| trelli_foldchange_boxplot | R Documentation | 
Specify a plot design and cognostics for the fold_change boxplot trelliscope. Fold change must be grouped by an emeta column, which means both an omicsData object and statRes are required to make this plot.
trelli_foldchange_boxplot(
  trelliData,
  cognostics = "biomolecule count",
  p_value_thresh = 0.05,
  include_points = TRUE,
  ggplot_params = NULL,
  interactive = FALSE,
  path = .getDownloadsFolder(),
  name = "Trelliscope",
  test_mode = FALSE,
  test_example = 1,
  single_plot = FALSE,
  ...
)
| trelliData | A trelliscope data object with omicsData and statRes results. Required. | 
| cognostics | A vector of cognostic options for each plot. Valid entries are "biomolecule count", "proportion significant", "mean fold change", and "sd fold change". Default is "biomolecule count". | 
| p_value_thresh | A value between 0 and 1 to indicate significant biomolecules for the anova (MS/NMR) or diffexp_seq (RNA-seq) test. Default is 0.05. | 
| include_points | Add points. Default is TRUE. | 
| ggplot_params | An optional vector of strings of ggplot parameters to the backend ggplot function. For example, c("ylab(”)", "xlab(”)"). Default is NULL. | 
| interactive | A logical argument indicating whether the plots should be interactive or not. Interactive plots are ggplots piped to ggplotly (for now). Default is FALSE. | 
| path | The base directory of the trelliscope application. Default is Downloads. | 
| name | The name of the display. Default is Trelliscope. | 
| test_mode | A logical to return a smaller trelliscope to confirm plot and design. Default is FALSE. | 
| test_example | A vector of plot indices to return for test_mode. Default is 1. | 
| single_plot | A TRUE/FALSE to indicate whether 1 plot (not a trelliscope) should be returned. Default is FALSE. | 
| ... | Additional arguments to be passed on to the trelli builder | 
No return value, builds a trelliscope display of fold_change boxplots that is stored in 'path'
David Degnan, Lisa Bramer
 
if (interactive()) {
library(pmartRdata)
# Transform the data
omicsData <- edata_transform(omicsData = pep_object, data_scale = "log2")
# Group the data by condition
omicsData <- group_designation(omicsData = omicsData, main_effects = c("Phenotype"))
# Apply the IMD ANOVA filter
imdanova_Filt <- imdanova_filter(omicsData = omicsData)
omicsData <- applyFilt(filter_object = imdanova_Filt, omicsData = omicsData,
                       min_nonmiss_anova = 2)
# Normalize my pepData
omicsData <- normalize_global(omicsData, "subset_fn" = "all", "norm_fn" = "median",
                             "apply_norm" = TRUE, "backtransform" = TRUE)
# Implement the IMD ANOVA method and compute all pairwise comparisons 
# (i.e. leave the `comparisons` argument NULL)
statRes <- imd_anova(omicsData = omicsData, test_method = 'combined')
# Generate the trelliData object
trelliData4 <- as.trelliData(omicsData = omicsData, statRes = statRes)
# Build fold_change box plot with statRes data grouped by edata_colname.
trelli_panel_by(trelliData = trelliData4, panel = "RazorProtein") %>% 
  trelli_foldchange_boxplot(test_mode = TRUE, 
                            test_example = 1:10,
                            cognostics = c("biomolecule count", 
                                           "proportion significant", 
                                           "mean fold change",
                                           "sd fold change"),
                            path = tempdir()
                           )
                           
                           
#####################
## RNA-SEQ EXAMPLE ##                            
#####################
# Build fold_change box plot with statRes data grouped by edata_colname.
trelli_panel_by(trelliData = trelliData_seq4, panel = "Gene") %>% 
  trelli_foldchange_boxplot(test_mode = TRUE, 
                            test_example = c(16823, 16890, 17680, 17976, 17981, 19281),
                            cognostics = c("biomolecule count", 
                                           "proportion significant", 
                                           "mean fold change",
                                           "sd fold change"),
                            path = tempdir()
                           )
}
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