View source: R/cell_bar_plot.R
| cell_bar_plot | R Documentation |
Creates stacked bar charts to visualize tumor microenvironment (TME) cell fractions. Supports batch visualization of deconvolution results from methods such as CIBERSORT, EPIC, and quanTIseq.
cell_bar_plot(
input,
id = "ID",
title = "Cell Fraction",
features = NULL,
pattern = NULL,
legend.position = "bottom",
coord_flip = TRUE,
palette = 3,
show_col = FALSE,
cols = NULL
)
input |
Data frame containing deconvolution results. |
id |
Character string specifying the column name containing sample identifiers. Default is "ID". |
title |
Character string specifying the plot title. Default is "Cell Fraction". |
features |
Character vector specifying column names representing cell types to plot. If NULL, columns are selected based on 'pattern'. Default is NULL. |
pattern |
Character string or regular expression to match column names for automatic feature selection. Used when 'features' is NULL. Default is NULL. |
legend.position |
Character string specifying legend position ("bottom", "top", "left", "right"). Default is "bottom". |
coord_flip |
Logical indicating whether to flip plot coordinates using 'coord_flip()'. Default is TRUE. |
palette |
Integer specifying the color palette to use. Default is 3. |
show_col |
Logical indicating whether to display color information. Default is FALSE. |
cols |
Character vector of custom colors. If NULL, palette is used. Default is NULL. |
A ggplot2 object representing the stacked bar chart.
Dongqiang Zeng
set.seed(123)
input_data <- data.frame(
ID = paste0("Sample", 1:10),
Cell_A = runif(10, 0, 0.4),
Cell_B = runif(10, 0, 0.3),
Cell_C = runif(10, 0, 0.3)
)
cell_bar_plot(input = input_data, id = "ID", features = c("Cell_A", "Cell_B", "Cell_C"))
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