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By default the agat_convert_sp_gxf2gxf.pl output is GFF3. So you have GFF file. You need an extra step to run the GFF to GTF conversion and it should be fine. If you use AGAT >= 1, you can make it in one command: |
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Normalement AGAT n'ajoute pas de tag tel que "cds_start_NF" "mRNA_start_NF". Ca devait être dans un des deux fichiers que vous avez mergé. Pour ce qui est de la dernière commande je ne comprends pas pourquoi le fichier de sortie fonctionne. Tout ce que vous avez fait c'est enlever les attributs "tag" de la 9em colonne, mais je pense pas qu'il est ce type d'attribut. Utilisez AGAT >=1.0.0 |
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Bonjour |
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Hello there
I'm trying to make a custom GTF by merging a standard GTF with a handmade one. The handmade one which contains reannotated transcript, lakes level1 info that are present in the standard GTF. I have merge my two GFT files (using either the cat function of AGAT merge) and than sort the merge GTF using agat_convert_sp_gxf2gxf.pl. However, when I want to use it in cellranger-arc to creat a genome file, I got: "Property 'transcript_id' not found in GTF line XXXX" enven if this line do contains the transcript-id. But I realized that there is a difference between pre processed and post processed GTF by AGAT: the bracket arount the ID have vanished (eg: transcript_id=ENSRNOT00000093111 instead of transcript_id="ENSRNOT00000093111"). Is there a way to get them back, I beleive cellranger-arc love them ?
Best
David
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