I am beginner and want to know how people usually perform single cell RNA Seq Analysis on clusters - RStudio GUI on HPC or RScript execution on HPC terminal.
I heard that one way to do is - write script in a section, execute, check errors, execute and then finally compile all together to execute final one. Same can be applied for other samples or cells. Also, is this the way to develop a new pipeline?
Any comments would be appreciated.
If you have a HPC then you must have folks that administer that HPC. You can work with them to see if any of this is already available on your cluster (there may already be RStudio etc). You could then ask them to install the necessary packages (if they are not already present, you won't likely be the only person using scRNA at your institution). This may lead to a much more efficient/pleasant user experience.