inst/shinyapp/modules/modules-pcawg-unicox.R

ui.modules_pcawg_unicox <- function(id) {
  ns <- NS(id)
  fluidPage(
    fluidRow(
      column(
        3,
        wellPanel(
          shinyWidgets::prettyRadioButtons(
            inputId = ns("profile"), label = "Select a genomic profile:",
            choiceValues = c(
              "mRNA", "miRNA_TMM", "miRNA_UQ",
              "promoter_raw", "promoter_relative", "promoter_outlier",
              "fusion", "APOBEC"
            ),
            choiceNames = c(
              "mRNA Expression", "miRNA Expression (TMM)",
              "miRNA Expression (UQ)",
              "Raw Promoter Activity",
              "Relative Promoter Activity",
              "Promoter Outlier",
              "Gene Fusion",
              "APOBEC mutagenesis"
            ),
            animation = "jelly"
          ),
          selectizeInput(
            inputId = ns("Pancan_search"),
            label = "Input a gene or formula (as signature)",
            choices = NULL,
            width = "100%",
            options = list(
              create = TRUE,
              maxOptions = 5,
              placeholder = "Enter a gene symbol, e.g. TP53",
              plugins = list("restore_on_backspace")
            )
          ),
          # selectInput(inputId = ns("measure"), label = "Select Measure for plot", choices = c("OS", "PFI", "DSS", "DFI"), selected = "OS"),
          selectInput(inputId = ns("threshold"), label = "Select Threshold for plot", choices = c(0.25, 0.5), selected = 0.5),
          colourpicker::colourInput(inputId = ns("first_col"), "First color", "#6A6F68"),
          colourpicker::colourInput(inputId = ns("second_col"), "Second color", "#E31A1C"),
          colourpicker::colourInput(inputId = ns("third_col"), "Third color", "#377DB8"),
          tags$hr(style = "border:none; border-top:2px solid #5E81AC;"),
          shinyWidgets::actionBttn(
            inputId = ns("search_bttn"),
            label = "Go!",
            style = "gradient",
            icon = icon("search"),
            color = "primary",
            block = TRUE,
            size = "sm"
          )),
          wellPanel(
            numericInput(inputId = ns("height"), label = "Height", value = 8),
            numericInput(inputId = ns("width"), label = "Width", value = 6),
            prettyRadioButtons(
              inputId = ns("device"),
              label = "Choose plot format",
              choices = c("pdf", "png"),
              selected = "pdf",
              inline = TRUE,
              icon = icon("check"),
              animation = "jelly",
              fill = TRUE
            ),
            downloadBttn(
              outputId = ns("download"),
              style = "gradient",
              color = "default",
              block = TRUE,
              size = "sm"
            )
          )
        ),
      column(
        9,
        plotOutput(ns("unicox_gene_tree"), height = "500px",width = "350px"),
        hr(),
        h5("NOTEs:"),
        p("1. We define gene in certain cancer type as risky (log(Hazard Ratio) > 0) or protective (log(Hazard Ratio) < 0) or NS (No statistical significance, P value > 0.05)"),
        p("2. We divide patients into different groups for comparison according to gene expression, you could choose the threshold for grouping (0.5 by default)"),
        p("3. ", tags$a(href = "https://xenabrowser.net/datapages/?cohort=PCAWG%20(specimen%20centric)&removeHub=https%3A%2F%2Fxena.treehouse.gi.ucsc.edu%3A443&removeHub=https%3A%2F%2Fatacseq.xenahubs.net", "Genomic profile data source")),
        DT::DTOutput(outputId = ns("tbl")),
        shinyjs::hidden(
          wellPanel(
            id = ns("save_csv"),
            downloadButton(ns("downloadTable"), "Save as csv")
          )
        )
      )
    )
  )
}


server.modules_pcawg_unicox <- function(input, output, session) {
  ns <- session$ns

