Hi
This is Bartek Tomiczek form University Collage London. I am trying to  
make a genome alignment with:
-rwxr-xr-x 1 bartek bartek  3858328 Nov 11  2009 progressiveMauve
-rwxr-xr-x 1 bartek bartek  2901448 Nov 11  2009 mauveAligner
form the command line version for linux. Since the visual interface is  
working fine for me the command line is constantly exiting with the  
error:

attempt 1:

-rw-r--r-- 1 bartek bartek   372948 Nov 11  2009 mauve_user_guide.pdf
-rwxr-xr-x 1 bartek bartek  3858328 Nov 11  2009 progressiveMauve
-rwxr-xr-x 1 bartek bartek  2901448 Nov 11  2009 mauveAligner
-rwxr-xr-x 1 bartek bartek      855 Nov 11  2009 Mauve
-rw-r--r-- 1 bartek bartek     3563 Nov 11  2009 README
-rw-r--r-- 1 bartek bartek    18332 Nov 11  2009 COPYING
-rw-r--r-- 1 bartek bartek   422194 Nov 12  2009 Mauve.jar
-rw-r--r-- 1 bartek bartek    31510 Nov 12  2009 ChangeLog.html
drwxrwxr-x 2 bartek bartek     1024 Nov 29 13:22 linux-x64
drwxrwxr-x 2 bartek bartek     1024 Nov 29 13:22 ext
-rw-r--r-- 1 bartek bartek    19760 Nov 29 14:19  
Sp.may2011.extras_mito.fasta
-rw-r--r-- 1 bartek bartek    84856 Nov 29 14:20  
Sp.may2011.extras_mito.fasta.sslist
-rw-r--r-- 1 bartek bartek 12531568 Nov 29 14:21 jb50contigs.fa
-rw-r--r-- 1 bartek bartek 52296828 Nov 29 14:21 jb50contigs.fa.sslist
[bartek@jb-analysis1 mauve_2.3.1]$ mauveAligner -- 
output=jb50vsSpmito.mauve --output-alignment=jb50vsSpmito.alignment  
jb50contigs.fa Sp.may2011.extras_mito.fasta
-bash: mauveAligner: command not found
[bartek@jb-analysis1 mauve_2.3.1]$ ./mauveAligner -- 
output=jb50vsSpmito.mauve --output-alignment=jb50vsSpmito.alignment  
jb50contigs.fa Sp.may2011.extras_mito.fasta
Sequence loaded successfully.
jb50contigs.fa 12304601 base pairs.
Using weight 17 mers for initial seeds
Creating sorted mer list
Create time was: 8 seconds.
0%..1%..2%..3%..4%..5%..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%..Starting with 0 MUMs
Eliminating overlaps yields 0 MUMs

*** ERROR ***  Clust::SetLeafCount(0)

attempt 2:

[bartek@jb-analysis1 mauve_2.3.1]$ ./mauveAligner -- 
output=jb50vsSpmito.mauve --output-alignment=jb50vsSpmito.alignment  
jb50contigs.fa jb50contigs.fa.sslist Sp.may2011.extras_mito.fasta  
Sp.may2011.extras_mito.fasta.sslist
Sequence loaded successfully.
jb50contigs.fa 12304601 base pairs.
Sequence loaded successfully.
Sp.may2011.extras_mito.fasta 6835866 base pairs.
Using weight 17 mers for initial seeds
Sorted mer list loaded successfully
Sorted mer list loaded successfully
Segmentation fault

attempt 3:

[bartek@jb-analysis1 mauve_2.3.1]$ ./progressiveMauve -- 
output=jb50vsSpmito.mauve jb50contigs.fa Sp.may2011.extras_mito.fasta
Storing raw sequence at /tmp/rawseq21551.000
Sequence loaded successfully.
jb50contigs.fa 12304601 base pairs.
Storing raw sequence at /tmp/rawseq21551.001
Sequence loaded successfully.
Sp.may2011.extras_mito.fasta 6835866 base pairs.
Using weight 17 mers for initial seeds
Sorted mer list loaded successfully
Sorted mer list loaded successfully
Caught signal 11
Cleaning up and exiting!
Temporary files deleted.

In all of the above examples the output file is produced but is empty.  
Do I need any additional software or am I running it in a wrong way ?
Please help me with this problem or give the contact to a person that  
can help.

Bartlomiej Tomiczek
Department of Genetics, Evolution and Environment
University College London
Darwin Building
Gower Street
London WC1E 6B
United Kingdom


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