Depends on your library type. What is the orientation?
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Are there any existing tools to artificially flip mate-pair libraries from rf to fr?
Edit
I really just need to reverse complement both libraries to make it fr right? fastx toolkit has a reverse-complement tool. I am trying that out now.
Correct, you only need to reverse complement all of your reads.
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Just curious, are these lexogen libraries that generate reads in a strand orientation opposite to the genomic reference?