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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