This program parses the delta alignment output of nucmer and displays the coordinates, and other useful information about the alignments.
There is also an optional final column (turned on with the "Annotate" parameter) that will contain some 'annotations'. The Annotate option will annotate alignments that represent overlaps between two sequences. Sometimes, nucmer will extend adjacent clusters past one another, thus causing a somewhat redundant output, this option will notify users of such rare occurrences.
The Percent Coverage and Sequence Length options are useful when comparing two sets of assembly contigs, in that these options help determine if an alignment spans an entire contig, or is just a partial hit to a different read. The Merge option is useful when the user wishes to identify sytenic regions between two genomes, but is not particularly interested in the actual alignment similarity or appearance. This option also disregards match orientation, so should not be used if this information is needed.
Options::
-b Merges overlapping alignments regardless of match dir or frame and does not display any
identity information.
-d Display the alignment direction in the additional FRM columns
-I Set minimum percent identity to display
-L Set minimum alignment length to display
-o Annotate maximal alignments between two sequences, i.e. overlaps between reference and query
sequences
-q Sort output lines by query IDs and coordinates
-r Sort output lines by reference IDs and coordinates