Dear Sebastien,

thanks a lot, that was really helpful! Our first testassemblies with ray 
are very promising!

best regards
Andrea Thürmer


On 26.7.13 16:55, Sébastien Boisvert wrote:
> [Please use the mailing list, to subscribe: 
> http://lists.sourceforge.net/lists/listinfo/denovoassembler-users ]
>
>
> Hi Andrea,
>
> On 26/07/13 10:05 AM, JACQUES CORBEIL wrote:
>>
>> Begin forwarded message:
>>
>>> *From: *Andrea Thuermer <athu...@gwdg.de <mailto:athu...@gwdg.de>>
>>> *Subject: **Ray meta*
>>> *Date: *26 July, 2013 10:02:09 AM EDT
>>> *To: *<jacques.corb...@crchul.ulaval.ca 
>>> <mailto:jacques.corb...@crchul.ulaval.ca>>
>>>
>>> Dear Jacques and other co-authors of Ray meta,
>>>
>>> we are a sequencing center and some of our main scientific interests 
>>> are microbial genomics, metagenomics and (meta)transcriptomics. That 
>>> s why we are always interested in new assemblers.
>>> I was happy when i found your Ray Meta assembler.
>
> I am also happy that you found it.
>
>>> I am currently testing the it. Do you have any experience with long 
>>> reads with your assembler?
>>> With -long- i think about reads
>>> between 2 - 10 kb, concerning the new moleculo method that illumina 
>>> has announced?!
>
> I have not tried Moleculo reads with Ray, but I checked some reads and 
> they very few errors like Illumina reads.
>
> I you want to test, there are these two fastq files (you just need to 
> register on BaseSpace):
>
> https://basespace.illumina.com/sample/2354355/files/raw/mol-32-2832.fastq.gz?id=142199664
>  
>
>
> https://basespace.illumina.com/sample/2346352/files/raw/mol-32-281c.fastq.gz?id=142202448
>  
>
>
>
> There is also this paper 
> http://elife.elifesciences.org/content/2/e00569/article-data with 
> Moleculo data,
> but strangely the data was not released even though the paper is 
> published !
> Moleculo data for this paper should hopefully appear soo at the 
> address http://genepyramid.stanford.edu/botryllusgenome/download/
>
>
>>> Are there any experience maybe with pacBio data so far?
>
> Ray does not perform any error correction.
>
> If you use Pacific Biosciences circular consensus data, Ray will work. 
> But for long Pacific Biosciences SMRT uncorrected data,
> that won't work.
>
>>> Another problem, i could not found in the manual, does the software 
>>> have problems with the sff-files that are generated after a 454 run 
>>> with flow pattern B?
>
> Ray has native support for sff files. However, paired reads in sff 
> files are not extracted as pairs.
>
> I don't know what is a "pattern B" so I can answer that question I am 
> afraid.
>
>>> I have no results
>>> so far, but the software did not like these sff-files as input, 
>>> "old" sff-files before the software upgrade seem to be no problem.
>
> The implementation if based on this specification:
>
>  * \see Section "13.3.8 Standard Flowgram Files (.sff)"
>  * Genome Sequencer, Data Analysis Software Manual, Software Version 
> 2.0.00, October 2008, page 528
>  * http://sequence.otago.ac.nz/download/GS_FLX_Software_Manual.pdf
>
>>>
>>> Thanks in advance!
>>>
>>> Best reards
>>> Andrea
>>>
>>> -- 
>>> Dr. Andrea Thürmer
>>> - Sequencing -
>>>
>>> Universität Göttingen
>>> Labor für Genomanalyse
>>> Grisebachstraße 08
>>> 37077 Göttingen
>>>
>>> email: athu...@gwdg.de <mailto:athu...@gwdg.de>
>>> Tel.: 0551/39-33841
>>>
>>>
>>>
>>
>


-- 
Dr. Andrea Thürmer
- Sequencing -

Universität Göttingen
Labor für Genomanalyse
Grisebachstraße 08
37077 Göttingen

email: athu...@gwdg.de
Tel.: 0551/39-33841




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