-
-
Notifications
You must be signed in to change notification settings - Fork 2
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
UI elements do not refresh when filter removed #288
Comments
I think this is a bigger issue, not necesserilly just in modules from Encodings do not get refreshed when filters are edited in the filter panel. I will open an issue in |
This happens for all plots for their all UI elements. I will change the name of the issue. teal.goshawk/R/tm_g_gh_boxplot.R Lines 330 to 345 in 28735c8
Other plots have similar code, so once we figure this out for a boxplot, we can figure this out for the rest of the plots in here. |
I was able to create a minimal reproducible example with an open data. I believe the main reason of this behavior is the To reproduce the issue:
Simple Applibrary(teal)
library(teal.modules.general)
library(teal.goshawk)
data <- teal_data()
data <- within(data, {
library(dplyr)
library(nestcolor)
library(stringr)
# use non-exported function from goshawk
h_identify_loq_values <- getFromNamespace("h_identify_loq_values", "goshawk")
# original ARM value = dose value
arm_mapping <- list(
"A: Drug X" = "150mg QD",
"B: Placebo" = "Placebo",
"C: Combination" = "Combination"
)
set.seed(1)
ADSL <- rADSL
ADLB <- rADLB
var_labels <- lapply(ADLB, function(x) attributes(x)$label)
ADLB <- ADLB %>%
mutate(
AVISITCD = case_when(
AVISIT == "SCREENING" ~ "SCR",
AVISIT == "BASELINE" ~ "BL",
grepl("WEEK", AVISIT) ~ paste("W", str_extract(AVISIT, "(?<=(WEEK ))[0-9]+")),
TRUE ~ as.character(NA)
),
AVISITCDN = case_when(
AVISITCD == "SCR" ~ -2,
AVISITCD == "BL" ~ 0,
grepl("W", AVISITCD) ~ as.numeric(gsub("[^0-9]*", "", AVISITCD)),
TRUE ~ as.numeric(NA)
),
AVISITCD = factor(AVISITCD) %>% reorder(AVISITCDN),
TRTORD = case_when(
ARMCD == "ARM C" ~ 1,
ARMCD == "ARM B" ~ 2,
ARMCD == "ARM A" ~ 3
),
ARM = as.character(arm_mapping[match(ARM, names(arm_mapping))]),
ARM = factor(ARM) %>% reorder(TRTORD),
ACTARM = as.character(arm_mapping[match(ACTARM, names(arm_mapping))]),
ACTARM = factor(ACTARM) %>% reorder(TRTORD),
ANRLO = 50,
ANRHI = 75
) %>%
rowwise() %>%
group_by(PARAMCD) %>%
mutate(LBSTRESC = ifelse(
USUBJID %in% sample(USUBJID, 1, replace = TRUE),
paste("<", round(runif(1, min = 25, max = 30))), LBSTRESC
)) %>%
mutate(LBSTRESC = ifelse(
USUBJID %in% sample(USUBJID, 1, replace = TRUE),
paste(">", round(runif(1, min = 70, max = 75))), LBSTRESC
)) %>%
ungroup()
attr(ADLB[["ARM"]], "label") <- var_labels[["ARM"]]
attr(ADLB[["ACTARM"]], "label") <- var_labels[["ACTARM"]]
attr(ADLB[["ANRLO"]], "label") <- "Analysis Normal Range Lower Limit"
attr(ADLB[["ANRHI"]], "label") <- "Analysis Normal Range Upper Limit"
# add LLOQ and ULOQ variables
ALB_LOQS <- h_identify_loq_values(ADLB, "LOQFL")
ADLB <- left_join(ADLB, ALB_LOQS, by = "PARAM")
})
datanames <- c("ADSL", "ADLB")
datanames(data) <- datanames
join_keys(data) <- default_cdisc_join_keys[datanames]
app <- init(
data = data,
modules = modules(
tm_data_table(label = "View Data"),
tm_g_gh_boxplot(
label = "Box Plot",
dataname = "ADLB",
param_var = "PARAMCD",
param = choices_selected(choices = value_choices("ADLB", "PARAMCD", "PARAM")),
yaxis_var = choices_selected(c("AVAL", "BASE", "CHG"), "AVAL"),
xaxis_var = choices_selected(c("ACTARM", "ARM", "AVISITCD", "STUDYID"), "ARM"),
facet_var = choices_selected(c("ACTARM", "ARM", "AVISITCD", "SEX"), "AVISITCD"),
trt_group = choices_selected(c("ARM", "ACTARM"), "ARM"),
loq_legend = TRUE,
rotate_xlab = FALSE,
hline_arb = c(60, 55),
hline_arb_color = c("grey", "red"),
hline_arb_label = c("default_hori_A", "default_hori_B"),
hline_vars = c("ANRHI", "ANRLO", "ULOQN", "LLOQN"),
hline_vars_colors = c("pink", "brown", "purple", "black"),
)
)
)
if (interactive()) {
shinyApp(app$ui, app$server)
}
|
@npaszty @gogonzo we are currently running a huge overhaul in |
thanks for looking into this. sounds like a big deal. this issue can be replicated in the teal.gallery app so that's a working example. what I noticed in the teal.gallery app is that all the modules fail to produce a plot because the "Select a Biomarker" UI item doesn't default to the first PARAMCD that is filtered to which is CRP. so a validation error is thrown however in the study app the module behavior is different. for example, the first PARAMCD in the list is ALBUM so alphabetically before ALT. after filtering in the manner described "What happened" section above and navigating to boxplot, it produces a plot for ALT which is the first PARAMCD selected in the filtered PARAMCD. I updated the "What happened" section of this issue. |
removed priority since you think it's a bigger issue with teal itself and may be handled in a current refactoring focus area. |
Acceptance Criteria
Possible solution from discussion
|
Note to consider when working on the issue: |
Note from discussion:
|
What happened?
"Select Biomarker" menu does not refresh do display all biomarkers available in data after filter panel filter on PARAMCD is removed.
Manifested in study data we are using to test upversioning and can replicate in teal.gallery app as well but there is different behavior as far as the modules producing a plot. none of the teal gallery app plots are produced if ALT is filtered out as a first step. however see below for what happens in the study data app we are using for testing.
Steps
box plot throws validation error. this is actually the sample app behavior. the study app produces a boxplot of ALTsessionInfo()
Relevant log output
Code of Conduct
Contribution Guidelines
Security Policy
The text was updated successfully, but these errors were encountered: