Hi Kevin, I hope this doesn't find you too late. Reply below...

On Wed, 2014-06-11 at 15:52 +1000, Kevin Kocot wrote:
> uqkkocot@barrine3:~> progressiveMauve --seed-family --seed-weight=11
> --backbone-output=backbone_output --output=output.mauve seq1
> Amphimedon_queenslandica_genomic_scaffolds.fa seq2
> Mnemiopsis_leidyi_genomic_scaffolds.fa seq3
> Monosiga_brevicollis_genomic_scaffolds.fa seq4
> Nematostella_vectensis_genomic_scaffolds.fa seq5
> Pleurobrachia_bachei_genomic_scaffolds.fa seq6
> Trichoplax_adhaerens_genomic_scaffolds.fa
> Exception FileNotOpened thrown from
> Unknown()  in gnFileSource.cpp 67
> Called by Unknown() 
> 
> Searching with seed pattern 111001001010100100111
> 
> Searching with seed pattern 1110101001001010111
> 
> Searching with seed pattern 1111001010101001111
> done
> Floating point exception
> 
> Thanks!
> Kevin

The FileNotOpened error message suggests that progressiveMauve wasn't
able to read one of the files you've asked it to align. Can you confirm
whether the file "seq1" exists and contains fasta sequence? If you meant
to just align the *.fa files, then the correct command-line syntax for
progressiveMauve would be to omit the seq1 seq2 etc.
Some other notes: a seed weight of 11 might be a bit small for these
genomes, probably it would be better to go with whatever
progressiveMauve selects as a default at least for a first attempt. The
--seed-family option will improve the ability to detect homology at
higher sequence divergence, but comes at the cost of speed. I am not
sure whether it will be worthwhile for the genomes you've got.

Best,
-Aaron


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

http://darlinglab.org
twitter: @koadman



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