Hi Saleh, I realize this reply is coming quite late. Hopefully it is
still useful. more below...

On Wed, 2014-06-18 at 09:43 +1000, Saleh T wrote:

> I used progressivemauve to compare two genomes each saved in the fasta
> file format. In each genome file there are more than one sequence
> corresponding to the chromosomes. I read in the manual that fasta file
> containing multiple sequences will be merged together.
> 
> 
> I have two questions:
> 
> 
> 1) Where do I find the LCBs? Running progressive generated 3 files
> (.xmfa, .bbcols, and .backbone). From reading the manual and this
> forum I had a feeling that the LCBs are located in the backbone file.
> However the backbone file has a lot of records while when I visualize
> the alignment from the mauve interface it says there are only few
> thousands LCBs, a number way low compared to the records in the
> backbone file. Could someone please clarify this?   

When using 3 or more genomes and permitting alignments among subsets of
the genomes, the LCBs can become (mathematically) ambiguous to define,
e.g. the same alignment could yield multiple alternate sets of LCBs.
Thus the LCB concept is only well-defined in the context of pairwise
alignment or core genome alignment (where only content shared by all N
genomes is aligned).

> 
> 
> 
> 2) Since my interest is on finding the LCBs, how do I go back to find
> out where these LCBs are located in the genome after the chromosome
> sequences have been merged together? Currently the coordinates seen on
> the backbone file are irrespective of the chromosome sequence.
> 

Given the aforementioned issue I think we need to know more about what
you're hoping to achieve before it's possible to suggest how to get
there with the progressiveMauve outputs.


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

http://darlinglab.org
twitter: @koadman



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