Closed tongyin121 closed 6 months ago
Hello, you need to manually curate it. For example, extract the sequence with extension to its flanking for a certain distance, ie. 1000bp, then blast your genome and see if the alignment is only on your candidate TE or extends further out.
Hello, during the use of EDTA, I found that many MITE transposons are enriched in certain regions of the genome and belong to the same TE family (TE_00001032#MITE/DTM). The sequence is TTGCCTTTGAATTTCGGGTGATCTCTCTTGAGCATGTATGCTTCTGCTACTTGTTCTACATCAGACTTCTTCCGCAAACGGCGAAACGCTTTGACTCGGTGAGTTTCGCGGCATTCCGACTTCGATGCCCCAAATTACC. I would like to ask how to verify the validity and accuracy of the annotation results?