On 05/12/11 12:37 AM, Zhengshuang Hua wrote:
> Hi,
> I'm doing assembly of a metagenome of a non reference organism. Our 
> dataset is about 250G. I'm so glad to find the software Ray which can 
> assemble in parallel. The version which I used is Ray_1.7. I run it on 
> a cluster with 18 nodes(216 cores in total) But when I execute the Ray 
> program. I find there is no output named contig.fasta when the job 
> finished. The command is :
> mpirun -np 216 /parastor/users/shuws/software/ray_1.7/Ray -k 79 -p 
> /parastor/users/shuws/data/soil_metagenome/1107KHS-0021/Soil_DNA_1.fastq 
> /parastor/users/shuws/data/soil_metagenome/1107KHS-0021/Soil_DNA_2.fastq 
> -write-contig-paths -write-seeds -write-extensions -o Ray_assemble_v1_7_2
>

What is the peak coverage in CoverageDistributionAnalysis.txt ?

The standard output presumably contains something like 'Assembly panic: 
no peak coverage observed,
please lower the k-mer length'.

We are presently working on méta-Ray -- modifications to enable Ray on 
massive metagenomics
datasets.

> All files i get is listed below:
>     CoverageDistributionAnalysis.txt
>     CoverageDistribution.txt
>     MessagePassingInterf
>     MessagePassingInterface.txt
>     MessagePassingInterfP
>     NetworkTest.txt
>     NumberOfSequences.txt
>     RayCommand.txt
>     RayVersion.txt
>     SequencePartition.txt



> I don't know why it has such problem.

See above.

> I saw the standard error file with nothing in it. Also, standard 
> output file have no useful information about the job which I run. 
> Without any error information, I don't know what to do. So, can you 
> help me about the question or give me some advice?

Try to lower the k-mer length (let's say 31).

>         Thanks very much!
>


>
>                                                                    Hua 
> Zhengshuang


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