Closed MarionPerrier closed 7 months ago
So you need to provide a file with -f
which contains all the files you want to squeeze together. For example my_graphs.txt
:
combined_pg.fa.gz.community.0.smoothxg.gfa
combined_pg.fa.gz.community.0.smoothxg.gfa
combined_pg.fa.gz.community.1.smoothxg.gfa
combined_pg.fa.gz.community.2.smoothxg.gfa
combined_pg.fa.gz.community.3.smoothxg.gfa
combined_pg.fa.gz.community.4.smoothxg.gfa
combined_pg.fa.gz.community.5.smoothxg.gfa
combined_pg.fa.gz.community.6.smoothxg.gfa
combined_pg.fa.gz.community.7.smoothxg.gfa
combined_pg.fa.gz.community.8.smoothxg.gfa
combined_pg.fa.gz.community.9.smoothxg.gfa
Oh ok! It works like a charm now. Thank you
Hi!
I used PGGB to build a pangenome graphs of 15 assemblies. The PGGB pipeline splits the assemblies in communities, resulting in several GFA output for each communities. I would like to use odgi squeeze to combine my GFA graphs into a single one for further processing with VG.
Here is my command line:
Here is the error:
If I replace the "-f" by "-i", I then get an error "Flag could not be matched: 'i'"
What am I doing wrong? My GFA files are indeed GFAv1.
Here is an example of the smallest of them:
Odgi has been installed using conda, and the version is v0.8.4-0-g3f59d596