#' @title UI of the surface plot module
#'
#' @param id The namespace id.
#'
moduleSurfacePlotUI <- function(id){
ns <- shiny::NS(id)
shiny::tagList(
shiny::column(width = 12,
shiny::wellPanel(
shiny::fluidRow(
shiny::column(width = 4,
shiny::fluidRow(
shiny::column(width = 6, shiny::uiOutput(ns("sample_opts"))),
shiny::column(width = 6, shiny::uiOutput(ns("aes_clr_opts")))
),
shiny::fluidRow(
shiny::uiOutput(ns("aes_clr_opts_detailed")),
shiny::conditionalPanel(
condition = "input.aes_clr_opts == 'gene_sets'", ns = ns,
shinyWidgets::pickerInput(ns("method_gs"),
label = "Gene-set method:",
choices = c("Mean" = "mean",
"Gene Set Variation Analysis" = "gsva",
"Gene Set Enrichment Analysis" = "ssgsea",
"Z-Score" = "zscore",
"Plage" = "plage" )))
),
shiny::fluidRow(
shiny::column(width = 6, shiny::uiOutput(ns("pt_clrsp"))),
shiny::column(width = 6, shiny::uiOutput(ns("pt_clrp")))
),
shiny::fluidRow(
shiny::column(width = 6,
shiny::sliderInput(ns("pt_size"), label = "Size of points:", min = 1, max = 10, step = 0.05, value = 2.75),
shiny::sliderInput(ns("pt_alpha"), label = "Transparency of points:", min = 0.01, max = 0.99, step = 0.01, value = 0.15),
shiny::uiOutput(ns("pt_smooth"))
),
shiny::column(width = 6,
shiny::uiOutput(ns("scale_color_min")),
shiny::uiOutput(ns("scale_color_mid")),
shiny::uiOutput(ns("scale_color_max"))
)
),
shiny::HTML("<br>")
),
shiny::column(width = 8,
shiny::plotOutput(ns("surface_plot"), dblclick = ns("surface_plot_dblclick")),
shiny::HTML("<br>"),
shiny::fluidRow(
shiny::column(width = 4,
shiny::actionButton(ns("update_plot"), label = "Plot & Update")),
shiny::column(width = 8,
shinyWidgets::checkboxGroupButtons(inputId = ns("display_add_ons"),
label = NULL,
selected = "legend",
choices = c("Legend" = "legend",
"Image" = "image",
"Title" = "title",
"Coordinates" = "coords",
"Segmentation" = "segmentation"),
direction = "horizontal",
justified = FALSE,
individual = FALSE)
)
)
)
)
)
)
)
}
#' @title Server of the surface plot module
#'
#' @param id The namespace id.
#' @param object A valid spata-object.
#' @param final_plot The final plot that is to be displayed. (See details.).
#' @param reactive_object A valid (reactive) spata-object.
#'
#' @return A reactive list with several slots:
#' \enumerate{
#' \item $assembled_plot() The surface plot as a ggplot-object.
#' \item $dblclick() A list containing information regarding the double clicked position in the plot.
