Maybe both are correct as well.


At this point, you can take scaffolds and validate contig order against 
the reference.

I wrote a tool for that that utilisez MUMmer. MUMmer is an aligner for 
large sequences
and was co-published by the researchers that did the GAGE thing.

The tool is available on my github in the Ray-TestSuite project.

Example:


ValidateGenomeAssembly.sh bacterialReference.fasta 
RayOutput/Contigs.fasta Ray-assembler


This will do a lot of checks to assess the quality of the assembly, 
using the
MUMmer tool as the comparison engine.


nikos ioannidis a écrit :
> Well, if i use a reversing algorithm and reverse the short jumps
> from this :
> <--------------        --------------->
> to this :
>
> ------------><--------------
> i get diferrent results, for example for the Staphylococcus aureus of
> GAGE site with k31
>
> i get without reversing the shortjumps:
>
>
> N50 for Contigs>= 100 nt 15862
> N50 for  Contigs>= 500 nt 16024
> N50 for Scaffolds>= 100 nt108215
> N50 for Scaffolds>= 100 nt 108215
>
>
>
> and with reversing the shortjumps:
>
>
> N50 for Contigs>= 100 nt 15862
> N50 for  Contigs>= 500 nt 15862
> N50 for Scaffolds>= 100 nt 168850
> N50 for Scaffolds>= 100 nt 168850
>
> and for k21
>
> i get without reversing the shortjumps:
>
>
> N50 for Contigs>= 100 nt 30722
> N50 for  Contigs>= 500 nt 30722
> N50 for Scaffolds>= 100 nt161951
> N50 for Scaffolds>= 100 nt 161951
>
>
> and with reversing the shortjumps:
>
>
> N50 for Contigs>= 100 nt 31077
> N50 for  Contigs>= 500 nt 31637
> N50 for Scaffolds>= 100 nt 222525
> N50 for Scaffolds>= 100 nt 222525
>
>
> The main diferrence is at the scaffolds, is it normal ? what results
> are for you seems correct?
>
>
> Thank you
>
>
>
>
> On Mon, May 28, 2012 at 7:32 PM, nikos ioannidis<niioa...@gmail.com>  wrote:
>> Sorry I have made a mistake,
>> in the previous post I was talking about Short jump libraries,
>> so is there anything i need to do in order to insert these reads in the Ray?
>> Because for example in Velvet i think the user have to reverse the library
>> with some tool before,
>> while in ALLPATHSLG that is not  nesessary.
>>
>> Also about Long jump libraries the same question.
>>
>>
>> Thank you and sorry for the previous post.
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