Hi friends,
We sequenced miRNA from 12 pig samples. I did the analysis using miRDeep2 tool.
My aim is to find isomiRs for each sample. I have written a perl script to annotate isomiRs for the reads mapped to miRNA . I get the below output. The My doubt is, am I using the correct output file for the analysis? Which read count should I use miRBase.mrd or output.mrd?
I got the following folders and files
1) miRDeep2_output/dir_prepare_signature1345475348 (contains .fa, .arf, .bwt and .ebwt)
2) miRDeep2_output/expression_analyses/expression_analyses_04_03_2018_t_07_26_27
- miRBase.mrd
3) miRNAs_expressed_all_samples_04_03_2018_t_07_26_27.csv
4) miRDeep2_output/mirdeep_runs/run_04_03_2018_t_07_26_27/
- output.mrd
For future reference: Editing an original post (even without making any changes) and saving will automatically bump it to main page. No need to create duplicate postings/add fake answers on original post.
Thanks, I have made changes to the existing post itself.