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Thank you @Juke34 for putting the time and effort into developing and documenting this extremely useful software! I couldn't find anywhere so am asking here:
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Hi @svigneau, thank you for your questions
Excepted the mention in the log generated while running a script no. Moreover this is not really explained...
Actually this not really used yet... I wanted at some point to implement something that use this information when AGAT needs to create a missing parent feature. What really matter is to set the feature types in their proper category level1, level2, level3 respecting the relationships you expect in your file.
This is used only to provide information to the user if the feature types meet in the file follow the sequence ontology (SO) or not. As in GFF3 format the feature types are constrained to be part of the SO, it helps the user to see if his file is fully compliant or not. If not, the user may modify the feature types to match an existsing one or apply to add a new term in SO.
The best and only way should be to have the correct relationships set in the file. e.g. using ID/Parent attributes as for GFF, or using transcript_id and genet_id as in GTF or to use a common attribute that is shared by all features belonging to the same record. |
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Hi @svigneau, thank you for your questions
Excepted the mention in the log generated while running a script no. Moreover this is not really explained...
I should definitly add some information in the doc.
Actually this not really used yet... I wanted at some point to implement something that use this information when AGAT needs to create a missing parent feature. What really matter is to set the feature types in their proper catego…