Closed:Interpreting dnadiff output
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5.9 years ago
112498262 ▴ 10

Hi,

I am trying to find unique sequences between related bacterial genomes using NUCmer and its wrapper dnadiff. The .rdiff is what I'm looking at to find gaps but I can't work out what the last 3 columns of the output mean. Is there a breakdown of the dnadiff output files?

Thanks.

genome sequence alignment • 196 views
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