Comments (3)
Hi Noah,
I am surprised. If you have annotated using prokka on default(ish) settings there shouldn't be any issues. That warning appears if the first field in the GFF3 annotation lines does not match the names of the contigs at the bottom of the file. Which version are you using? Could you send me a few example files for me to test? I have just pushed a new version and it maybe a bug I have introduced.
All the best,
Sion
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Hi Sion,
I just sent you an email containing the files that caused the error. They were annotated using prokka version 1.14.6 and I attempted to run PIRATE version 1.0.3.
Best,
Noah
from pirate.
Hi Noah,
Having looked at the files there is an obvious discrepancy between annotation and fasta headers for contig '0'. In the prokka GFFs contig 0 has been renamed to SEQ in the annotation line (col 1). This is most likely due to the your contig naming scheme having 0 as a fasta header which maybe interpreted as binary 0 (empty) by some programs in prokka.
In short, this isn't a PIRATE issue but one caused by the input being non-standard. If you rename the contig headers starting from 1 and reannotate them you shouldn't have an issue.
All the best,
Sion
from pirate.
Related Issues (20)
- Confused with terminology/output HOT 1
- extract_feature_sequences.pl failed HOT 2
- error observed during "aligning all feature sequences" HOT 2
- Missing genome in output HOT 12
- Output gene sequences to run gene alignment separately HOT 4
- PIRATE_plots.pdf created by plot_summary.R HOT 1
- Error after MCL clustering step HOT 5
- How do you tell which gene families are single-copy or multi-copy? HOT 2
- Feature request: Option to include original IDs and annotations in fasta headers for align_features_sequences script HOT 2
- Average_dose =1 is appropriate to determine whether a gene family is a single copy? HOT 1
- - ERROR: link_clusters.pl failed. HOT 1
- Undefined subroutine &main::translate called HOT 2
- Error when running PIRATE MCL process
- For some single loci, a gene family but for others not. HOT 1
- problem in installation HOT 9
- Bump version in new release HOT 4
- Missing output files and coregenom files HOT 3
- Running on large dataset HOT 2
- stuck at threshold 60 during MCL clustering HOT 3
- PIRATE.pangenome_summary.txt HOT 6
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