From 78220da9026c4c2d2e17e14ecbe6be6dfd57a37f Mon Sep 17 00:00:00 2001 From: runjin326 <47674661+runjin326@users.noreply.github.com> Date: Fri, 22 Oct 2021 20:21:18 -0400 Subject: [PATCH] Oncoprint output count tables (#1191) --- .../oncoprint-landscape/01-map-to-sample_id.R | 2 +- .../oncoprint-landscape/02-plot-oncoprint.R | 26 +- .../03-oncoprint-n-count-table.R | 236 ++++++++++++++++++ analyses/oncoprint-landscape/README.md | 8 +- analyses/oncoprint-landscape/run-oncoprint.sh | 22 +- ...ary-plus_embryonal_oncoprint_summary_n.tsv | 48 ++++ .../primary-plus_hgat_oncoprint_summary_n.tsv | 84 +++++++ .../primary-plus_lgat_oncoprint_summary_n.tsv | 23 ++ .../primary-plus_n_per_cancer_group.tsv | 0 ...primary-plus_other_oncoprint_summary_n.tsv | 44 ++++ ...ary_only_embryonal_oncoprint_summary_n.tsv | 45 ++++ .../primary_only_hgat_oncoprint_summary_n.tsv | 82 ++++++ .../primary_only_lgat_oncoprint_summary_n.tsv | 23 ++ .../primary_only_n_per_cancer_group.tsv | 0 ...primary_only_other_oncoprint_summary_n.tsv | 40 +++ .../tables/sample_n_in_oncoprint.tsv | 9 + 16 files changed, 681 insertions(+), 11 deletions(-) create mode 100644 analyses/oncoprint-landscape/03-oncoprint-n-count-table.R create mode 100644 analyses/oncoprint-landscape/tables/primary-plus_embryonal_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/primary-plus_hgat_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/primary-plus_lgat_oncoprint_summary_n.tsv rename analyses/oncoprint-landscape/{data => tables}/primary-plus_n_per_cancer_group.tsv (100%) create mode 100644 analyses/oncoprint-landscape/tables/primary-plus_other_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/primary_only_embryonal_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/primary_only_hgat_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/primary_only_lgat_oncoprint_summary_n.tsv rename analyses/oncoprint-landscape/{data => tables}/primary_only_n_per_cancer_group.tsv (100%) create mode 100644 analyses/oncoprint-landscape/tables/primary_only_other_oncoprint_summary_n.tsv create mode 100644 analyses/oncoprint-landscape/tables/sample_n_in_oncoprint.tsv diff --git a/analyses/oncoprint-landscape/01-map-to-sample_id.R b/analyses/oncoprint-landscape/01-map-to-sample_id.R index f66d0ba3ff..27da3630e7 100644 --- a/analyses/oncoprint-landscape/01-map-to-sample_id.R +++ b/analyses/oncoprint-landscape/01-map-to-sample_id.R @@ -387,7 +387,7 @@ gather_n_per_cancer_group <- function(metadata, broad_histology){ } } -output_file <- file.path('data', paste0(opt$filename_lead, "_n_per_cancer_group.tsv")) +output_file <- file.path('tables', paste0(opt$filename_lead, "_n_per_cancer_group.tsv")) lapply(as.list(c("Low-grade astrocytic tumor","Embryonal tumor", "Diffuse astrocytic and oligodendroglial tumor", "Other CNS")), function(x) gather_n_per_cancer_group(histologies_df,x)) %>% diff --git a/analyses/oncoprint-landscape/02-plot-oncoprint.R b/analyses/oncoprint-landscape/02-plot-oncoprint.R index f6ee9bdf87..8d21c34e38 100644 --- a/analyses/oncoprint-landscape/02-plot-oncoprint.R +++ b/analyses/oncoprint-landscape/02-plot-oncoprint.R @@ -43,6 +43,14 @@ if (!dir.exists(plots_dir)) { dir.create(plots_dir) } +# Path to output directory for tables produced +tables_dir <- + file.path(root_dir, "analyses", "oncoprint-landscape", "tables") + +if (!dir.exists(tables_dir)) { + dir.create(tables_dir) +} + # Source the custom functions script source( file.path( @@ -112,6 +120,12 @@ option_list <- list( action = "store_true", default = FALSE, help = "logical statement on whether to include intronic variants in oncoprint plot" + ), + optparse::make_option( + c("--output_table"), + type = "character", + default = NULL, + help = "file name for the output tables" ) ) @@ -269,22 +283,26 @@ if (!is.null(opt$goi_list)){ # Get top mutated genes per this subset object gene_sum <- mafSummary(filtered_maf_object)$gene.summary + # write out results + if (!is.null(opt$output_table)) { + readr::write_tsv(gene_sum, file.path("tables", opt$output_table)) + } + # Sort to get top altered genes rather than mutated only genes goi_list <- gene_sum %>% dplyr::arrange(dplyr::desc(AlteredSamples)) %>% # Filter to genes where multiple samples have an alteration dplyr::filter(AlteredSamples > 1) %>% dplyr::pull(Hugo_Symbol) - + if (opt$top_n < length(goi_list)) { # Now let's filter to the `top_n` genes goi_list <- goi_list[1:opt$top_n] - + } - } -#### Plot and Save Oncoprint -------------------------------------------------- +### Plot and Save Oncoprint -------------------------------------------------- # Given a maf object, plot an oncoprint of the variants in the # dataset and save as a png file. diff --git a/analyses/oncoprint-landscape/03-oncoprint-n-count-table.R b/analyses/oncoprint-landscape/03-oncoprint-n-count-table.R new file mode 100644 index 0000000000..082bdf7355 --- /dev/null +++ b/analyses/oncoprint-landscape/03-oncoprint-n-count-table.R @@ -0,0 +1,236 @@ +# This script outputs the oncoprint N counts table + +#### Set Up -------------------------------------------------------------------- + +# Load libraries +library(dplyr) +library(maftools) + +# Get `magrittr` pipe +`%>%` <- dplyr::`%>%` + +#### Directories and Files ----------------------------------------------------- + +# Detect the ".git" folder -- this will in the project root directory. +# Use this as the root directory to ensure proper execution, no matter where +# it is called from. +root_dir <- rprojroot::find_root(rprojroot::has_dir(".git")) + +# Path to output directory for table produced +results_dir <- + file.path(root_dir, "analyses", "oncoprint-landscape", "tables") + +if (!dir.exists(results_dir)) { + dir.create(results_dir) +} + +#### Command line options ------------------------------------------------------ + +# Declare command line options +option_list <- list( + optparse::make_option( + c("-m", "--maf_file_po"), + type = "character", + default = NULL, + help = "file path to MAF file that contains SNV information of primary_only samples", + ), + optparse::make_option( + c("-c", "--cnv_file_po"), + type = "character", + default = NULL, + help = "file path to file that contains CNV information of primary_only samples" + ), + optparse::make_option( + c("-f", "--fusion_file_po"), + type = "character", + default = NULL, + help = "file path to file that contains fusion information of primary_only samples" + ), + optparse::make_option( + c("-g", "--maf_file_pp"), + type = "character", + default = NULL, + help = "file path to MAF file that contains SNV information of primary-plus samples", + ), + optparse::make_option( + c("-d", "--cnv_file_pp"), + type = "character", + default = NULL, + help = "file path to file that contains CNV information of primary-plus samples" + ), + optparse::make_option( + c("-e", "--fusion_file_pp"), + type = "character", + default = NULL, + help = "file path to file that contains fusion information of primary-plus samples" + ), + optparse::make_option( + c("-s", "--metadata_file"), + type = "character", + default = NULL, + help = "file path to the histologies file" + ), + optparse::make_option( + c("-l", "--goi_list"), + type = "character", + default = NULL, + help = "comma-separated list of genes of interest files that contain the + genes to include on oncoprint" + ), + optparse::make_option( + c("-b", "--broad_histology_list"), + type = "character", + default = NULL, + help = "comma-separated list of `broad_histology` value to output numbers entering oncoprint" + ), + optparse::make_option( + c("-o", "--short_name_list"), + type = "character", + default = NULL, + help = "comma-separated list of file prefix for output tables" + ), + optparse::make_option( + c("--include_introns"), + action = "store_true", + default = FALSE, + help = "logical statement on whether to include intronic variants in oncoprint plot" + ) +) + +# Read the arguments passed +opt_parser <- optparse::OptionParser(option_list = option_list) +opt <- optparse::parse_args(opt_parser) + +# Define cnv_file, fusion_file, and genes object here as they still need to +# be defined for the `prepare_and_plot_oncoprint` custom function (the +# cnv_file specifically for the `read.maf` function within the custom function), +# even if they are NULL +broad_histology_list<-unlist(strsplit(opt$broad_histology_list,",")) +short_name_list<-unlist(strsplit(opt$short_name_list,",")) + +# Source the custom functions script +source( + file.path( + root_dir, + "analyses", + "oncoprint-landscape", + "util", + "oncoplot-functions.R" + ) +) + +#### Read in data -------------------------------------------------------------- + +# Read in metadata +metadata <- readr::read_tsv(opt$metadata_file, guess_max = 10000) %>% + dplyr::rename(Tumor_Sample_Barcode = sample_id) + +# Read in MAF file +maf_df_po <- data.table::fread(opt$maf_file_po, + stringsAsFactors = FALSE, + data.table = FALSE) +maf_df_pp <- data.table::fread(opt$maf_file_pp, + stringsAsFactors = FALSE, + data.table = FALSE) + +if (!opt$include_introns) { + maf_df_po <- maf_df_po %>% + dplyr::filter(Variant_Classification != "Intron") + + maf_df_pp <- maf_df_pp %>% + dplyr::filter(Variant_Classification != "Intron") +} + +# Read in cnv file +cnv_df_po <- readr::read_tsv(opt$cnv_file_po) +cnv_df_pp <- readr::read_tsv(opt$cnv_file_pp) + + +# Read in fusion file and join +fusion_df_po <- readr::read_tsv(opt$fusion_file_po) +fusion_df_pp <- readr::read_tsv(opt$fusion_file_pp) + + +#### Set up oncoprint annotation objects -------------------------------------- +oncoprint_n_table_po <- data.frame(matrix(ncol = 3, nrow = 0)) +oncoprint_n_table_pp <- data.frame(matrix(ncol = 3, nrow = 0)) + +colnames(oncoprint_n_table_po) <- c("broad_histology", "n_sample", "tumor_type") +colnames(oncoprint_n_table_pp) <- c("broad_histology", "n_sample", "tumor_type") + +for(i in 1:length(broad_histology_list)){ + histology_of_interest <- broad_histology_list[i] + + if (!histology_of_interest == "Other CNS") { + metadata_each <- metadata %>% + dplyr::filter(broad_histology == histology_of_interest) + } else { + metadata_each <- metadata %>% + dplyr::filter( + broad_histology %in% c( + "Ependymal tumor", + "Tumors of sellar region", + "Neuronal and mixed neuronal-glial tumor", + "Tumor of cranial and paraspinal nerves", + "Meningioma", + "Mesenchymal non-meningothelial tumor", + "Germ cell tumor", + "Choroid plexus tumor", + "Histiocytic tumor", + "Tumor of pineal region", + "Metastatic tumors", + "Other astrocytic tumor", + "Lymphoma", + "Melanocytic tumor", + "Other tumor" + ) + ) + } + # Now filter the remaining data files + maf_po_each <- maf_df_po %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + cnv_po_each <- cnv_df_po %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + fusion_po_each <- fusion_df_po %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + # get bs ids in each dataframe + maf_po_bsid <- maf_po_each %>% pull(Tumor_Sample_Barcode) %>% unique() + cnv_po_bsid <- cnv_po_each %>% pull(Tumor_Sample_Barcode) %>% unique() + fusion_po_bsid <- fusion_po_each %>% pull(Tumor_Sample_Barcode) %>% unique() + # take union + all_po_bsid <- union(maf_po_bsid, cnv_po_bsid) %>% union(fusion_po_bsid) + # write out broad histology and number of samples to a table + oncoprint_n_table_po[i,1] <- histology_of_interest + oncoprint_n_table_po[i,2] <- length(all_po_bsid) + oncoprint_n_table_po[i,3] <- "primary_only" + + # Now do the same thing for primary plus samples + maf_pp_each <- maf_df_pp %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + cnv_pp_each <- cnv_df_pp %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + fusion_pp_each <- fusion_df_pp %>% + dplyr::filter(Tumor_Sample_Barcode %in% metadata_each$Tumor_Sample_Barcode) + + # get bs ids in each dataframe + maf_pp_bsid <- maf_pp_each %>% pull(Tumor_Sample_Barcode) %>% unique() + cnv_pp_bsid <- cnv_pp_each %>% pull(Tumor_Sample_Barcode) %>% unique() + fusion_pp_bsid <- fusion_pp_each %>% pull(Tumor_Sample_Barcode) %>% unique() + # take union + all_pp_bsid <- union(maf_pp_bsid, cnv_pp_bsid) %>% union(fusion_pp_bsid) + # write out broad histology and number of samples to a table + oncoprint_n_table_pp[i,1] <- histology_of_interest + oncoprint_n_table_pp[i,2] <- length(all_pp_bsid) + oncoprint_n_table_pp[i,3] <- "primary-plus" + +} + +# write out n number entering oncoprint +bind_rows(oncoprint_n_table_pp, oncoprint_n_table_po) %>% + readr::write_tsv(file.path(results_dir, "sample_n_in_oncoprint.tsv")) + diff --git a/analyses/oncoprint-landscape/README.md b/analyses/oncoprint-landscape/README.md