I found several transposase genes in a bacterial assembly and I now want to determine the size of the insertion sequence. In literature I read that transposons are usually flanked by inverted repeats (>9 bp) and direct repeats.
However, depending on which parameters I use with the tool below (max size inverted repeat or max distance between repeats) it results into many different sized inverted repeats/palindromes. So at the moment I am still not quite sure how to define where my transposon starts and where it ends.
http://emboss.bioinformatics.nl/cgi-bin/emboss/palindrome
Has anyone done something similar and used the same tool or a different one?