#' \item $current_setting() A list with information about the settings of \code{assembled_plot} (e.g. sample, color_to, smooth, smoothing_span ...)}
#'
#' @details The argument \code{final_plot} takes a ggplot object as input which is going to be displayed as the final plot. This allows to
#' adjust the output of \code{$assembled_plot()} outside of the module. If no further adjustment is needed determine \code{final_plot} as:
#' \code{shiny::reactive(*module_return_variable*()$assembled_plot())}
#'
moduleSurfacePlotServer <- function(id,
object,
final_plot,
reactive_object,
highlighted = shiny::reactive( FALSE )){
shiny::moduleServer(
id = id,
module = function(input,
output,
session){
# Reactive values -----------------------------------------------------------
return_plot <- shiny::reactiveVal(list())
current <- shiny::reactiveValues(
sample = samples(object)[1],
color_code = "gene_sets",
gene_set = base::character(1),
method_gs = base::character(1),
genes = base::character(1),
feature = base::character(1),
pt_size = base::numeric(1),
pt_clrp = base::character(1),
pt_clrsp = base::character(1),
smooth = base::logical(1),
span = base::numeric()
)
reset_select_gene_sets <- shiny::reactiveVal(value = 0)
reset_select_genes <- shiny::reactiveVal(value = 0)
all_features <- getFeatureNames(object) %>% base::unname()
all_gene_sets <- getGeneSets(object = object)
all_genes <- getGenes(object = object, in_sample = "all")
smooth_values <- base::seq(0.01, 0.25, by = 0.01) %>%
base::round(digits = 3) %>%
base::unique()
all_values <- c(0, smooth_values)
# -----
# Render UIs and Outputs --------------------------------------------------
# update transparency
shiny::observeEvent(eventExpr = highlighted(), {
if(base::isTRUE(highlighted())){
shiny::updateSliderInput(session,
inputId = "pt_alpha",
label = "Transparency of points",
min = 0.01,
max = 0.99,
step = 0.01,
value = 0.75)
} else if(base::isFALSE(highlighted())){
shiny::updateSliderInput(session,
inputId = "pt_alpha",
label = "Transparency of points",
min = 0.01,
max = 0.99,
step = 0.01,
value = 0.15)
}
})
# Main select input -------------------------------------------------------
output$sample_opts <- shiny::renderUI({
ns <- session$ns
shinyWidgets::pickerInput(ns("sample_opts"),
label = "Choose sample:",
choices = samples(object),
selected = samples(object)[1])
})
output$aes_clr_opts <- shiny::renderUI({
ns <- session$ns
shinyWidgets::pickerInput(ns("aes_clr_opts"),
label = "Choose colour code:",
choices = c("Gene set" = "gene_sets",
"Genes" = "genes",
"Feature" = "feature"),
selected = "features")
})
select_gene_sets <- shiny::eventReactive(reset_select_gene_sets(),{
ns <- session$ns
shinyWidgets::pickerInput(inputId = ns("aes_clr_opts_detailed"),
label = "Choose gene set:",
choices = all_gene_sets,
selected = all_gene_sets[1],
options = list(`live-search` = TRUE),
multiple = F)
})
select_genes <- shiny::eventReactive(reset_select_genes(),{
ns <- session$ns
shiny::tagList(
shinyWidgets::pickerInput(inputId = ns("aes_clr_opts_detailed"),
label = "Choose gene(s):",
choices = all_genes,
selected = all_genes[1],
options = shinyWidgets::pickerOptions(
liveSearch = TRUE,
actionsBox = TRUE),
multiple = TRUE),
shiny::checkboxInput(ns("reset_select_genes"),
label = "Automatic reset",
value = FALSE))
})
select_features <- shiny::reactive({
ns <- session$ns
shinyWidgets::pickerInput(inputId = ns("aes_clr_opts_detailed"),
label = "Choose feature:",
choices = all_features[all_features != "sample"],
options = shinyWidgets::pickerOptions(
liveSearch = TRUE,
actionsBox = TRUE),
multiple = F)
})
output$aes_clr_opts_detailed <- shiny::renderUI({
shiny::req(input$aes_clr_opts)
if(input$aes_clr_opts == "gene_sets"){
return(select_gene_sets())
} else if(input$aes_clr_opts == "genes"){
return(select_genes())
} else if(input$aes_clr_opts == "feature"){
return(select_features())
}
})
