RIPseeker peak calling parameters for TruSeq Samll RNA stranded library
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ofonov ▴ 10
@ofonov-12623
Last seen 7.2 years ago
Norway/Oslo

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!

 

RIPseeker RIP rna-seq • 1.0k views
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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).

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