Closed PengNi closed 5 years ago
You should not consider junction motif. The preferred setting depends on your goal. Do you want to cluster different isoforms or not?
EDIT: fixed a typo
Fwiw, I don't consider junction motifs in IsoSeq3 cluster.
@lh3 , I just intend to use pairwise alignment to do self-correction of the raw reads.
@PengNi I think you can use a setting similar to IsoSeq3. @armintoepfer what setting are you using?
Just use defaults with -k 15 -w 5. Make sure you don't cluster anything that has larger gaps.
Okay, thank you. I'll have a try.
Hi Heng,
Can minimap2 be used to find overlaps between long RNA reads (e.g. PacBio Iso-seq, Nanopore 2D cDNA-seq and Direct RNA-seq reads)? Should I consider splice/junctions when I do this?
Thank you in advance! Peng