there you go :), I upvoted harishk0201 answer myself
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hi
i aligned two whole genome using nucmer with this simple command
nucmer reference_genome.fasta query_genome.fasta
then three outputs files were created: out.delta, out.coordinates, out.tiling
Now, is there any way to know how percent of reference genome, covered by query genome?
You can use dnadiff from the MUMmer suite actually. It will generate a .report file where all the details are present.
Not as such I think, you will have to post-process one of those output files (the out.coordinates if I remember well)
there you go :), I upvoted harishk0201 answer myself
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