various changes
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parent
2274f01f23
commit
6c6709e41e
6 changed files with 198 additions and 29 deletions
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@ -48,6 +48,11 @@ if (!require("shinyBS")) {
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library(shinyBS)
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}
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if (!require("shinydashboard")) {
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install.packages("shinydashboard", dependencies = TRUE)
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library(shinydashboard)
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}
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if (!require("gridExtra")) {
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install.packages("gridExtra", dependencies = TRUE)
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library(gridExtra)
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93
scripts/functions/bp_lineage_diversity.R
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93
scripts/functions/bp_lineage_diversity.R
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@ -0,0 +1,93 @@
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########################################
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# Lineage barplot
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# Lineage and nsSNP count barplot
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# Lineage Diversity barplot
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########################################
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lin_count_bp_diversity <- function( lf_data = lin_wf
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, x_categ = "sel_lineages"
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, y_count = "snp_diversity"
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#, bar_fill_categ = "count_categ"
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, display_label_col = "snp_diversity_f"
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, bar_stat_stype = "identity"
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, x_lab_angle = 90
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, d_lab_size = 5
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, d_lab_hjust = 0.5
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, d_lab_vjust = 0.5
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, d_lab_col = "black"
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, my_xats = 20 # x axis text size
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, my_yats = 20 # y axis text size
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, my_xals = 22 # x axis label size
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, my_yals = 22 # y axis label size
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, my_lls = 22 # legend label size
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, bar_col_labels = c("Mutations", "Total Samples")
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, bar_col_values = c("grey50", "gray75")
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, bar_leg_name = ""
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, leg_location = "top"
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, y_log10 = FALSE
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, y_scale_percent = FALSE
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#, y_label = c("Count", "SNP diversity")
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, y_label = c("SNP diversity")
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) {
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g = ggplot(lf_data
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, aes( x = factor( eval(parse(text = x_categ)), ordered = T )
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, y = eval(parse(text = y_count))
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#, fill = eval(parse(text = bar_fill_categ))
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) )
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OutPlot = g + geom_bar( stat = bar_stat_stype
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, position = position_stack(reverse = TRUE)
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#, alpha = 1
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#, colour = "grey75"
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) +
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theme(axis.text.x = element_text(size = my_xats
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, angle = x_lab_angle)
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, axis.text.y = element_text(size = my_yats
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, angle = 90
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, hjust = 1
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, vjust = 0)
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, axis.title.x = element_text(size = my_xals
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, colour = "black")
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, axis.title.y = element_text(size = my_yals
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, colour = "black")
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, legend.position = leg_location
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, legend.text = element_text(size = my_lls)) +
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geom_label(aes(label = eval(parse(text = display_label_col)))
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, size = d_lab_size
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, hjust = d_lab_hjust
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, vjust = d_lab_vjust
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, colour = d_lab_col
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, show.legend = FALSE
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#, check_overlap = TRUE
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, position = position_stack(reverse = T)) +
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scale_fill_manual(values = bar_col_values
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, name = bar_leg_name
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, labels = bar_col_labels) +
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labs(title = ""
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, x = ""
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, y = y_label
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, colour = "black")
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if (y_log10){
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OutPlot = OutPlot +
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scale_y_continuous(trans = "log10"
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, labels = trans_format("log10", math_format(10^.x) ) )
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}
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if (y_scale_percent){
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OutPlot = OutPlot +
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scale_y_continuous(labels = scales::percent_format(accuracy = 1)) +
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#scale_y_continuous(labels = scales::percent) +
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labs(title = ""
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, x = ""
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, y = y_label
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, colour = "black")
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}
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return(OutPlot)
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}
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@ -28,6 +28,8 @@ wideP_consurf <- function(plotdf
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, "1": "Variable"
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, "2", "3", "4", "5", "6", "7", "8"
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, "9": "Conserved")
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, panel_col = "black"
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, panel_col_fill = "black"
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# axes title and label sizes
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, x_axls = 12 # x-axis label size
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@ -38,6 +40,7 @@ wideP_consurf <- function(plotdf
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, ptitle = ""
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, xlab = ""