index e0df5754fa..613c0ab778 100644 --- a/analyses/oncoprint-landscape/README.md +++ b/analyses/oncoprint-landscape/README.md @@ -22,7 +22,8 @@ bash run-oncoprint.sh * Filtering via an [independent specimen file](https://alexslemonade.github.io/OpenPBTA-manuscript/#selection-of-independent-samples) is optional, but highly recommended. * `02-plot-oncoprint.R` takes the files from above and optionally a file or set of files (to be concatenated) that will restrict the set of genes that are being plotted in an OncoPrint. * Running this via `run-oncoprint.sh` will restrict plotting to a list of top mutated genes (generated in `analyses/interaction-plots/scripts/01-disease-specimen-lists.R`) and top genes with recurrent CNVs (generated in `analyses/focal-cn-file-preparation/06-find-recurrent-calls.Rmd`) - + * This script also returns tables summary of the total of number of samples that have alterations in gene of interest +* `03-oncoprint-n-count-table.R` counts the number of samples that enter oncoprint plotting (with or without alterations in genes of interest) for each broad histology group ### Folder Structure @@ -30,6 +31,7 @@ bash run-oncoprint.sh ├── 00-prepare-goi-lists.R ├── 01-map-to-sample_id.R ├── 02-plot-oncoprint.R +├── 03-oncoprint-n-count-table.R ├── README.md ├── data │   ├── embryonal-tumor_goi_list.tsv @@ -45,6 +47,10 @@ bash run-oncoprint.sh │   ├── primary-plus_*histology*_oncoprint.png │   ├── primary_only_*histology*_goi_oncoprint.png │   └── primary_only_*histology*_oncoprint.png +├── tables +│   ├── summary_n_in_oncoprint.tsv +│   ├── primary-plus_*histology*_summary_n.tsv +│   └── primary_only_*histology*_summary_n.tsv ├── run-oncoprint.sh └── util └── oncoplot-functions.R diff --git a/analyses/oncoprint-landscape/run-oncoprint.sh b/analyses/oncoprint-landscape/run-oncoprint.sh index aa428f58fb..0dea397684 100644 --- a/analyses/oncoprint-landscape/run-oncoprint.sh +++ b/analyses/oncoprint-landscape/run-oncoprint.sh @@ -74,7 +74,7 @@ declare -A labels=( ) declare -A goi_files=( - [lgat]="lgat_goi_list.tsv" + [lgat]="lgat_goi_list.tsv" [embryonal]="embryonal-tumor_goi_list.tsv" [hgat]="hgat_goi_list.tsv" [other]="other_goi_list.tsv" @@ -94,8 +94,8 @@ for histology in "${histologies[@]}"; do --fusion_file "${intermediate_directory}/${filename}_fusions.tsv" \ --metadata_file "${histologies_file}" \ --png_name "${filename}_${histology}_oncoprint.png" \ - --broad_histology "${labels[$histology]}" - + --broad_histology "${labels[$histology]}" + # Genes of interest only version of oncoprint Rscript --vanilla 02-plot-oncoprint.R \ --maf_file "${intermediate_directory}/${filename}_maf.tsv" \ @@ -105,7 +105,19 @@ for histology in "${histologies[@]}"; do --goi_list "${oncoprint_data_directory}/${goi_files[$histology]}" \ --top_n 20 \ --png_name "${filename}_${histology}_goi_oncoprint.png" \ - --broad_histology "${labels[$histology]}" + --broad_histology "${labels[$histology]}" \ + --output_table "${filename}_${histology}_oncoprint_summary_n.tsv" - done + done done + +Rscript --vanilla 03-oncoprint-n-count-table.R \ + --maf_file_po "${intermediate_directory}/primary_only_maf.tsv" \ + --cnv_file_po "${intermediate_directory}/primary_only_cnv.tsv" \ + --fusion_file_po "${intermediate_directory}/primary_only_fusions.tsv" \ + --maf_file_pp "${intermediate_directory}/primary-plus_maf.tsv" \ + --cnv_file_pp "${intermediate_directory}/primary-plus_cnv.tsv" \ + --fusion_file_pp "${intermediate_directory}/primary-plus_fusions.tsv" \ + --metadata_file "${histologies_file}" \ + --broad_histology_list "Low-grade astrocytic tumor,Embryonal tumor,Diffuse astrocytic and oligodendroglial tumor,Other CNS" \ + --short_name_list "lgat,embryonal,hgat,other" diff --git a/analyses/oncoprint-landscape/tables/primary-plus_embryonal_oncoprint_summary_n.tsv b/analyses/oncoprint-landscape/tables/primary-plus_embryonal_oncoprint_summary_n.tsv new file mode 100644 index 0000000000..81107ab5c5 --- /dev/null +++ b/analyses/oncoprint-landscape/tables/primary-plus_embryonal_oncoprint_summary_n.tsv @@ -0,0 +1,48 @@ +Hugo_Symbol 3'Flank 5'Flank Frame_Shift_Del Frame_Shift_Ins Fusion In_Frame_Ins Missense_Mutation Multi_Hit_Fusion Nonsense_Mutation Splice_Site 3'UTR Splice_Region Silent RNA 5'UTR total Amp Del CNV_total MutatedSamples AlteredSamples +CTNNB1 0 0 0 0 1 0 12 0 0 0 0 0 0 0 0 13 0 0 0 13 13 +DDX3X 1 0 0 0 0 1 7 0 1 1 1 0 0 0 1 13 0 0 0 12 12 +TP53 0 0 1 0 0 0 6 0 1 2 1 0 0 0 0 11 0 0 0 9 9 +KMT2C 0 0 2 2 0 0 2 0 1 0 2 0 1 0 0 10 0 0 0 9 9 +KDM6A 1 0 0 1 0 0 0 0 2 3 1 1 0 0 0 9 0 0 0 9 9 +KMT2D 0 0 2 2 0 0 1 0 3 1 0 0 0 0 0 9 0 0 0 8 8 +SMARCA4 0 1 0 0 0 0 7 0 0 0 0 0 0 0 0 8 0 0 0 6 6 +PTCH1 0 1 3 1 0 0 0 0 0 1 1 0 0 0 0 7 0 0 0 6 6 +TERT 0 4 0 0 0 0 0 0 0 0 0 1 0 0 0 5 1 0 1 4 5 +KSR2 0 1 0 0 0 0 0 0 0 0 3 0 0 0 0 4 0 0 0 4 4 +ATM 0 0 0 0 0 0 2 0 0 0 0 1 0 0 0 3 0 0 0 3 3 +CDK6 0 1 0 0 0 0 0 0 0 0 2 0 0 0 0 3 0 0 0 3 3 +IGFN1 1 0 0 0 0 0 1 0 0 0 0 0 1 0 0 3 0 0 0 3 3 +TCF4 1 1 0 0 0 0 1 0 0 0 0 0 0 0 0 3 0 0 0 3 3 +TTYH1 0 0 0 0 2 0 0 1 0 0 0 0 0 0 0 3 3 0 3 3 3 +ZIC1 0 0 0 0 0 0 3 0 0 0 0 0 0 0 0 3 0 0 0 3 3 +ZMYM3 1 0 0 0 0 0 0 0 1 0 0 0 1 0 0 3 0 0 0 3 3 +APC 0 0 0 0 0 0 0 0 1 0 1 0 0 0 0 2 0 0 0 2 2 +CREBBP 1 0 0 0 0 0 0 0 1 0 0 0 0 0 0 2 0 0 0 2 2 +CTDNEP1 0 0 0 1 0 0 0 0 1 0 0 0 0 0 0 2 0 0 0 2 2 +FOXO3 0 0 0 0 0 0 0 1 1 0 0 0 0 0 0 2 0 0 0 2 2 +GSE1 0 0 0 1 1 0 0 0 0 0 0 0 0 0 0 2 0 0 0 2 2 +KBTBD4 0 0 0 0 0 2 0 0 0 0 0 0 0 0 0 2 0 0 0 2 2 +MIR17HG 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 2 0 0 0 2 2 +PRKAR1A 0 1 0 0 0 0 0 0 0 0 1 0 0 0 0 2 1 0 1 2 3 +PTEN 0 0 0 0 0 0 0 0 0 2 0 0 0 0 0 2 0 0 0 1 1 +ARID1A 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +BCOR 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +CENPE 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +DICER1 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +DYNC2H1 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +FOXR2 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +MED12 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 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b/analyses/oncoprint-landscape/tables/primary-plus_hgat_oncoprint_summary_n.tsv @@ -0,0 +1,84 @@ +Hugo_Symbol 3'Flank 5'Flank Frame_Shift_Del Frame_Shift_Ins Fusion In_Frame_Del In_Frame_Ins