Open gnilihzeux opened 2 years ago
I am afraid not, the current version of CIRI-long does not generate reads alignment results.
So, whether if I could generate those using your strategy in the paper ?
Cleaned reads were aligned to the mouse genome (GRCm38) version M20 (Ensembl 95) using minimap2 (ref. 45)
with the ‘–x splice’ option.
BTW, is it a better option using sequences in xxx.cand_circ.fa
instead of cleaned reads ?
Thanks.
Yes, you could use minimap2 to align cand_circ.fa to the reference genome. The result should be slightly different from the final collapsed output, but should still be enough for visualizing circRNA isoforms.
Well, it might be better if I just use reads in xxx.reads
to align xxx.cand_circ.fa
to the reference genome.
Hi, is there any option to save mapped reads? So, we could display the circRNA reads on IGV.