You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
I want to use Phables on stream biofilm metagenomes. I have a very intricate gfa graph obtained after MEGAHIT and during my tests Phables was able to solve only 4 case2_linear phages where several nodes are actually merged. I am wondering if I can tune some parameters to improve the performance?
I could also start from a different gfa graph. For instance in Hecatomb a Flye assembly of the contigs from my different samples is proposed: it is more doable than a cross-assembly in terms of resources and would simplify the gfa graph. I am afraid it would introduce chimeric contigs though.
The text was updated successfully, but these errors were encountered:
I want to use Phables on stream biofilm metagenomes. I have a very intricate gfa graph obtained after MEGAHIT and during my tests Phables was able to solve only 4 case2_linear phages where several nodes are actually merged. I am wondering if I can tune some parameters to improve the performance?
I could also start from a different gfa graph. For instance in Hecatomb a Flye assembly of the contigs from my different samples is proposed: it is more doable than a cross-assembly in terms of resources and would simplify the gfa graph. I am afraid it would introduce chimeric contigs though.
The text was updated successfully, but these errors were encountered: