Re: [galaxy-user] Samtools Mpileup output

2013-11-07 Thread Fabrice Besnard
Hi Carlos,

Thanks for your help: setting Genotype Likelihood Computation to
Perform genotype likelihood computation do give a bcf in output rather
that a pileup.
Then I use bcftools view to convert this bcf to a standard vcf format.

Fabrice

Le 06/11/2013 20:32, Carlos Borroto a écrit :
 On Wed, Nov 6, 2013 at 12:08 PM, Fabrice Besnard
 fbesn...@biologie.ens.fr wrote:
 
 Would you have any advice to select the output format, or alternatively,
 a tool in Galaxy that can convert pileup into .vcf?

 
 Hi Fabrice,
 
 I believe you only get the BCF output when Genotype Likelihood
 Computation is set to Perform genotype likelihood computation.
 
 Hope it helps,
 Carlos
 

-- 
Fabrice Besnard
Institute of Biology of the Ecole Normale Supérieure (IBENS)
46 rue d'Ulm, 75230 Paris cedex 05, France
8th floor. Office: Room 802. Lab: Room 817.
mail: fbesn...@biologie.ens.fr
Tel: +33-1-44-32-39-31
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[galaxy-user] Samtools Mpileup output

2013-11-06 Thread Fabrice Besnard
Hi,

I am using Mpileup from the Main Server (current version 0.0.1).
In theory, this tool can generate two formats of output files: either a
.bcf or a pileup.
However, I couldn't find the option to select a .bcf file, even when I
click on Set advanced options. When run, the program gives a pileup
output format.

Would you have any advice to select the output format, or alternatively,
a tool in Galaxy that can convert pileup into .vcf?

Many thanks for help,
-- 
Fabrice Besnard
Institute of Biology of the Ecole Normale Supérieure (IBENS)
46 rue d'Ulm, 75230 Paris cedex 05, France
8th floor. Office: Room 802. Lab: Room 817.
mail: fbesn...@biologie.ens.fr
Tel: +33-1-44-32-39-31
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Re: [galaxy-user] Samtools Mpileup output

2013-11-06 Thread Carlos Borroto
On Wed, Nov 6, 2013 at 12:08 PM, Fabrice Besnard
fbesn...@biologie.ens.fr wrote:

 Would you have any advice to select the output format, or alternatively,
 a tool in Galaxy that can convert pileup into .vcf?


Hi Fabrice,

I believe you only get the BCF output when Genotype Likelihood
Computation is set to Perform genotype likelihood computation.

Hope it helps,
Carlos
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