Hi Brianna,
It looks like you're using version 2.3.1 of Mauve to align some 2Gbp+
mouse genomes. There was an unfortunate bug in that release which
prevented the alignment of such large genomes. The snapshot releases
available here should have that fixed:
http://gel.ahabs.wisc.edu/mauve/snapshots

Also be aware that the alignment is likely to require a computer with a
lot of memory, probably 50-100GB of RAM to align mammalian genomes. 

Best,
-Aaron

On Thu, 2013-09-12 at 15:17 -0400, Brianna Flynn wrote:
> Hi there,
> I am new to Mauve, but it has come highly recommended to me instead of
> the aligner I was using previously. All I want to start with is
> aligning 2 genomes and I used the progressiveMauve GUI according to
> the directions on the source page. I got the following error from the
> computer:
> 
> 
> OS name is: Linux arch: amd64
> trying path /opt/mauve_2.3.1/progressiveMauve
> Executing: 
> /opt/mauve_2.3.1/linux-x64/progressiveMauve
> --output=/data2/indices/peromyscus/peroDraftVmm10_progMauve_def
> --output-guide-tree=/data2/indices/peromyscus/peroDraftVmm10_progMauve_def.guide_tree
>  
> --backbone-output=/data2/indices/peromyscus/peroDraftVmm10_progMauve_def.backbone
>  /data2/indices/peromyscus/deermouse.20121127.agp.fa 
> /data2/indices/mm10/mm10.fasta 
> Storing raw sequence at /tmp/rawseq44553.000
> Sequence loaded successfully.
> /data2/indices/peromyscus/deermouse.20121127.agp.fa 2820775490 base
> pairs.
> Storing raw sequence at /tmp/rawseq44553.001
> Sequence loaded successfully.
> /data2/indices/mm10/mm10.fasta 2730871774 base pairs.
> Using weight 21 mers for initial seeds
> Creating sorted mer list
> Create time was: 1664 seconds.
> Creating sorted mer list
> Create time was: 1384 seconds.
> 0%..6%..7%..8%..9%..10%..
> 11%..12%..13%..14%..15%..16%..17%..18%..19%..20%..
> 21%..22%..23%..24%..25%..26%..27%..28%..29%..30%..
> 31%..32%..33%..34%..35%..36%..37%..38%..39%..40%..
> 41%..42%..43%..44%..45%..46%..47%..48%..49%..50%..
> 51%..52%..53%..54%..55%..56%..57%..58%..59%..60%..
> 61%..62%..63%..64%..65%..66%..67%..68%..69%..70%..
> 71%..72%..73%..74%..75%..76%..77%..78%..79%..80%..
> 81%..82%..83%..84%..85%..86%..87%..88%..89%..90%..
> 91%..92%..93%..94%..95%..96%..97%..98%..99%..100%..
> done.
> using default bp penalty: 219592
> using default bp estimate min score: 658776
> Starting with 27926135 multi-matches
> Computing genome content distance matrix...
> 
> 
> 
> 
> Genome conservation distance matrix: 
> 0 0.769011
> 0.769011 0
> 
> 
> Writing guide tree
> to /data2/indices/peromyscus/peroDraftVmm10_progMauve_def.guide_tree
> reading tree...
> initializing alignment tree...
> matches[matchI - 1]->Length(0) = 2820775490
> matches[matchI - 1]->LeftEnd(0) = 1
> oh skeethockey mushrooms
> matches[0]->Length(0) = 2820775490
> matches[0]->LeftEnd(0) = 1
> oh skeethockey mushrooms too
> matches[matchI - 1]->Length(0) = 2730871774
> matches[matchI - 1]->LeftEnd(0) = 1
> oh skeethockey mushrooms
> matches[0]->Length(0) = 2730871774
> matches[0]->LeftEnd(0) = 1
> oh skeethockey mushrooms too
> Constructing seed occurrence lists for repeat detection
> terminate called after throwing an instance of
> 'std::ios_base::failure'
>   what():  failed mapping file: Invalid argument
> Exited with error code: 134
> 
> 
> 
> 
> I would sincerely appreciate any advice that anyone can offer about
> what the code means or if there is something about my input sequences
> that could be mucking things up. They are both FastA files so I
> thought they would be fine.

> 

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

http://darlinglab.org
twitter: @koadman



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