  profile_choices <- reactive({
    switch(input$profile,
      mRNA = list(all = pancan_identifiers$gene, default = "TP53"),
      miRNA_TMM = list(all = pancan_identifiers$miRNA, default = "hsa-miR-769-3p"),
      miRNA_UQ = list(all = pancan_identifiers$miRNA, default = "hsa-miR-769-3p"),
      promoter_raw = list(all = names(load_data("pcawg_promoter_id")), default = "1:169863093:SCYL3"),
      promoter_relative = list(all = names(load_data("pcawg_promoter_id")), default = "1:169863093:SCYL3"),
      promoter_outlier = list(all = names(load_data("pcawg_promoter_id")), default = "1:169863093:SCYL3"),
      fusion = list(all = pancan_identifiers$gene, default = "DPM1"),
      APOBEC = list(all = c(
        "tCa_MutLoad_MinEstimate", "APOBECtCa_enrich",
        "A3A_or_A3B", "APOBEC_tCa_enrich_quartile", "APOBECrtCa_enrich",
        "APOBECytCa_enrich", "APOBECytCa_enrich-APOBECrtCa_enrich",
        "BH_Fisher_p-value_tCa", "ntca+tgan", "rtCa_to_G+rtCa_to_T",
        "rtca+tgay", "tCa_to_G+tCa_to_T",
        "ytCa_rtCa_BH_Fisher_p-value", "ytCa_rtCa_Fisher_p-value", "ytCa_to_G+ytCa_to_T",
        "ytca+tgar"
      ), default = "APOBECtCa_enrich"),
      list(all = "NONE", default = "NONE")
    )
  })

  observe({
    updateSelectizeInput(
      session,
      "Pancan_search",
      choices = profile_choices()$all,
      selected = profile_choices()$default,
      server = TRUE
    )
  })

  # Show waiter for plot
  w <- waiter::Waiter$new(id = ns("unicox_gene_tree"), html = waiter::spin_hexdots(), color = "white")

  colors <- reactive({
    c(input$first_col, input$second_col, input$third_col)
  })

  observeEvent(input$search_bttn, {
    if (nchar(input$Pancan_search) >= 1) {
      shinyjs::show(id = "save_csv")
    } else {
      shinyjs::hide(id = "save_csv")
    }
  })

  plot_func <- eventReactive(input$search_bttn, {
    if (nchar(input$Pancan_search) >= 1) {
      p <- vis_pcawg_unicox_tree(
        Gene = input$Pancan_search,
        # measure = input$measure,
        threshold = input$threshold,
        data_type = input$profile,
        values = colors()
      )
      pdata <- p$data %>%
        as.data.frame() %>%
        dplyr::select(cancer, measure, n_contrast, n_ref, beta, HR_log, lower_95_log, upper_95_log, Type, p.value)
      return(list(plot = p, data = pdata))
    }
  })

  output$unicox_gene_tree <- renderPlot({
    w$show() # Waiter add-ins
    plot_func()$plot
  })

  output$download <- downloadHandler(
    filename = function() {
      paste0(input$Pancan_search, "_", input$profile, "_", input$measure, "_pcawg_unicox.", input$device)
    },
    content = function(file) {
      p <- plot_func()$plot
      if (input$device == "pdf") {
        pdf(file, width = input$width, height = input$height)
        print(p)
        dev.off()
      } else {
        png(file, width = input$width, height = input$height, res = 600, units = "in")
        print(p)
        dev.off()
      }
    }
  )


  output$tbl <- renderDT(
    plot_func()$data,
    options = list(lengthChange = FALSE)
  )

  output$downloadTable <- downloadHandler(
    filename = function() {
      paste0(input$Pancan_search, "_", input$profile, "_", input$measure, "_pcawg_unicox.csv")
    },
    content = function(file) {
      write.csv(plot_func()$data, file, row.names = FALSE)
    }
  )
}

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UCSCXenaShiny documentation built on March 7, 2023, 7 p.m.