I wanna see big picture and management of RNA-seq data like
1. quality of read: base calling, length of read,.......
2 screening: contamination, mismatch criteria,.........
3......
I have read research paper but do not understand well like it's very depend on researcher's criteria
I will appreciate it if reason of which step is discussed
and ready-to-use software for analysis is good enough. Do I need to learn about Linux things
RNA-seq beginner
thank you in advance