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, ylab = ""
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, pts = 20
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# plot margins
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, t_margin = 0.5
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@ -282,9 +285,11 @@ wideP_consurf <- function(plotdf
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, vjust = 0)
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, axis.title.x = element_text(size = x_axls)
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, axis.title.y = element_text(size = y_axls )
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, panel.background = element_rect(fill = "black", color = "black")
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, panel.background = element_rect(fill = panel_col_fill, color = panel_col)
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, panel.grid.major = element_line(color = "black")
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, panel.grid.minor = element_line(color = "black")
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, plot.title = element_text(size = pts
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, hjust = 0.5)
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, plot.margin = margin(t = t_margin
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, r = r_margin
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, b = b_margin
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@ -400,8 +405,6 @@ wideP_consurf <- function(plotdf
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out = g1
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}
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#####################################################
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# #============================================
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# # x-axis: geom_tiles ~ ligand distance
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@ -548,13 +551,13 @@ wideP_consurf <- function(plotdf
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, legend2
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, ncol = 1
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, align = "hv"
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, rel_heights = c(3/4,1))
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, rel_heights = c(2/4,3/4))
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out2 = cowplot::plot_grid( out + theme(legend.position = "none")
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, legs
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, ncol = 2
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, align = "hv"
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, rel_widths = c(9/10, 0.5/10)
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, rel_widths = c(9/10, 0.4/10)
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)
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}else{
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out2 = cowplot::plot_grid( out + theme(legend.position = "none")
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63
scripts/functions/tests/data_for_testingF.R
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63
scripts/functions/tests/data_for_testingF.R
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@ -0,0 +1,63 @@
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############################################################################
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# merged_df3 = read.csv("~/git/Data/cycloserine/output/alr_all_params.csv"); source("~/git/LSHTM_analysis/config/alr.R")
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# if ( tolower(gene) == "alr") {
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# aa_pos_lig1 = NULL
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# aa_pos_lig2 = NULL
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# aa_pos_lig3 = NULL
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# p_title = gene
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# }
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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###########################################################################
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# merged_df3 = read.csv("~/git/Data/ethambutol/output/embb_all_params.csv"); source("~/git/LSHTM_analysis/config/embb.R")
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# if ( tolower(gene) == "embb") {
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# aa_pos_lig1 = aa_pos_ca
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# aa_pos_lig2 = aa_pos_cdl
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# aa_pos_lig3 = aa_pos_dsl
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# p_title = gene
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# }
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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###########################################################################
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merged_df3 = read.csv("~/git/Data/streptomycin/output/gid_all_params.csv")
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source("~/git/LSHTM_analysis/config/gid.R")
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if ( tolower(gene) == "gid") {
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aa_pos_lig1 = aa_pos_rna
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aa_pos_lig2 = aa_pos_sam
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aa_pos_lig3 = aa_pos_amp
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p_title = gene
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}
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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###########################################################################
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# merged_df3 = read.csv("~/git/Data/isoniazid/output/katg_all_params.csv"); source("~/git/LSHTM_analysis/config/katg.R")
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# if ( tolower(gene) == "katg") {
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# aa_pos_lig1 = aa_pos_hem
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# aa_pos_lig2 = NULL
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# aa_pos_lig3 = NULL
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# p_title = gene
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# }
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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###########################################################################
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# merged_df3 = read.csv("~/git/Data/pyrazinamide/output/pnca_all_params.csv"); source("~/git/LSHTM_analysis/config/pnca.R")
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# if ( tolower(gene) == "pnca") {
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# aa_pos_lig1 = aa_pos_fe
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# aa_pos_lig2 = NULL
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# aa_pos_lig3 = NULL
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# p_title = gene
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# }
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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###########################################################################
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merged_df3 = read.csv("~/git/Data/rifampicin/output/rpob_all_params.csv"); source("~/git/LSHTM_analysis/config/rpob.R")
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if ( tolower(gene) == "rpob") {
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aa_pos_lig1 = NULL
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aa_pos_lig2 = NULL
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aa_pos_lig3 = NULL
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p_title = gene
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}
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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#########################################################################
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@ -15,13 +15,13 @@ source("~/git/LSHTM_analysis/scripts/functions/consurfP.R")
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# p_title = gene
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# }
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###########################################################################
