This site is now read-only. You can find our new documentation site and support forum for posting questions here.
Be sure to read our welcome blog!
Variant detection in RNAseq: when to merge samples
Hi, I have followed the recommendations for my RNAseq variant search as outlined here:
Since I am pretty new to the gatk world, silly questions are bound to emerge. Anyway, I have followed the linked Best Practice and are in the process of doing BaseRecalibration now. I have treated my four lines individually, meaning that alle the processes so far have been done individual by individual. My question is whether I have done this correctly - by treating the individuals separately up to now?
Since I am looking for snps, I assume that at one stage I need to merge them together, but should I have done that at an earlier stage?
Feedback/comments are greatly appreciated.