Hi Norhan,
If you need programmatic access to do automated processing, you can use
the coordinates in the .backbone file to query an annotation file to get
the features at those particular coordinates. Probably
BioPython/BioPerl/BioJava or some similar API could help with annotation
parsing & queries. Keep in mind that the .backbone file uses a
concatenated coordinate system, e.g. the 1st site in the 2nd
contig/chromosome has a coordinate which is the length of the 1st + 1,
so some logic to convert to contig local coordinates will need to be
implemented.

If you just want to explore visually, you should be able to load aligned
GenBank format files into the Mauve viewer and zoom in on regions of
interest.

Best,
-Aaron

On Thu, 2015-04-02 at 00:03 +1100, Norhan Mahfouz wrote:
> Hi,
> I am currently analyzing alignment data from 50 bacterial genomes after 
> applying progressive mauve for the alignment.
> I am processing the backbone file and I was wondering how can I 
> integrate annotation information to this knowledge, for example : from 
> the backbone file seq1 and seq5 have in common a stretch of nucleotides 
> from 11658 to 11768 and 12340 to 12450 respectively - one can extract 
> the actual string of nucleotides from the xmfa file, sure
> If I am using the annotated genomes, how can I extract which genes does 
> this area belong two on each of the respective genomes??
> Your input and ideas are highly appreciated!
> regards,
> Norhan
> 

-- 
Aaron E. Darling, Ph.D.
Associate Professor, ithree institute
University of Technology Sydney
Australia

http://darlinglab.org
twitter: @koadman





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