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

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