Hello,

On 04/04/13 04:57 PM, Hung-Ying Lin wrote:
>     Dear Dr. Boisvert,

I am not a doctor.

>
>     Please allow me to introduce myself. I'm Hung-Ying, currently a PhD 
> student in Genetics program at Iowa State University and I am conducting a 
> project that compares
>   performances among several assemblers using simulated illumina datasets.
>

By performance, do you mean assembly quality and things like that or you mean 
speed, scalability and memory usage. Or do you
mean ease of use ?

>     The project was almost completed. But to make sure I've tried  sufficient 
> numbers of parameter combinations and reach its optimum, I would like to have 
> some
>comments directly from the authors.

That's a good idea.

> The attachment is the result I have so far.

There is no attachment.

> Would you be willing to take a look and give me some suggestions.
>

Sure,

>
>     An additional question about the algorithm or mechanism behind hybrid 
> assembly in Ray. I have searched your papers, it mentioned Ray can support 
> hybrid assembly,
>  however I don't find any command in user manual.

Ray can use various sequencing technologies because it builds the de Bruijn 
graph using all k-mers from every sequence. Also,
various heuristics are used to browse the graph: paired reads, mate pairs, read 
threading, tip detection, and so on.

> Does it mean Ray can detect the length automatically?

Ray detects automatically (i.e. auto-calibration of paired read outer distance 
distributions).

>  How can I deal with hybrid assembly(illumina + 454 and illumina +
>contigs sequence) in Ray?

Just provide every file you have either as single-end reads (with -s 
file.fastq) or as
paired-end reads (with -p file1.fastq file2.fastq).

>
>
> Thank you in advance for your replying, your commons will be very important 
> to me and have a nice day.



>
>     Sincerely,
>     Hung-Ying
>


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