Hi Mariam,
Perhaps the easiest way to do this is via the graphical interface. If
you load the final alignment generated by the contig mover in the Mauve
viewer, any unplaced contigs will appear on the right side of the draft
genome track. They will be unaligned, and therefore will not have any
similarity plot or connecting lines to the reference genome. If you
hover the mouse over one of those contigs its name will appear in the
lower right corner of the window.
If you need an automated approach you might be able to base it off of
the _contigs.tab file in the output directory, which describes what was
done with each contig at each reorder iteration.

Best,
-Aaron

On Fri, 2014-05-23 at 09:30 -0500, Mariam Iskander wrote:
> Hello, 
> 
> I am using MCM to order some contigs, and I would like to exclude the
> contigs with no ordering information associated with them. According
> to the User Guide, the contigs with no LCBs are included at the end of
> the genome, but I could not figure out where the ordered contigs end
> and the unordered ones begin. I looked through the output files and I
> couldn't find this information. Is it possible to get the list of
> contigs with no LCBs? 
> 
> Thank you very much. 
> 
> Mariam
> 
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-- 
Aaron E. Darling, Ph.D.
Associate Professor, ithree institute
University of Technology Sydney
Australia

http://darlinglab.org
twitter: @koadman



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