# -----
# Color select input ------------------------------------------------------
output$pt_clrsp <- shiny::renderUI({
ns <- session$ns
shinyWidgets::pickerInput(ns("pt_clrsp"),
label = "Color spectrum:",
choices = all_colorspectra(),
options = list(
`live-search` = TRUE
),
multiple = FALSE,
selected = "inferno")
})
output$pt_clrp <- shiny::renderUI({
ns <- session$ns
shinyWidgets::pickerInput(ns("pt_clrp"),
choices = c(
"MILO Research Group" = "milo",
"Journal of Oncology" = "jco",
"Nature Publishing Group" = "npg",
"American Association for the Advancement" = "aaas",
"New England Journal of Medicine" = "nejm",
"Lancet Oncology" = "lo",
"The Journal of the American Medical Association" = "jama",
"University of Chicago" = "uc"),
label = "Color panel:",
multiple = FALSE,
choicesOpt = list(
subtext = stringr::str_c("colors: ", c(20, base::rep(10,7))),
`dropdown-align-center` = TRUE
),
selected = "milo")
})
# -----
# Plot tweaking slider inputs ---------------------------------------------
output$scale_color_min <- shiny::renderUI({
shiny::validate(
shiny::need(base::is.numeric(color_variable()),
message = "Need numeric color-feature to scale minimum & maximum.",
label = "Color scale minimum")
)
ns <- session$ns
shiny::sliderInput(ns("scale_color_min"),
label = "Color scale minimum:",
min = color_min(),
max = color_max(),
value = color_min(),
step = 0.01)
})
output$scale_color_max <- shiny::renderUI({
shiny::validate(
shiny::need(expr = base::is.numeric(color_variable()),
message = "Need numeric color-feature to scale maxmimum.",
label = "Color scale maximum:")
)
ns <- session$ns
shiny::sliderInput(ns("scale_color_max"),
label = "Color scale maximum:",
min = color_min(),
max = color_max(),
value = color_max(),
step = 0.01)
})
output$scale_color_mid <- shiny::renderUI({
shiny::req(base::is.numeric(color_variable()))
ns <- session$ns
shiny::sliderInput(ns("scale_color_mid"),
label = "Color scale mid:",
min = color_min() * 1.1,
max = color_max() * 0.9,
value = color_median(),
step = 0.01)
})
output$pt_smooth <- shiny::renderUI({
ns <- session$ns
shinyWidgets::sliderTextInput(
inputId = ns("pt_smooth"),
label = "Spatial smoothing:",
choices = all_values,
grid = TRUE,
selected = 0
)
})
# -----
# Plot assembling ---------------------------------------------------------
output$surface_plot <- shiny::renderPlot({
shiny::req(final_plot())
final_plot()
})
# -----
# Plot add-ons ------------------------------------------------------------
#----- Image add-on -----#
image_add_on <- shiny::reactive({
## set up background
if("image" %in% input$display_add_ons){
## extract image info
img_info <-
image(object, of_sample = current$sample) %>%
grDevices::as.raster() %>%
magick::image_read() %>%
magick::image_info()
st_image <-
grDevices::as.raster(image(object, of_sample = current$sample)) %>%
magick::image_read() %>% magick::image_flip()
image_add_on <-
ggplot2::annotation_raster(raster = st_image,
xmin = 0, ymin = 0,
xmax = img_info$width,
ymax = img_info$height)
} else {
image_add_on <- NULL
}
})
#----- Geom point add-on -----#
# sample coordinates
sample_coords <- shiny::reactive({
sample_coords <-
getCoordinates(object = object, of_sample = current$sample)
return(sample_coords)
})
# rna_assay
rna_assay <- shiny::reactive({
rna_assay <-
exprMtr(object = object, of_sample = current$sample)
return(rna_assay)
})
# gene_vls
gene_vls <- shiny::reactive({
genes <- current$genes
# compute mean if neccessary
if(base::length(genes) > 1){
rna_assay <- base::colMeans(rna_assay()[genes,])
} else {
rna_assay <- rna_assay()[genes,]
}
# convert to data frame
gene_vls <-
rna_assay %>%
as.data.frame() %>%
magrittr::set_colnames(value = "expr_score") %>%
tibble::rownames_to_column(var = "barcodes")
return(gene_vls)
})
# geneset_vls
geneset_vls <- shiny::reactive({
shiny::req(current$gene_set)
gene_set_df <- object@used_genesets
genes <-
gene_set_df %>%
dplyr::filter(ont == current$gene_set) %>%
