Kindly request you share your thoughts and tutorials for RNAseq data analysis from Raw data (FASTQ files) to arrive at differentially expressed genes.
What is the best approach for pooled data? some of the posts here in the forum recommends not using pooled data but in this case i have to. so kindly share your thoughts on how to modify or alter the workflow/code/approach since i am using pooled data
Any help would be much appreciate it
Thank you for your time