Missense_Mutation Multi_Hit_Fusion Nonsense_Mutation Splice_Site 3'UTR Silent Splice_Region 5'UTR RNA total Amp Del CNV_total MutatedSamples AlteredSamples +TP53 6 0 2 0 0 1 0 42 0 7 2 1 2 1 0 0 64 0 0 0 44 44 +H3F3A 0 1 0 0 0 0 0 40 0 0 0 0 0 0 0 0 41 0 0 0 41 41 +ATRX 0 1 7 2 2 0 0 14 0 3 2 2 1 0 0 0 34 0 2 2 23 24 +NF1 1 2 8 2 1 0 0 4 0 8 2 2 1 0 0 0 31 0 0 0 17 17 +PIK3CA 0 1 0 0 0 4 0 9 0 0 0 4 0 0 0 0 18 0 0 0 14 14 +EGFR 1 0 0 0 1 0 1 14 0 0 0 5 2 0 1 0 25 1 0 1 12 13 +TERT 0 7 0 0 1 0 0 4 0 0 0 1 0 0 0 0 13 0 0 0 12 12 +MET 2 0 0 0 3 0 0 2 3 1 0 1 1 0 0 0 13 2 0 2 11 12 +PPM1D 1 0 2 2 0 0 0 1 0 5 0 1 0 0 0 0 12 1 0 1 11 12 +PTPN11 2 4 0 0 0 0 0 10 0 0 1 0 1 0 0 0 18 0 0 0 10 10 +PTEN 1 0 1 1 1 1 0 4 0 0 2 5 0 0 0 0 16 0 1 1 10 10 +NTRK3 5 2 0 0 3 0 0 2 0 0 0 9 0 0 0 0 21 0 0 0 9 9 +BCOR 0 2 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0 1 0 0 0 0 0 0 0 0 0 0 0 0 2 0 0 0 2 2 +YES1 1 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 0 0 2 2 +CDKN2B 1 3 0 0 0 0 0 0 0 0 0 0 0 0 0 0 4 0 1 1 1 2 +FGFR2 0 0 0 0 0 0 0 1 0 0 1 1 0 0 0 0 3 0 0 0 1 1 +APOBEC3H 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +CDK4 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 1 0 1 1 2 +HIST2H3C 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +ID2 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +ID3 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 1 0 0 0 1 1 +RB1 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 diff --git a/analyses/oncoprint-landscape/tables/primary_only_lgat_oncoprint_summary_n.tsv b/analyses/oncoprint-landscape/tables/primary_only_lgat_oncoprint_summary_n.tsv new file mode 100644 index 0000000000..b491babab8 --- /dev/null +++ b/analyses/oncoprint-landscape/tables/primary_only_lgat_oncoprint_summary_n.tsv @@ -0,0 +1,23 @@ +Hugo_Symbol 3'Flank 5'Flank Frame_Shift_Del Frame_Shift_Ins Fusion In_Frame_Del In_Frame_Ins Missense_Mutation Multi_Hit_Fusion Nonsense_Mutation Splice_Site 3'UTR Silent total MutatedSamples AlteredSamples +BRAF 3 0 1 1 99 0 4 36 2 0 0 2 1 149 140 140 +KIAA1549 0 0 0 0 98 0 0 0 0 0 0 0 0 98 98 98 +FGFR1 0 0 0 0 0 0 0 8 0 0 0 0 0 8 5 5 +NTRK2 0 1 0 0 4 0 0 0 0 0 0 0 0 5 5 5 +PIK3CA 0 0 0 0 0 0 0 5 0 0 0 0 0 5 5 5 +QKI 0 0 0 0 1 0 0 0 2 0 0 2 0 5 5 5 +KRAS 0 0 0 0 0 0 0 4 0 0 0 0 3 7 4 4 +RAF1 0 0 0 0 3 0 0 0 1 0 0 0 0 4 4 4 +MYB 0 0 0 0 2 0 0 0 1 0 0 0 0 3 3 3 +ROS1 0 0 0 0 3 0 0 0 0 0 0 0 0 3 3 3 +TP53 0 0 1 0 0 0 0 1 0 0 1 0 0 3 3 3 +ATRX 0 0 0 1 0 0 0 0 0 1 0 0 0 2 2 2 +FGFR2 0 0 0 0 2 0 0 0 0 0 0 0 0 2 2 2 +ALK 0 0 0 0 1 0 0 0 0 0 0 0 0 1 1 1 +CDKN2A 0 1 0 0 0 0 0 0 0 0 0 0 0 1 1 1 +H3F3A 0 1 0 0 0 0 0 0 0 0 0 0 0 1 1 1 +MAP2K1 0 0 0 0 0 1 0 0 0 0 0 0 0 1 1 1 +NTRK3 1 0 0 0 0 0 0 0 0 0 0 0 0 1 1 1 +PRKCA 0 0 0 0 1 0 0 0 0 0 0 0 0 1 1 1 +PTPN11 0 0 0 0 0 0 0 1 0 0 0 0 0 1 1 1 +TACC1 0 0 0 0 0 0 0 1 0 0 0 0 0 1 1 1 +TSC1 0 0 0 0 1 0 0 0 0 0 0 0 0 1 1 1 diff --git a/analyses/oncoprint-landscape/data/primary_only_n_per_cancer_group.tsv b/analyses/oncoprint-landscape/tables/primary_only_n_per_cancer_group.tsv similarity index 100% rename from analyses/oncoprint-landscape/data/primary_only_n_per_cancer_group.tsv rename to