R/response_viewer.R

In hiddengenome/deepG: deepG

#' Change nucleotides to values
#' 
#' @param nucleotides nucleotides from the genomic sequence
#' @export
nucleotide2value <- function(nucleotides){
  require(plyr)
  nuc <- unlist(strsplit(nucleotides, "", fixed = TRUE))
  values <- mapvalues(nuc, c("A", "C", "G", "T"), c(0, 0.33, 0.66, 1))
  return(values)
}

# Shiny app --------------------------------------------------------------------

#' This is a Shiny web application for the visualization of hidden states of
#' LSTM models from the package deepG. It also comes with 
#' the possibility to use own trained models.
#' 
#' @param sample character input string of text
#' @param states if states = TRUE, then load states from states_path
#' @param model.path path to trained model
#' @param fasta.path path to fasta files
#' @param states.path path to the .h5 file with the calculated states
#' @param start_position start from the dygraph
#' @param end_position end from the dygraph
#' @param batch.size number of samples to evaluate at once
#' @param vocabulary used vocabulary
#' @param layer_depth depth of layer to evaluate
#' @param cell_number cell_number showed in the dygraph
#' @param step frequency of sampling steps
#' @param padding TRUE/FALSE generate states for the first maxlen nucleotides
#' @export
visualizePrediction <- function(sample = "",
                                states = FALSE,
                                model.path = "",
                                fasta.path = "",
                                states.path = "",
                                start_position = 0,
                                end_position = 800,
                                batch.size = 200,
                                vocabulary = c("l","a","g","c","t"),
                                layer_depth = 1,
                                cell_number = 1,
                                step = 1,
                                padding = TRUE){

library(shiny)
library(Biostrings)
library(readr)
library(quantmod)
library(h5)
library(keras)
library(deepG)
library(DT)
library(pairsD3)
library(ggplot2)
library(dygraphs)
library(ape)

# UI (User inferace) -----------------------------------------------------------
ui <- fluidPage(titlePanel("Response Viewer for deepG", windowTitle = 'GenomeNet'),
                
                # Inputs -------------------------------------------------------
                tags$p(tags$b("GenomeNet:"),
                    "For training deep neural LSTM networks for genomic modeling and visualising their hidden states,
                    please see our", tags$a("Wiki", href="https://github.com/hiddengenome/deepG/wiki"), "for help."),
                    
                selectInput(
                    "selectinput_cell",
                    "Cell number(s):",
                    selected = cell_number,
                    choices = 1:125 ,
                    multiple = TRUE, 
                    width = "45%"),

                # Output -------------------------------------------------------
                tabsetPanel(tabPanel(
                    "Cell Response:", 
                    dygraphOutput("dygraph"), 
                    dygraphOutput("dygraph2", height = 80))))
# SERVER -----------------------------------------------------------------------
server <- function(input, output, session) {

  # load maxlen from the model
  
  if(is.null(states.path)){
  model <- keras::load_model_hdf5(model.path) 
  maxlen <- model$input$shape[1] }

  # get the hidden states of the input sequence
  dataset <- reactive({
      if (states == TRUE){
        progress <- shiny::Progress$new()
        progress$set(message = "Load generated states ...", value = 1)
        states <- readRowsFromH5(h5_path = states.path, complete = TRUE)
        on.exit(progress$close())
        states}
      else{
       if (sample == ""){
        progress <- shiny::Progress$new()
        progress$set(message = "Preprocessing and computing states from Fasta file...", value = 1)
        writeStatesByFastaEntries(fasta.path = fasta.path, model.path = model.path, step = step, layer_depth = layer_depth,
                                  vocabulary = vocabulary, batch.size = batch.size, filename = "fasta_states", 
                                  padding = padding, h5_path = "data")
        states <- readRowsFromH5(h5_path = "data/Nr1fasta_states.h5", complete = TRUE)
        on.exit(progress$close())}
      else{
        progress <- shiny::Progress$new()
        progress$set(message = "Preprocessing and computing states ...", value = 1)
        states <- writeStatesToH5(model.path = model.path, sequence = sample, batch.size = batch.size, 
                                  layer_depth = layer_depth, h5_filename = "states", vocabulary = vocabulary, 
                                  step = step, returnStates = TRUE, padding = padding)
        on.exit(progress$close())}
      states}})
  
  # Plotting -------------------------------------------------------------------
  output$dygraph <- renderDygraph({
    cell_num <- as.numeric(input$selectinput_cell)
    states_df <- dataset()[, cell_num]
    cell_df <- data.frame(pos = 1:nrow(dataset()), states_df)
    
    dy <- dygraph(cell_df, group = "a", main = "" ) %>%
      dyLegend(show = "onmouseover", hideOnMouseOut = FALSE)  %>%
      dyOptions(stepPlot = TRUE) %>% dyRangeSelector(dateWindow = c(start_position, end_position))
    dy <- dyUnzoom(dy)})
  
  output$dygraph2 <- renderDygraph({
    cell_df <- data.frame(pos = 1:nrow(dataset()),
                          rep(0,nrow(dataset())))
      genome <- sample
      
      if(states == FALSE){
        if (sample == ""){
          genome <- Biostrings::readDNAStringSet(fasta.path)
          genome <- paste0(paste(genome, collapse = "p"))}}
        else{print("No data about sequence, shows only the calculated states")
          genome <- ""}
      
      ribbonData <- nucleotide2value(genome) # nucleotides into values [A = 0; C = 0.33; G = 0.66: T = 1]}
    
    dy <- dygraph(cell_df, group = "a") %>%
      dyRibbon(data = ribbonData, top = 1, bottom = 0, palette=c("yellow", "red", "green", "blue"))
      # [A = yellow; C = red; G = green: T = blue]
    dy    
  })}
# Run the application ----------------------------------------------------------
shinyApp(ui = ui, server = server)}