I had the same problem with ubuntu 12.04 and 12.10 and the stable Ray release. 
I was able to successfully compile the program and be able to use .gz files 
after following the instructions in this mailing list entry

http://lists.debian.org/debian-med/2012/11/msg00015.html


But this version works - ie. simply putting the $LD_FLAGS after the input files 
on line 189 of the Makefile:

tbooth@balisaur[ray_2.1.0]mpicxx -Wl,-Bsymbolic-functions -Wl,-z,relro 
code/TheRayGenomeAssembler.a RayPlatform/libRayPlatform.a -lz -lbz2 -o Ray

Anthony

On 13/02/2013, at 5:14 AM, Sébastien Boisvert wrote:

What GNU/Linux distribution are you using ?

On 02/12/2013 11:21 AM, frederic texier wrote:
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.




[cid:[email protected]]


Anthony Borneman
Principal Research Scientist - Molecular Biology  | The Australian Wine 
Research Institute
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-----Message d'origine-----
De : Sébastien Boisvert [mailto:[email protected]]
Envoyé : mardi 12 février 2013 14:55
À : frederic texier
Cc : 
[email protected]<mailto:[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]<mailto:[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]<mailto:[email protected]>

Genoscreen
Campus Pasteur - 1 rue du Pr Calmette
59000 Lille
Téléphone: +33(0)320877153

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