dplyr::filter(gene %in% base::rownames(rna_assay())) %>%
dplyr::pull(gene)
if(current$method_gs == "mean"){
geneset_vls <-
base::colMeans(rna_assay()[genes, ]) %>%
base::as.data.frame() %>%
magrittr::set_colnames(value = "expr_score") %>%
tibble::rownames_to_column(var = "barcodes")
} else if(current$method_gs %in% c("gsva", "ssgsea", "zscore", "plage")) {
shiny::showNotification(
ui = stringr::str_c("Calculating gene set score according to method: '", current$method_gs, "'. This might take a few moments.", sep = ""),
type = "message")
geneset_vls <-
GSVA::gsva(expr = rna_assay()[genes,], gset.idx.list = gene_set_df, mx.diff = 1, parallel.sz = 2, method = current$method_gs, verbose = F) %>%
base::t() %>%
base::as.data.frame() %>%
magrittr::set_colnames(value = "expr_score") %>%
tibble::rownames_to_column(var = "barcodes")
}
return(geneset_vls)
})
# fdata
fdata <- shiny::reactive({
fdata <-
featureData(object = object, of_sample = current$sample)[, c("barcodes", current$feature)]
return(fdata)
})
# joined data.frame
joined_df <- shiny::reactive({
if(current$color_code == "genes"){
joined_df <-
dplyr::left_join(x = sample_coords(), y = gene_vls(), by = "barcodes")
} else if(current$color_code == "gene_sets"){
joined_df <-
dplyr::left_join(x = sample_coords(), y = geneset_vls(), by = "barcodes")
} else if(current$color_code == "feature"){
joined_df <-
dplyr::left_join(x = sample_coords(), y = fdata(), by = c("barcodes"))
}
return(joined_df)
})
# variable
variable <- shiny::reactive({
if(current$color_code %in% c("genes", "gene_sets")){
variable <- "expr_score"
} else if(current$color_code == "feature") {
variable <- current$feature
}
return(variable)
})
# color variable
color_variable <- shiny::reactive({
dplyr::pull(smoothed_df(), variable())
})
color_min <- shiny::reactive({
base::min(color_variable()) %>%
base::round(digits = 2)
})
color_max <- shiny::reactive({
base::max(color_variable()) %>%
base::round(digits = 2)
})
color_median <- shiny::reactive({
stats::median(color_variable()) %>%
base::round(digits = 2)
})
# smoothed_df
smoothed_df <- shiny::reactive({
shiny::validate(
shiny::need(joined_df(), message = "Click on 'Plot & Update' to display the plot.")
)
if(base::as.numeric(input$pt_smooth) != 0){
smoothed_df <-
hlpr_smooth_shiny(coords_df = joined_df(),
variable = variable(),
smooth_span = base::as.numeric(input$pt_smooth))
if(current$color_code %in% c("genes", "gene_sets")){
smoothed_df <-
purrr::imap_dfr(.x = smoothed_df,
.f = hlpr_normalize_imap,
aspect = "",
subset = variable())
}
base::return(smoothed_df)
} else {
if(current$color_code %in% c("genes", "gene_sets")){
ret_imap_dfr <-
purrr::imap_dfr(.x = joined_df(),
.f = hlpr_normalize_imap,
aspect = "",
subset = variable())
base::return(ret_imap_dfr)
} else {
base::return(joined_df())
}
}
})
# geom_point_add_on
geom_point_add_on <- shiny::reactive({
#color <- dplyr::pull(.data = smoothed_df(), variable())
add_on <-
list(
ggplot2::geom_point(data = smoothed_df(),
mapping = ggplot2::aes(x = x, y = y, color = .data[[variable()]]),
size = input$pt_size,
alpha = (1-input$pt_alpha))
)
return(add_on)
})
#----- Scale color add-on -----#
color_add_on <- shiny::reactive({
color_min <- input$scale_color_min
color_max <- input$scale_color_max
color_mid <- input$scale_color_mid
if(base::is.numeric(color_variable())){
if(current$pt_clrsp %in% all_colorspectra()[["Diverging"]]){
add_on <-
confuns::scale_color_add_on(clrsp = current$pt_clrsp,
limits = c(color_min,
color_max),
mid = color_mid,
oob = scales::squish)
} else {
add_on <-
confuns::scale_color_add_on(clrsp = current$pt_clrsp,
limits = c(color_min,
color_max),
oob = scales::squish)
}
} else if(!base::is.numeric(color_variable())){
add_on <-
list(confuns::scale_color_add_on(variable = "discrete", clrp = current$pt_clrp),
ggplot2::guides(color = ggplot2::guide_legend(override.aes = list(size = 5))))
}
return(add_on)
})
