Re: [galaxy-user] Variant annotation in galaxy

2014-02-25 Thread garzetti

Hi Jen,

thanks for your answer!

Unfortunatelly I cannot run Galaxy locally (in my Institute we only have 
Windows computers), but I can try on a cloud. I have a DIAG account, do 
you know if Galaxy works there?


Debora
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[galaxy-user] Variant annotation in galaxy

2014-02-24 Thread garzetti

Hallo Galaxy users,

I would like to annotate variants (in vcf file) found in my bacterial 
genomes and look which of them cause non-synonymous mutations. I have 
found two tools in the Main Galaxy that I can use for this purpose 
(snpEff and Annovar), but I have problems with them.


How can I change the input genome in snpEff? The only available choice 
in C. elegans. How can I choose my genome, already uploaded in my history?


Regarding Annovar, which file formats are required as Gene annotations/ 
Annotation Regions/ Annotation Databases? Reading the tool manual, it 
seems I can create my own txt/tabular files and use them for annotation, 
but  the tool in Galaxy doesn't allow me  to select any file, even if I 
have txt files in my history.


Any other suggested tool I can use?

Thanks!
Debora
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Re: [galaxy-user] Variant annotation in galaxy

2014-02-24 Thread Jennifer Jackson

Hello Debora,

There are no current plans to include additional genomes to the SnpEff 
tool on the public Main Galaxy instance at http://usegalaxy.org.


For the ANNOVAR tool, the supported genome at this time is hg19. When 
a .vcf file is assigned to that reference genome (aka database), the 
tool form fills out to display the available annotation to select from. 
This tool is a brand-new implementation and still undergoing 
development, so I cannot comment yet about future plans.


The best solution is to either run a local Galaxy (with sufficient 
resources) or what is probably more practical for many scientific end 
users, a cloud Galaxy or possibly a Slipstream Appliance. The tool 
wrappers for both tools are in the Tool Shed, so it can be installed and 
used within your Galaxy, where you can add in any genome that you want 
that has the appropriate reference data available. The reference data 
formats can be found on the originating tool sites with supplemental 
help notes in the Tool Shed repositories.


Help to get started is in these links:
https://wiki.galaxyproject.org/BigPicture/Choices
https://wiki.galaxyproject.org/Tool%20Shed

Hopefully one of these solutions will work out you. If there is more to 
share, we will send a followup reply,


Jen
Galaxy team

On 2/24/14 3:39 AM, garzetti wrote:

Hallo Galaxy users,

I would like to annotate variants (in vcf file) found in my bacterial 
genomes and look which of them cause non-synonymous mutations. I have 
found two tools in the Main Galaxy that I can use for this purpose 
(snpEff and Annovar), but I have problems with them.


How can I change the input genome in snpEff? The only available choice 
in C. elegans. How can I choose my genome, already uploaded in my 
history?


Regarding Annovar, which file formats are required as Gene 
annotations/ Annotation Regions/ Annotation Databases? Reading the 
tool manual, it seems I can create my own txt/tabular files and use 
them for annotation, but  the tool in Galaxy doesn't allow me to 
select any file, even if I have txt files in my history.


Any other suggested tool I can use?

Thanks!
Debora
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Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
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use the Galaxy Development list:

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--
Jennifer Hillman-Jackson
http://galaxyproject.org

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