Hi, I've been doing a lot of bioinformatics lately and was asked to perform variant calling on RNA-Seq data used in my lab
the thing is that I used Salmon to quantify may RNA-Seq data, and performed Differential expression analysis
now that I want to generate BAM files for the variant calling I need to use STAR
the question is, do I need to perform alignment with STAR and then quantify again with salmon,
or is it possible to just run with my DE analysis and just generate the BAM files with STAR for the variant calling?