Hi all,
i am currently using MirDeep2, i have aligned my reads on my genome. Now i try to detect the precursos thanks to this script : excise_precursors.pl
i execute this command :
However i obtain only 14 precursors for 800 reads (i think there is a problem, moreover there is no preicision about the output of this script in the doc)
If somebody have an idea... or an experience with MirDeep2
Thank you
i am currently using MirDeep2, i have aligned my reads on my genome. Now i try to detect the precursos thanks to this script : excise_precursors.pl
i execute this command :
Code:
excise_precursors.pl genome.arf reads_vs_genome.arf my_output.fa
If somebody have an idea... or an experience with MirDeep2
Thank you