_df$mutation
-
-c1 = unique(my_df$position) 
-nrow(my_df) 
-
-# get freq count of positions so you can subset freq<1
-#require(data.table)
-setDT(my_df)[, mut_pos_occurrence := .N, by = .(position)] #189, 36
-
-table(my_df$position)
-table(my_df$mut_pos_occurrence)
-
-max_mut = max(table(my_df$position))
-
-# extract freq_pos>1
-my_data_snp = my_df[my_df$mut_pos_occurrence!=1,] 
-u = unique(my_data_snp$position)
-max_mult_mut = max(table(my_data_snp$position))
-
-if (nrow(my_data_snp) == nrow(my_df) - table(my_df$mut_pos_occurrence)[[1]] ){
-  
-  cat("PASS: positions with  multiple muts extracted"
-      , "\nNo. of mutations:", nrow(my_data_snp)
-      , "\nNo. of positions:", length(u)
-      , "\nMax no. of muts at any position", max_mult_mut)
-}else{
-  cat("FAIL: positions with multiple muts could NOT be extracted"
-      , "\nExpected:",nrow(my_df) - table(my_df$mut_pos_occurrence)[[1]]
-      , "\nGot:", nrow(my_data_snp) )
-}
-
-cat("\nNo. of sites with only 1 mutations:", table(my_df$mut_pos_occurrence)[[1]])
-
-
-########################################################################
-#               end of data extraction and cleaning for_mychisq plots          #
-########################################################################
-
-#==============
-# matrix for_mychisq mutant type
-# frequency of mutant type by position
-#==============
-table(my_data_snp$mutant_type, my_data_snp$position)
-tab_mt = table(my_data_snp$mutant_type, my_data_snp$position)
-class(tab_mt)
-
-# unclass to convert to matrix
-tab_mt = unclass(tab_mt)
-tab_mt = as.matrix(tab_mt, rownames = T)
-
-#should be TRUE
-is.matrix(tab_mt)
-
-rownames(tab_mt) #aa
-colnames(tab_mt) #pos
-
-#**************
 # Plot 1: mutant logo
-#**************
+#*********************
 p0 = ggseqlogo(tab_mt
                , method = 'custom'
                , seq_type = 'aa') + 
@@ -179,40 +49,21 @@ p0 = ggseqlogo(tab_mt
   scale_y_continuous( breaks = 1:max_mult_mut
                       , limits = c(0, max_mult_mut))
 
-#p0
+p0
+cat('\nDone: p0')
 
-cat('p0 done\n')
 # further customisation
-p1 = p0 + theme(legend.position = "none"
+mut_logo_p = p0 + theme(legend.position = "none"
                         , legend.title = element_blank()
                         , legend.text = element_text(size = 20)
                         , axis.text.x = element_text(size = 17, angle = 90)
                         , axis.text.y = element_blank())
-#p1
+#mut_logo_p
-cat('p0+p1 done\n')
+cat('\nDone: p0+mut_logo_p')
-#==============
-# matrix for wild type
-# frequency of wild type by position
-#==============  
-tab_wt = table(my_data_snp$wild_type, my_data_snp$position); tab_wt
-tab_wt = unclass(tab_wt)
 
-#remove wt duplicates
+#***********************
-wt = my_data_snp[, c("position", "wild_type")]
-wt = wt[!duplicated(wt),]
-
-tab_wt = table(wt$wild_type, wt$position); tab_wt # should all be 1
-rownames(tab_wt)
-rownames(tab_wt)
-
-#**************
 # Plot 2: wild_type logo
-#**************
+#***********************
-# sanity check: MUST BE TRUE
-
-identical(colnames(tab_mt), colnames(tab_wt))
-identical(ncol(tab_mt), ncol(tab_wt))
-
 p2 = ggseqlogo(tab_wt
                , method = 'custom'
                , seq_type = 'aa'
@@ -227,10 +78,10 @@ p2 = ggseqlogo(tab_wt
   scale_x_continuous(breaks = 1:ncol(tab_wt)
                      , labels = colnames(tab_wt)) 
 #p2
+cat('\nDone: p2 done')
 
