Hi all! I'm creating a variant calling workflow/tutorial for biology students with no background in informatics, using almost exclusively the Galaxy platform tools.
Now, I'm aware that I can easily teach them to run Rstudio, install GATK using the shell and run the commands. However I'm being asked to avoid anything related to CLI usage for fresh students, besides I'm not that proficient in that myself.
I could not find implemented tools for creating a sequence dictionary from the ref-genome, updating the known-sites.vcf and index according to the ref-genome Galaxy uses, and application of BQSR. Are there any tools that perform any of the above mentioned processes?
In another post in this platform 6 yrs ago I read that this step might even be neglictible, and depends on the variant calling tool (in the case of Galaxy is Lofreq).
Thanks for your time and your knowledge!
galaxy
bqsr
vcf