Thank you! I ran miRanda, but the output can get really big. I used my known miRNA and looked for putative targets in the trascriptome of P. vlugaris and i got my output file, which mapped my miRNA to tons of different sequences.
Do you have any suggestion on how to process the output file in a nice way? Like to extract only matches with good scores, or something like that. How you process it usually?
Thanks again for the support!