 # further customise
-cat('p2 done\n')
+wt_logo_p = p2 +
-p3 = p2 +
   theme(legend.position = "bottom"
         #, legend.title = element_blank()
         , legend.title = element_text("Amino acid properties", size = 20)
@@ -241,27 +92,27 @@ p3 = p2 +
   
   labs(x= "Position")
 
-#p3
+#wt_logo_p
+cat('\nDone: wt_logo_p')
 
-# Now combine using cowplot, which ensures the plots are aligned
+#------------------------------------
-suppressMessages( require(cowplot) )
+# Now combine using cowplot
+# which ensures the plots are aligned
+#------------------------------------
+#suppressMessages( require(cowplot) )
+cat('\nDone: wt_logo_p')
 
-cat('p3 done\n')
+#plot_grid(p1, p3, ncol = 1, align = 'v') 
-
+cat('\nDone: mut_logo_p + wt_logo_p')
-#plot_grid(p1, p3, ncol = 1, align = 'v') #+ 
-cat('p3+p2 done\n')
-
-#colour scheme
-#https://rdrr.io/cran/ggseqlogo/src/R/col_schemes.r
-
-cat("Output plot:", plot_logo_multiple_muts, "\n")
 
+# colour scheme: https://rdrr.io/cran/ggseqlogo/src/R/col_schemes.r
+cat("\nOutput plot:", plot_logo_multiple_muts, "\n")
 svg(plot_logo_multiple_muts, width = 32, height = 10)
 
-OutPlot1 = cowplot::plot_grid(p1, p3
+mult_muts_combined = cowplot::plot_grid(mut_logo_p, wt_logo_p
                                         , nrow = 2
                                         , align = "v"
                                         , rel_heights = c(3/4, 1/4))
 
-print(OutPlot1)
+print(mult_muts_combined)
 #dev.off()

scripts/plotting/logo_plot.R

@@ -77,7 +77,7 @@ dev.off()
 cat("Logo plot with log10 OR as y axis:", plot_logo_logOR)
 svg(plot_logo_logOR, width = 30 , height = 6)
 
-ggseqlogo(wide_df_logor_m
+logo_logOR = ggseqlogo(wide_df_logor_m
           , method = "custom"
           , seq_type="aa") + ylab("my custom height") +
   theme(legend.position = "bottom"
@@ -97,7 +97,10 @@ ggseqlogo(wide_df_logor_m
                    , limits = factor(1:length(position_logor)))+
   ylab("Log (Odds Ratio)") + 
   scale_y_continuous(limits = c(0, 9))
+
+print(logo_logOR)
 dev.off()
+
 ######################################################################=
 #                             End of script
 ######################################################################=

scripts/plotting/running_plotting_scripts.txt

@@ -29,9 +29,7 @@ sources:
 ./logo_plot.R -d streptomycin -g gid
 
 sources:
- ## plotting_globals.R (previously dir.R)
+ ## get_plotting_dfs.R
- ## plotting_data.R 
- ## combining_dfs_plotting.R
 
  outputs: plotdir
  ## 1 svg of OR for all positions
@@ -46,9 +44,7 @@ sources:
 ./logo_multiple_muts.R -d streptomycin -g gid
 
 sources:
- ## plotting_globals.R (previously dir.R)
+ ## get_plotting_dfs.R
- ## plotting_data.R 
- ## combining_dfs_plotting.R
 
  outputs: plotdir
  ## 1 svg of multiple muts for all positions > 1 muts (mutations + wt)
@@ -63,9 +59,7 @@ sources:
 #========================
 
 sources:
- ## plotting_globals.R (previously dir.R)
+ ## get_plotting_dfs.R
- ## plotting_data.R 
- ## combining_dfs_plotting.R
 
  outputs: plotdir
  ## 1 svg combined of OR logo plot + mulitple_muts i.e output from