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README

Vincent de Boer1, Xiang Zhang2

The goal of segment_me_label_free is to quantitate cell numbers from high-content microscope images using only the image. We implement this for Bright-field label-free images and it does not require a training dataset.

To run the pipeline, we have a Shiny app that loads the bright field and is used to establish the cell size. This is important, because cell size is the variable that is used to optimize the parameter automation. We also have a function that takes as input the image and the cell size. The function returns the cell number and their xy position.

In the github, we also have all code organized in quarto note book that generates all data plots and tables from the paper.

Installation

Install all the below packages to be able to run the functions and regenerate the plots

#required image analysis packages
install.packages("BiocManager")
BiocManager::install("EBImage")
install.packages(c("imager", "imagerExtra", "magick"))

#required data stats and plotting packages
install.packages(c("spatstat", "deldir",  "mclust"))

#required standard tidy and base R packages
install.packages(c("pipeR", "tidyverse"))
install.packages(c("furrr", "future"))
install.packages("fs")
install.packages("here")

#used additionally in paper data figures and notebook
install.packages("geomtextpath", )
install.packages("gt")
install.packages("ggdist", "ggforce", "dbscan")
install.packages("jsonlite")
install.packages("NCmisc")
install.packages("devtools")
devtools::install_github("inbo/inborutils")

#required for shiny app
install.packages(c("sf", "bslib", "shiny", "shinyWidgets"))

Download zenodo data

The images can be downloaded from Zenodo:

#create data directory in  your top project directory
# In my case this is:
my_root_folder <- 
  "/Users/vincentdeboer/Documents/R"
my_project_folder <- 
  "segment_me_label_free"
my_data_folder <- "data"

fs::dir_create(here::here(my_data_folder))

#download all C2C12 and THP1 images from zenodo
inborutils::download_zenodo("10.5281/zenodo.11191023", 
                            my_data_folder)

# unzip c2c12
unzip(zipfile = 
        here::here(my_data_folder, 
                   "20221207_1700_gt_C2C12.zip"),
      exdir = here::here(my_data_folder, 
                         "20221207_1700_gt_C2C12"))

# unzip THP1
unzip(zipfile = 
        here::here(my_data_folder, 
                   "20231116_1300_mm_THP1.zip"),
      exdir = here::here(my_data_folder, 
                         "20231116_1300_mm_THP1"))

Shiny app

Open the shiny app in Rstudio, by opening the app.R file and click Run App. You can upload your image, or used the provided images. If using the default images (C2C12 or THP1), make sure they are in the correct folder (see download chunk above). Follow the three steps as described in the figure below.

It is recommended to draw at least 20 polygons. The average cell size is automatocally calculated.

shiny_example

shiny_example

Pipeline master function

Set the two input variables filepath and cell_size_target:

#set the filepath of your file (here we use one of our images (also available on github))
filepath <- here::here("inst", "extdata", "20221207_1700_gt_C8_EXP4_BF.tif")

#set the cell size target
cell_size_target <-  223 #pixels

Run the master function:

PLEASE NOTE that iterating over the parameter set can take a long time. It depends on processor speed and parallization. The iteration is parallelized using furrr:future_pmap with default 10 workers.

segmented_image <- segment_my_image(filepath, cell_size_target)

# print the number of identified cells
segmented_image$n
#> [1] 1444.273
#print the xy positions for an optimal solution
segmented_image$xy %>% plot()

Footnotes

  1. Wageningen University, Human and Animal Physiology ↩

  2. Wageningen University, Human and Animal Physiology ↩