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Thanks for creating and maintaining dnaapler! It's running fantastically well. I had a feature request:
Is your feature request related to a problem? Please describe.
I am running dnaapler all ... as the input contains both plasmids and genomes.
dnaapler outputs fasta headers in the format {contig_name} rotated=True. I want to know which gene (dnaA, repA, etc) was used to reorientate which sequence.
Describe the solution you'd like
The information is captured as it's present in *_summary.tsv file. Fingers crossed this isn't a big ask
Describe alternatives you've considered
NA
Additional context
NA
Thanks!
The text was updated successfully, but these errors were encountered:
Thanks for creating and maintaining dnaapler! It's running fantastically well. I had a feature request:
Is your feature request related to a problem? Please describe.
I am running
dnaapler all ...
as the input contains both plasmids and genomes.dnaapler
outputs fasta headers in the format{contig_name} rotated=True
. I want to know which gene (dnaA, repA, etc) was used to reorientate which sequence.Describe the solution you'd like
The information is captured as it's present in
*_summary.tsv
file. Fingers crossed this isn't a big askDescribe alternatives you've considered
NA
Additional context
NA
Thanks!
The text was updated successfully, but these errors were encountered: