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> From: matteo brilli [matteo.bri...@fmach.it]
> Sent: Monday, May 19, 2014 6:58 AM
> To: Boisvert, Sebastien
> Subject: technical information
> 
> 
> 
> 
> Dear Sebastien,
> 
> I started using Ray a few months together with Abyss for assemblying a paired 
> end illumina library of a genome we know little (e.g. if it is highly 
> repetitive or not, even the number of genetically different individuals is 
> not sure being impossible to cultivate
> this organism separately from its host). So, let's say we did the assemblies. 
> Now, with abyss (more or less all default params) we get larger assemblies 
> than with Ray and better N50; the main difference is the "redundancy" of 
> these assemblies. With the term
> redundancy I mean the fact that in Abyss much more than in Ray, we get some 
> of the contigs that are joined together multiple times to give the final 
> assembly. 

Can you define what you mean by redundancy ?

Do you mean that you are seeing duplicated sequences in your assembly (in this 
case, with ABySS) ?

> It is true that abyss was run for k=60 to 95 in step of 5,

I don't know what is "step of 5".

> so we have little overlapping of the same
> kmers for the two softwares, anyway where there is overlapping what I am 
> saying above is true and it is evident considering that for the abyss 
> assemblies, when I group all gene predictions based on homology at 99% 
> identity I end with N groups = 0.6 N genes,
> while in Ray doing the same the groups are 98% of the number of genes.
> 

Hypothesis: you said you have more contigs with Ray. So maybe some genes from 
your Ray assembly are
in more than 1 contigs and that generates more groups to show up.

> I don't know if the redundant part in abyss is the result of assemblying 
> errors whereas Ray is right, but I was wondering how Ray flatten this signal 
> which is present in the reads.

If you want to compare k-mer content between the 2 assemblies, you can actually 
do that with Ray:

mpiexec -n 99 \
Ray -k 31 \
-read-sample-assembly Ray-assembly.fasta \
-read-sample-assembly ABySS-assembly.fasta \
-run-surveyor \
-output Comparison-of-Ray-and-ABySS


Just be sure that Ray-assembly.fasta and ABySS-assembly.fasta are multi-line 
fasta files.

> 
> Cheers
> 
> Matteo
> 
> 
> 
> =========================================
> Fondazione Edmund Mach/CRI
> Department of Genomics and Biology of Fruit Crops
> Functional Genomics Team
> Via Mach 1
> 38010 San Michele all'Adige (TN)
> Italy
> Phone Office: ITA 0461615644
> =========================================
> 
> 
> 

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