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merged_df3 = read.csv("~/git/Data/ethambutol/output/embb_all_params.csv"); source("~/git/LSHTM_analysis/config/embb.R")
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if ( tolower(gene) == "embb") {
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aa_pos_lig1 = aa_pos_ca
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aa_pos_lig2 = aa_pos_cdl
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aa_pos_lig3 = aa_pos_dsl
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p_title = gene
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}
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# merged_df3 = read.csv("~/git/Data/ethambutol/output/embb_all_params.csv"); source("~/git/LSHTM_analysis/config/embb.R")
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# if ( tolower(gene) == "embb") {
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# aa_pos_lig1 = aa_pos_ca
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# aa_pos_lig2 = aa_pos_cdl
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# aa_pos_lig3 = aa_pos_dsl
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# p_title = gene
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# }
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###########################################################################
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# merged_df3 = read.csv("~/git/Data/streptomycin/output/gid_all_params.csv"); source("~/git/LSHTM_analysis/config/gid.R")
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# if ( tolower(gene) == "gid") {
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# p_title = gene
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# }
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###########################################################################
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# merged_df3 = read.csv("~/git/Data/rifampicin/output/rpob_all_params.csv"); source("~/git/LSHTM_analysis/config/rpob.R")
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# if ( tolower(gene) == "rpob") {
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# aa_pos_lig1 = NULL
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# aa_pos_lig2 = NULL
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# aa_pos_lig3 = NULL
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# p_title = gene
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# }
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merged_df3 = read.csv("~/git/Data/rifampicin/output/rpob_all_params.csv"); source("~/git/LSHTM_analysis/config/rpob.R")
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if ( tolower(gene) == "rpob") {
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aa_pos_lig1 = NULL
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aa_pos_lig2 = NULL
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aa_pos_lig3 = NULL
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p_title = gene
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}
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#########################################################################
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consurf_palette1 = c("0" = "yellow2"
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@ -99,15 +99,19 @@ wideP_consurf(plotdf = merged_df3
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, "1" = "Variable"
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, "2", "3", "4", "5", "6", "7", "8"
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, "9" = "Conserved")
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, panel_col = "black"
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, panel_col_fill = "black"
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# axes title and label sizes
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, x_axts = 8
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, x_axts = 8
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, y_axts = 12
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, x_axls = 12
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, y_axls = 15
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, default_xtc = "black"
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, ptitle = p_title
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, xlab = ""
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, xlab = "" # ylab is above
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, pts = 20
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# x-axis: text colour
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, xtext_colour_aa = F
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@ -16,10 +16,10 @@ LP1<- LogoPlotCustomH (plot_df = merged_df3
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, x_axis_colname = "position"
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, y_axis_colname = "or_mychisq"
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, symbol_colname = "mutant_type"
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, y_axis_log = T
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, y_axis_log = F
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, log_value = log10
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, y_axis_increment = 100
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, rm_empty_y = T
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, y_axis_increment = 50
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, rm_empty_y = F
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, my_logo_col = 'chemistry'
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, x_lab = "Wild-type position"
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, y_lab = "Odds Ratio"
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@ -45,7 +45,7 @@ LP2<- LogoPlotSnps(plot_df = merged_df3
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, x_axis_colname = "position"
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, symbol_mut_colname = "mutant_type"
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, symbol_wt_colname = "wild_type"
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, omit_snp_count = c(1)# can be 0,1, 2, etc.# DD
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, omit_snp_count = c(0)# can be 0,1, 2, etc.# DD
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, my_logo_col = "chemistry" #DD
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, x_lab = "Wild-type position"
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, y_lab = "nsSNP count"
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# to select a small dataset: see test_ed_pfm_data.R
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#####################################################
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LP3<- LogoPlotMSA(msaSeq_mut = msa_seq
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, msaSeq_wt = wt_seq
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LP3<- LogoPlotMSA(unified_msa
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#msaSeq_mut = msa_seq
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#, msaSeq_wt = wt_seq
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, logo_type = c("EDLogo") # "EDLogo", bits_pfm", "probability_pfm", "bits_raw", "probability_raw")
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, EDScore_type = c("log")
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, bg_prob = NULL
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#, y_lab_mut
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, x_ats = 10
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, x_tangle = 90
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, y_ats = 15
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, y_ats = 12
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, y_tangle = 0
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, x_tts = 13
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, y_tts = 13
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@ -106,7 +107,7 @@ out_logoP = cowplot::plot_grid(LP3, LP1, LP2
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, nrow = 3
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, ncol = 1
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, rel_width = c(1/3, 0.5/3, 1/3)
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, rel_heights = c(1, 1, 1)
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, rel_heights = c(0.8/2, 0.5/2, 0.7/2)
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, align = "hv")
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out_logoP
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