#----- Theme add-ons -----#
coords_add_on <- shiny::reactive({
if("coords" %in% input$display_add_ons){
add_on <-
list(ggplot2::theme_bw(),
ggplot2::theme(
axis.ticks = ggplot2::element_blank(),
axis.title = ggplot2::element_blank()
))
} else {
add_on <-
list(ggplot2::theme_void())
}
return(add_on)
})
legend_add_on <- shiny::reactive({
if("legend" %in% input$display_add_ons){
if(current$color_code %in% c("gene_sets", "genes")){
legend_title = "Expr.\nscore"
} else {
legend_title = current$feature
}
add_on <-
list(ggplot2::labs(color = legend_title))
} else {
add_on <-
list(ggplot2::theme(legend.position = "none"))
}
return(add_on)
})
title_add_on <- shiny::reactive({
if("title" %in% input$display_add_ons){
if(current$color_code == "genes"){
genes <- current$genes
if(length(genes) > 5){
genes <- c(genes[1:5], stringr::str_c("... +", (length(genes)-5), sep = " "))
}
genes_string <- stringr::str_c(genes, collapse = ", ")
plot_title <- stringr::str_c("Genes:", genes_string, sep = " ")
} else if(current$color_code == "gene_sets"){
gene_set <- current$gene_set
gene_set_string <- stringr::str_c(gene_set, " (", current$method_gs, ")", sep = "")
plot_title <- stringr::str_c("Gene set:", gene_set_string, sep = " ")
} else {
plot_title <- stringr::str_c("Feature:", current$feature, sep = " ")
}
add_on <- ggplot2::labs(title = plot_title)
} else {
add_on <- NULL
}
return(add_on)
})
segmentation_add_on <- reactive({
if("segmentation" %in% input$display_add_ons){
if(nrow(segmentation_df()) == 0){
showNotification(ui = stringr::str_c("Sample", current$sample, "has not been segmented so far.", sep = " "))
return(list())
} else {
segm_layer <-
list(
ggalt::geom_encircle(data = segmentation_df(), alpha = 0.75, expand = 0.025,
mapping = ggplot2::aes(x = x, y = y, group = segment, fill = segment)),
confuns::scale_color_add_on(aes = "fill", variable = "discrete", clrp = "milo", guide = FALSE)
)
base::return(segm_layer)
}
} else {
base::return(list())
}
})
segmentation_df <- reactive({
segm_df <- joinWith(object = reactive_object(),
spata_df = getCoordinates(reactive_object(), current$sample),
features = "segment",
verbose = FALSE) %>%
dplyr::filter(segment != "")
return(segm_df)
})
# -----
# Assembled plot ----------------------------------------------------------
assembled_plot <- shiny::reactive({
shiny::req(input$update_plot)
ggplot2::ggplot() +
image_add_on() +
geom_point_add_on() +
color_add_on() +
legend_add_on() +
title_add_on() +
segmentation_add_on() +
ggplot2::coord_equal() +
coords_add_on()
})
# -----
# Observe events ----------------------------------------------------------
# update plot by updating reactive values
oe <- shiny::observeEvent(input$update_plot, {
current$sample = input$sample_opts
current$color_code = input$aes_clr_opts
if(current$color_code == "genes"){
current$genes = input$aes_clr_opts_detailed
} else if(current$color_code == "gene_sets"){
current$gene_set = input$aes_clr_opts_detailed
current$method_gs = input$method_gs
} else if(current$color_code == "feature"){
current$feature = input$aes_clr_opts_detailed
}
current$pt_size = input$pt_size
current$pt_clrsp = input$pt_clrsp
current$pt_clrp = input$pt_clrp
current$pt_alpha = input$pt_alpha
if(base::isTRUE(input$reset_select_genes) &&
current$color_code == "genes"){
reset_select_genes((reset_select_genes() + 1))
}
})
# -----
# Return values -----------------------------------------------------------
return_list <- shiny::reactive({
list(
assembled_plot = shiny::reactive({assembled_plot()}),
dblclick = shiny::reactive({input$surface_plot_dblclick}),
current_setting = shiny::reactive({current}),
smoothed_df = shiny::reactive({smoothed_df()}),
variable = shiny::reactive({variable()}),
variable_name = shiny::reactive(input$aes_clr_opts_detailed),
pt_size_reactive = shiny::reactive(input$pt_size)
)
})
base::return(return_list)
# -----
})
}
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