Hi Hao-Ping,
Mauve Contig Mover never merges contigs, it only assigns an ordering to
contigs for which an ordering can be inferred.  If a contig has no
sequence identity to the reference genome at all, that contig is not
ordered by MCM. 

Did you paste the entire scaffold_contigs.tab file in your e-mail?  If
so, the line suggests that only one contig named "[1,4540734]" was
ordered by MCM.  Given that contig's name, I'm going to assume that the
single scaffold (contig) contains nearly all of the 4.5Mbp genome of
your organism, and the remaining 8 scaffolds in your input file are very
small.  They may not have any recognizable nucleotide-level sequence
identity to your reference organism.

Hope that helps,
-Aaron



On Tue, 2009-08-11 at 14:54 -0700, Hao-Ping Chen wrote:
> Hi there,
> 
> I currently have 9 scaffolds (about 4.5Mb) in my draft genome and
> would like to use Mauve Contigs Mover to order these scaffolds. My
> reference sequence (about 7Mb in gbk file) is from a close-related
> organism. I put all 9 scaffolds in one fasta file. The content of the
> file is as following:
> 
> >Scaffold1
> atttg.......
> >Scaffold2
> ttgcggtacc.....
> >Scaffold3
> aaattggatc.....
> 
> The output of my "scaffold_contigs.tab" is as following:
> 
> Ordered Contigs
> type    label   contig  strand  left_end        right_end
> contig  [1,4540734]     chromosome      forward 1       4540734
> 
> >From this result, it seems likely that all 9 scaffolds have been
> merged into one contig during the run. I can not obtain the
> information regarding the scaffold order in genome. Is there anyone
> can help me to solve this problem?
> 
> Thanks,
> 
> Hao-Ping
> 
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