Hi Everyone,
I have few RNA-SEQ samples from diseased(8) and normal patients(5). I want to look for my subset of genes(around 80 genes), how does splicing varies in these patients in my subset of genes. I used STAR to align the raw fastq reads.
What software can I use to find whether my subset of genes, differ in splicing in 2 cases;diseased and normal?
Is DEXSeq a good start?
Hope to hear from you
Thanks