there were some genes from the reference genome not being recognized by mitofinder, so I modified mitohifi_v2.py code at lines 236 and 286 to include the --new-genes parameter at the mitofinder execution code. (base on https://github.com/marcelauliano/MitoHiFi/issues/11). However, motifhifi could not generate final_mitogenome.fasta and final_mitogenome.gb.
Attached are the log files and a list of files in the result directory.
Hi,
Thanks for the excellent tool.
I am trying to run mitohifi with raw reads of a plant genome using the following command:
mitohifi_v2.1.py -r Kalea.merged.ccs.contaminationfree.fasta -f MT361980.1.fasta -g MT361980.1.gb -t 40 -o 1 1>MITOHIFI1.LOG 2> MITOHIFI2.LOG
there were some genes from the reference genome not being recognized by mitofinder, so I modified mitohifi_v2.py code at lines 236 and 286 to include the --new-genes parameter at the mitofinder execution code. (base on https://github.com/marcelauliano/MitoHiFi/issues/11). However, motifhifi could not generate final_mitogenome.fasta and final_mitogenome.gb.
Attached are the log files and a list of files in the result directory.
Any idea what can cause the problem?
Thanks, Mojtaba
lift_files.txt MITOHIFI1.LOG MITOHIFI2.LOG ptg000009l.annotation_MitoFinder.log hifiasm.log ptg000009l_RC.annotation_MitoFinder.log