Hi,

I am trying to align the core genes (~1000 genes) of 41 small bacterial 
genomes. However, depending on the input order I am getting a lot of 
scoring error messages or no errors.
Unfortunately I didn't find an input order for all 41 genomes which 
produces no errors.
In addition I found two sequence files where even
progressiveMauve --output=outfile seq1.faa seq2.faa
produces scoring errors while
progressiveMauve --output=outfile seq2.faa seq1.faa
does not.

I am using version 2.4.0 on Linux. In version 2.3.1 no scoring errors 
show up, but progressiveMauve gets caught in an endless loop for the 
same input orders.

What does scoring error mean?
Is there any way to predict which order of sequences will produce 
scoring errors and which doesn't?
Or even better is there a way to modify the input data to prevent the 
scoring error at all?

Greetings,

Franz Baumdicker

-------
Dr. Franz Baumdicker
Math. Institut
Eckerstr 1
79106 Freiburg

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