analyses/oncoprint-landscape/tables/primary_only_n_per_cancer_group.tsv diff --git a/analyses/oncoprint-landscape/tables/primary_only_other_oncoprint_summary_n.tsv b/analyses/oncoprint-landscape/tables/primary_only_other_oncoprint_summary_n.tsv new file mode 100644 index 0000000000..f5464618c1 --- /dev/null +++ b/analyses/oncoprint-landscape/tables/primary_only_other_oncoprint_summary_n.tsv @@ -0,0 +1,40 @@ +Hugo_Symbol 3'Flank 5'Flank Frame_Shift_Del Frame_Shift_Ins Fusion Missense_Mutation Multi_Hit_Fusion Nonsense_Mutation Splice_Site 3'UTR 5'UTR Silent total Amp Del CNV_total MutatedSamples AlteredSamples +CTNNB1 0 1 0 0 0 22 0 0 0 0 0 0 23 0 0 0 23 23 +C11orf95 0 1 0 0 14 0 1 0 0 0 0 0 16 0 0 0 16 16 +RELA 0 0 0 0 14 0 1 0 0 0 0 0 15 0 0 0 15 15 +NF2 0 0 6 1 2 1 0 4 2 0 0 0 16 0 0 0 14 14 +BRAF 1 0 0 0 3 2 1 0 0 0 0 0 7 0 0 0 7 7 +FGFR1 0 0 0 0 3 5 0 0 0 0 0 0 8 0 0 0 6 6 +TACC1 1 1 0 0 3 0 0 0 0 1 1 0 7 0 0 0 6 6 +EWSR1 0 1 0 0 5 0 0 0 0 0 0 0 6 0 0 0 6 6 +KRAS 0 1 0 0 1 3 0 0 0 0 0 0 5 0 0 0 5 5 +ERBB4 0 0 0 0 4 0 0 0 0 0 0 0 4 0 0 0 4 4 +TP53 1 0 0 0 1 0 0 0 3 0 0 0 5 0 0 0 3 3 +QKI 0 0 0 0 1 0 0 0 2 0 0 0 3 0 0 0 3 3 +SETD2 0 0 0 1 1 0 0 0 0 1 0 0 3 0 0 0 3 3 +YAP1 0 0 0 0 3 0 0 0 0 0 0 0 3 0 0 0 3 3 +PDGFRA 0 0 0 0 0 2 0 2 0 0 0 0 4 0 0 0 2 2 +IDH2 0 1 0 0 0 1 0 0 0 0 0 0 2 0 0 0 2 2 +MAML2 0 0 0 0 1 0 1 0 0 0 0 0 2 0 0 0 2 2 +MYB 1 0 0 0 1 0 0 0 0 0 0 0 2 0 0 0 2 2 +TERT 0 1 0 0 0 0 0 0 0 0 0 1 2 0 0 0 2 2 +AKT1 0 0 0 0 0 1 0 0 0 0 0 0 1 0 0 0 1 1 +AKT3 0 0 0 0 0 1 0 0 0 0 0 0 1 0 0 0 1 1 +ARHGAP26 0 0 0 0 1 0 0 0 0 0 0 0 1 0 0 0 1 1 +ARID1A 0 0 1 0 0 0 0 0 0 0 0 0 1 0 1 1 1 2 +ARL4D 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +CDC27 1 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +CDKN2A 1 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +CLDN1 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +EGFR 1 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +FAM118B 0 0 0 0 1 0 0 0 0 0 0 0 1 0 0 0 1 1 +FGFR3 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +IDH1 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 1 1 +L1CAM 0 0 0 0 0 0 0 0 0 0 0 1 1 0 0 0 1 1 +MAMLD1 0 0 0 0 0 0 0 0 0 0 0 1 1 0 0 0 1 1 +PBRM1 0 0 0 0 1 0 0 0 0 0 0 0 1 0 0 0 1 1 +PIK3CA 0 0 0 0 0 1 0 0 0 0 0 0 1 0 0 0 1 1 +PTEN 0 0 0 0 0 0 0 0 0 1 0 0 1 0 0 0 1 1 +SMAD4 0 0 0 0 0 0 0 0 0 1 0 0 1 0 0 0 1 1 +MYBL1 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 1 0 1 +SMARCB1 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 1 0 1 diff --git a/analyses/oncoprint-landscape/tables/sample_n_in_oncoprint.tsv b/analyses/oncoprint-landscape/tables/sample_n_in_oncoprint.tsv new file mode 100644 index 0000000000..c32e8596ca --- /dev/null +++ b/analyses/oncoprint-landscape/tables/sample_n_in_oncoprint.tsv @@ -0,0 +1,9 @@ +broad_histology n_sample tumor_type +Low-grade astrocytic tumor 263 primary-plus +Embryonal tumor 136 primary-plus +Diffuse astrocytic and oligodendroglial tumor 85 primary-plus +Other CNS 247 primary-plus +Low-grade astrocytic tumor 227 primary_only +Embryonal tumor 128 primary_only +Diffuse astrocytic and oligodendroglial tumor 61 primary_only +Other CNS 195 primary_only