I used EDTA v2.01 to identify TE. but in the genome.fasta.mod.EDTA.TEanno.gff3 check found that there are very many TE overlap area. As shown below. Do I need to process and filter these overlapping TE? Because I want to do a detailed analysis of TE in this genome. Thanks very much!
Dear Dr.Ou
hi
I used EDTA v2.01 to identify TE. but in the genome.fasta.mod.EDTA.TEanno.gff3 check found that there are very many TE overlap area. As shown below. Do I need to process and filter these overlapping TE? Because I want to do a detailed analysis of TE in this genome. Thanks very much!
Best regards