Entering edit mode
14.2 years ago
Newbie
▴
40
Hi,
I have 25bp SOLiD Frag data.
Goal is to find novel small rna.
So far I have used SHRiMP2 to align the data with default parameters.
Generally what tools/method/steps are used for further downstream analysis(for e.g. remove duplicates, to remove know RNA etc.)
Thanks a lot.
I had a similar question here, about general ncRNA: Identified Potential Non-Coding Rna, And Then?
Thanks Michael, James and Shameer for your suggestions. I wish - somebody had good blog post on pipeline. Thanks for your answers and support.