Hello, I have whole genome pairwise alignments generated using Nucmer. The alignment is a table file with chromosome number, starting and end positions of all alignments between the 2 genomes (both for the reference and the query genome). Is it possible to identify inversions between the two genomes from this data?
Thanks
Have you tried
MUM&Co
1?No I haven't. But I had a look and it seems quite useful. Just one thing though, would it be suitable for detecting structural variants when comparing different species (as in the genomes in the alignment come from different species)?