Versions Compared

Key

  • This line was added.
  • This line was removed.
  • Formatting was changed.
Table of Contents

...

  1. Open RStudio (you can type it in the Windows search bar)

  2. Create a new R script: ‘File’ → “New File” → “R script”

  3. Save this script where your samples folders are (‘File’ → ‘Save’). These should be on your H or W drive. Save the script file as scrnaseq.R

In the following sections you will be copying and running the R code into your scrnaseq.R script.

Cell Ranger (and nfcore/scrnaseq) generates a default folder and file output structure. There will be a main folder that contains all the sample subfolders (NOTE: this is where you must save your R script). Each sample folder will have an ‘outs’ subfolder. This ‘outs’ folder contains a ‘filtered_feature_bc_matrix’ folder, which contains the files that Seurat uses in its analysis.

If you have already created this script in a previous session, you can just re-open it by browsing to the location (somewhere in your mapped H drive, probably) and double clicking on it.

2b. Set your working directory

...

You can manually set your working directory in RStudio by selecting ‘Session' -> 'Set working directory' -> 'Choose directory'. Choose the same directory as you saved your scrnaseq.R script, previous section. This will output the setwd(...) command with your working directory into the console window (bottom left panel). Copy this command to replace the default setwd(...) line in your R script.

...