Hi,

I don't unerstand because I have zlib and I have always the samer errors.

mpicxx  -lz -lbz2  code/TheRayGenomeAssembler.a RayPlatform/libRayPlatform.a
-o Ray
code/TheRayGenomeAssembler.a(FastqGzLoader.o): In function
`FastqGzLoader::open(std::basic_string<char, std::char_traits<char>,
std::allocator<char> >, int)':
FastqGzLoader.cpp:(.text+0x39): undefined reference to `gzopen'
FastqGzLoader.cpp:(.text+0x6f): undefined reference to `gzgets'
FastqGzLoader.cpp:(.text+0x8d): undefined reference to `gzclose'
FastqGzLoader.cpp:(.text+0x9a): undefined reference to `gzopen'
code/TheRayGenomeAssembler.a(FastqGzLoader.o): In function
`FastqGzLoader::load(int, ArrayOfReads*, MyAllocator*, int)':
FastqGzLoader.cpp:(.text+0x15e): undefined reference to `gzgets'
FastqGzLoader.cpp:(.text+0x1b4): undefined reference to `gzclose'
code/TheRayGenomeAssembler.a(BzReader.o): In function
`BzReader::readLine(char*, int)':
BzReader.cpp:(.text+0x82a): undefined reference to `BZ2_bzRead'
BzReader.cpp:(.text+0x8f5): undefined reference to `BZ2_bzReadOpen'
BzReader.cpp:(.text+0x9fa): undefined reference to `BZ2_bzReadGetUnused'
BzReader.cpp:(.text+0xa27): undefined reference to `BZ2_bzReadClose'
collect2: ld a retourné 1 code d'état d'exécution
make: *** [Ray] Erreur 1

Could you help me please?
Thank you.

Best regards
Frederic Texier.

-----Message d'origine-----
De : Sébastien Boisvert [mailto:[email protected]] 
Envoyé : mardi 12 février 2013 14:55
À : frederic texier
Cc : [email protected]
Objet : Re: Ray output



On 02/12/2013 05:15 AM, frederic texier wrote:
> Bonjour de nouveau,
>
> J'ai un problème quand je veux installer avec l'otpion HAVE_LIBZ=y.
> Faut-il un module supplémentaire à installer avant?
>

Yes, you need zlib headers.

On Debian or Ubuntu or other Debian-derived distributions:

sudo apt-get install -y zlib1g-dev


On Fedora or CentOS or other similar distribution:

sudo yum install -y zlib-devel


There is also the option HAVE_LIBBZ2=y that provides native support for
fastq.bz2 files.
  
> Je vous remercie.
> Cordialement
> Frédéric Texier.
>
> -----Message d'origine-----
> De : Sébastien Boisvert [mailto:[email protected]]
> Envoyé : vendredi 8 février 2013 18:05 À : frederic texier Cc : 
> [email protected]
> Objet : Re: Ray output
>
> Bonjour Frédéric,
>
> There is a work-in-progress to add this feature [1], although it's not 
> in the current backlog [2].
>
> Current available courses of action are:
>
> 1. use -amos option to generate a AMOS file with Ray and then parse 
> this to obtain the information you want (used reads, and so on).
>
> 2. Map your reads on contigs (or on scaffolds) with a aligner and then 
> pipe this in a existing tool (I am sure there exists tools for that 
> that take a SAM file as input).
>
>
> Also, if you want to visualize your assemblies to do some quality 
> controls (usually production departments like to do quality controls), 
> you can use Ray Cloud Browser.
>
>
> Demo: http://genome.ulaval.ca/corbeillab/Ray-Cloud-Browser/
> Source code:  https://github.com/sebhtml/Ray-Cloud-Browser
> Deployment instructions:
> https://raw.github.com/sebhtml/Ray-Cloud-Browser/master/Documentation/
> Deploy
> ment.txt
>
>
> ---
> [1] https://github.com/sebhtml/ray/issues/65
> [2] https://github.com/sebhtml/ray/issues?milestone=5&state=open
>
>
>
>
> Sébastien Boisvert
> Community Manager, Ray Genomics Software Suite PhD student, Université 
> Laval
>
> On 02/08/2013 09:05 AM, frederic texier wrote:
>> Hello,
>>
>> I have used Ray to assemble bacterial genome but I don't know where 
>> find
> the number of reads really used and the numer of reads not used in the 
> output.
>>
>> could you help me to find this, please?
>>
>> Thank you.
>> --
>>
>> Frédéric Texier
>>
>> Téléphone: +33(0)359317403
>> E-mail: [email protected]
>>
>> Genoscreen
>> Campus Pasteur - 1 rue du Pr Calmette
>> 59000 Lille
>> Téléphone: +33(0)320877153
>>
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