thanks a lot.I will try the way you said.
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I use a mature mRNA sequence (cds) to blast in an unannotated genome, because of the presence of introns, we get several exon fragments, how do I extract them and organize them into a complete cds?The genome has no gff3 files, only gbff files.
You can take your mRNA FASTA files, and map to the genome with gmap. Use the GFF3 output option.
You're not going to get anywhere with BLAST.
For a full reannotation, try Maker.
Else you could try converting your GBFF files, whatever they are.
thanks a lot.I will try the way you said.
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