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I installed AGAT using bioconda. I am trying to run the following: agat_sp_manage_functional_annotation.pl -gff braker1+2_combined.gtf -i genome_AA.faa.tsv -o braker.interproscan
The input GTF file is the output of the TSEBRA combiner tool that combines the predictions from Braker1 and Braker2. I am getting the error:
gff3 reader error level1: No ID attribute found @ for the feature: scf7180000002648 AUGUSTUS gene 57422 208439 . + .
gff3 reader error level2: No ID attribute found @ for the feature: scf7180000002648 AUGUSTUS transcript57422 208439 . + .
WARNING level2: No Parent attribute found @ for the feature: scf7180000002648 AUGUSTUS transcript 57422 208439 . + . ID "transcript-1"
WARNING gff3 reader: Hmmm, be aware that your feature doesn't contain any Parent and locus tag. No worries, we will handle it by considering it as strictly sequential. If you disagree, please provide an ID or a comon tag by locus. @ the feature is:
I saw other people had issues with TSEBRA output formatting, so I ran the rename_gtf.py script to clean up the gtf file but the error persists.
Hi, any reason you opened the issue in the GAAS repo rather the AGAT repo?
No worries, they are just warning. Indeed for many years Augustus and subsequent tools as TSEBRA create feature without mandatory attributes requested by the format (here the transcript feature line).
AGAT handles this perfectly well.
In such case AGAT uses a sequential approach, which means all level3 features (exon, CDS...) are llinked o the last level2 feature (transcript) met when reading the file from top to bottom.
Look at the output for the example you provided, you will see it should be fine.
Hello,
I installed AGAT using bioconda. I am trying to run the following:
agat_sp_manage_functional_annotation.pl -gff braker1+2_combined.gtf -i genome_AA.faa.tsv -o braker.interproscan
The input GTF file is the output of the TSEBRA combiner tool that combines the predictions from Braker1 and Braker2. I am getting the error:
I saw other people had issues with TSEBRA output formatting, so I ran the rename_gtf.py script to clean up the gtf file but the error persists.
Here are the top lines of the 'clean' gtf file:
Do you have any suggestions on how to fix this?
Thanks in advance!
Julia
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