Hi Joe,

First of all, my apologies for getting back to you so late!  A
deadline that just passed kept me occupied the entire week...

Second, thanks a lot for replying to an old posting of mine -- that is
very much appreciated!


On Fri, Jul 15, 2016 at 7:17 AM, Joseph Fass <joseph.f...@gmail.com> wrote:
> Raymond, you've probably figured this out already, but since I was looking
> for discussion of these files, I'll answer your email. The SNP file doesn't
> address gaps, doesn't depend on the contig mover. The three fields for every
> genome represent the contig name (the fasta header line of the sequence
> containing the position of the SNP), the position in that particular contig
> (i.e. 1-based position of the SNP in that particular fasta entry), and the
> position in the whole genome (i.e. if you concatenated all contigs in order
> together into one sequence, what would be the coordinate of the SNP). This
> last obviously applies to a "draft" or multi-chromosomal genome that
> contains multiple fasta entries in one file; if you're dealing with a single
> chromosome, then the "position in contig" and "genome-wide position" will
> match.


Unfortunately, I didn't figure out what you mentioned here.  The
project that I was using Mauve for is "on hold" for reasons completely
unrelated to Mauve.  I still would like to get back to it some day.

Thank you for this explanation!  It is useful information to know
whenever I return to that project and I hope it is useful for others
reading the list.

Thank you!

Ray

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