1. Using a k-mer length of 71 will _presumably_ not work very well
because of sequencing errors. First do a test run at k=31.


2. Are your interleaved files properly generated ?

sequence1/1
sequence1/2
sequence2/1
sequence2/2
sequence3/1
sequence3/2


Do you get anything in LibraryStatistics.txt ?

On Thu, 2012-03-01 at 17:06 -0500, LIU wrote:
> Hi There,
> 
> I have been using Ray to de novo assembly.
> 
> The input reads are a mix of illumina pair-end reads (this account for
> 90%), illumina single-end reads and 454 single end reads. 
> 
> The command i used is 
> mpiexec -n 60 Ray \
>  -i \
>  /home/s4196896/mix_assembly/input/t15c15/gs1.shuffled.fasta.gz \
>  -i \
>  /home/s4196896/mix_assembly/input/t15c15/gs2.shuffled.fasta.gz \
>  -i \
>  /home/s4196896/mix_assembly/input/t15c15/gs3.shuffled.fasta.gz \
>  -s \
>  /home/s4196896/mix_assembly/input/t15c15/gs2.single.fasta.gz \
>  -s \
>  /home/s4196896/mix_assembly/input/t15c15/gs3.single.fasta.gz \
>  -s \
>  /home/s4196896/mix_assembly/input/t15c15/gs1.single.fasta.gz \
>  -s \
>  /home/s4196896/mix_assembly/input/radseq1.seeds.fasta \
>  -s \
>  /home/s4196896/mix_assembly/input/radseq_v2.fasta \
>  -s \
>  /work1/s4196896/454_assembly/raw_reads/all_genomic_reads.short.fasta
> \
>  -s \
>  /work1/s4196896/454_assembly/raw_reads/all_genomic_reads.long.fasta \
>  -o \
>  71 \
>  -k \
>  71
> 
> The output shows that scaffolds and contigs are the same (same N50,
> total number of bases and number of sequences etc.).
> 
> This confused me.
> 
> 
> I hope someone can help me out.
> 
> Thanks in advance.
> 
> Kind Regards,
> -- 
> Huanle 
> 
> School of biological Sciences, UQ, QLD, AU



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