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Hi,
I got somewhat lost in the parameters of RIPseeker. I would like to do peak calling on the data produced with TruSeq Smalll RNA Illumina protocol. It is a stranded library prep protocol - sequencing reads from read 1 map to the antisense strand and those from read 2 map to the sense strand.
Should I use
reverseComplement = TRUE or FALSE
strandType = "+", "-", or "*"
Thank you!
Did you ever arrive at a solution?
Would also love an answer to this. The Truseq prep protocol uses --fr-stranded technology (if that helps).