Open biochristmas opened 2 days ago
Hi @biochristmas
If you want to do in in a single IsoQuant run, I'd suggest to use nanopore as a datatype. However, if PacBio has a noticeably lower coverage, PacBio reads may be ignored in some cases.
Alternatively, you run IsoQuant twice and merge the resulting annotations using, for example, gffcompare.
Best Andrey
Hi @andrewprzh
I performed Isoquant twice, once with Nanopore data and once with PacBio data. Now I have two annotation files, and I tried using gffcompare to merge them, but it doesn’t seem quite right; it appears to deduplicate individual annotation files. For the software gffcompare, which is used to merge and deduplicate the results of Isoquant from two annotation files, do you have recommended commands for merging and deduplicating?
Hi I have two sets of input data, one from Nanopore and the other from PacBio. Could you please advise on the ‘--data_type’ parameter? Should I choose ‘pacbio_ccs’ or ‘nanopore’? My goal is to obtain an annotated file after annotation extension.