Closed splaisan closed 7 months ago
Hi @splaisan,
I’ll come back with a more lengthy explanation tomorrow (it’s late in Australia), but I have just the tool for you I think :)
Hi George,
Both dnaapler and pharokka rock, they need more exposure (you should consider making a bioXiv paper of some kind to promote your work !
I ran dnaapler phage based on your very clear doc and it seems to have worked like a charm.
I will most likely drop circlator fixstart
from now on and use dnaapler
for all my reorientation needs.
Finishing an assembly with reorientation is a real must, too often I see random circles published and very hard to compare by eye.
Thank you so much for your nice work and clear tools.
Thanks @splaisan for you very kind words - I am trying to get Dnaapler published at JOSS, hopefully won't be too long :)
Another thing is that you can actually run Dnaapler within pharokka if you use --dnaapler
- the reoriented phage is in the output directory.
If you do bacterial assemblies too, you may be interested in my tool Hybracter (https://github.com/gbouras13/hybracter) - a preprint for this one is coming very soon, and I'd love feedback if you try it out.
George
Thanks George,
I indeed saw the option after receiving your message. I will include it next time. I did not know yet what dnaapler was then.
I can easily try Hybracter as I just performed bacterial assemblies which I rotated with circlator. I will redo this step and let you know.
cheers
Hi George, All,
disclaimer: sorry but I am not a bacteriologist nor a virolog ;-)
I do not find 'terminase' genes in my circularStx- phage assemblies although they are described in Pinto et al 2021 for this usage! Is this normal in a non-integrated form or is it due to flye
I usually use
circlator fixstart
to put DnaA at +1 in bacterial assemblies and would like to also show nice maps for my phages.Do you have a recommendation for the choice of the first gene to show on a bacteriophage map? Is the first shiga gene a good option?
thanks for your feedback and knowledge