Dear Dr.
Thanks for your great scripts, and its helpful for my project. Now I want to filter some seqs which C-score lower than 0.5 after genome annotation. I mapped the gene models proteins to a protein database (which contained several species gene models which have been published), and I have no gff file for this protein database. So my question is how to use blast_to_raw.py if gff file for -sbed option is not available. Thanks for your help!
Is it possible to get the position information for those proteins? Then you could probably generate your own BED file, which can be formatted with just chr, start, end, geneid columns.
Dear Dr. Thanks for your great scripts, and its helpful for my project. Now I want to filter some seqs which C-score lower than 0.5 after genome annotation. I mapped the gene models proteins to a protein database (which contained several species gene models which have been published), and I have no gff file for this protein database. So my question is how to use blast_to_raw.py if gff file for -sbed option is not available. Thanks for your help!