Closed splaisan closed 1 year ago
Maybe I can use --replicons and a minimalist table with only 'original sequence id' and the same 'new sequence id' to force the names to the original flye contig names?! Just found the comment in the doc😅 and will try this tomorrow Maybe an option '--keep_names' with defaut to false could help here for other people with the same issue.
Hi @splaisan,
If you only would like to keep the original contig IDs, then simply setting --keep-contig-headers
should work.
There are some other parameters that might be interesting/helpful. You can find a full description here: https://github.com/oschwengers/bakta#usage
Please, do not hesitate to ask, if there are any further questions.
How could i mis this one, i definitely have to read the usage more carefully 🤣
You're welcome ;-)
Dear Oliver,
I ran bakta using your latest docker (bakta 1.8.2) and found when visualising various results in IGV that the original Flye contigs had been renumbered/renamed by bakta in the annotation files to arbitrary 1/2/3 indices.
Is this intended and how can I prevent it? I have mapped data which I want to show side by side with annotations and this is not going to work well.
Thanks for your feedback
input fasta assembly:
bakta fna file