I have 2 batches of chip-seq samples:
(A) One biological SE replicate
This batch, actually, consists of 4 SE Chip-seq samples - one treatment, one control, both have IP controls. All are SE sequenced at a lab A
(B) Two biological PE replicates
This batch consists of 8 PE Chip-Seq samples - 2 treatment, 2 controls, all have IP controls. All are PE sequenced at a lab B.
The idea is to establish differential binding between the treatment and the controls. I plan to use macs and diffbind but I am open to suggestions.
My first specific question is how to treat the PE samples. I see 3 options:
(1) Treat all forward and reverse reads as SE reads
(2) Take just the forward or the reverse reads
(3) Treat each PE sample as, essentially, 2 technical replicates (one consisting of forward reads, one of reverse)
I find (3) intuitively attractive but, again, I am open to suggestions. If I go for it than the model would need to introduce 2 additional factors - one accounting for the technical replicates, another for the batch effect. So far I have dealt with batch effects only - I presume that adding additional factor shall be straight-forward but, please, let me know if there are things that I need to pay attention to.
Thanks, but I meant not merging the reads themselves but, rather, merge, the two read files and treat the reads in the merged file as being all SE reads. The individual reads will stay as they are. Apologies for the confusion - will edit the question