Re: [galaxy-user] promoter question

2011-07-25 Thread Jennifer Jackson

Hello Rami,

The tool "Operate on Genomic Intervals -> Get flanks" will return 
reference genomic sequence upstream/downstream from a set of 
coordinates, which is essentially what the UCSC Genome Browser is doing 
when you use the export promoters option. This tool requires that you 
already have a set of genomic intervals (a data track) from an 
annotation data source. UCSC is only one choice. Please see all directly 
linked data sources listed under "Get Data". Or, locate your own and 
load via URL (http/ftp) or a file that you have already downloaded to 
your computer/server (use ftp if large).


Please note that this tool will function with most (but not all) genomes 
already part of the native reference genome set in Galaxy and must be 
assigned. To assign, use the "Edit Attributes" form by clicking on the 
pencil icon for the dataset.


Best!

Jen


On 7/25/11 11:55 AM, Rami Al-Ouran wrote:

Thank you very much for the quick response.

Does that mean there is no direct method in Galaxy (without using UCSC)
to get promoters from a list of gene symbols ?

Thank you,
Rami

On 7/25/2011 2:51 PM, Jennifer Jackson wrote:

Hello Rami,

The UCSC genome browser will result in one promoter sequence per
transcript, as many genes will have many associated transcripts.

Depending on which track you are obtaining data from, a "representative"
transcript for each gene may or may not be notated. If using "UCSC
Genes", the tables associated with the primary table knownGenes to
examine are knownIsoforms and knownCanonical, which will show how
transcripts are clustered. You can link these tables together using the
output option "selected fields from primary and related tables".

Alternatively, you may already have already selected a set of
transcripts (not genes) to obtain data from. In that case, enter the
identifiers directly into the UCSC Table browser's "identifiers" field
when performing the query (paste or upload text file). Or pull all into
Galaxy and join with your identifier list to subset the results.
Identifiers must be in the same format as used by the track of interest
for this method to work.

If you are having trouble with the Table browser, the UCSC Genome team
can help through their mailing list at http://genome.ucsc.edu

Hopefully this helps to explain the data,

Best,

Jen
Galaxy team

On 7/25/11 10:25 AM, Rami Al-Ouran wrote:

Hello,

Is there a way in galaxy to retrieve the promoter sequences for a list
of genes. I tried using UCSC genome browser, but in many cases it keeps
giving more than one promoter sequence per gene.

Thank you,
Rami
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--
Jennifer Jackson
http://usegalaxy.org/
http://galaxyproject.org/
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using "reply all" in your mail client.  For discussion of
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Re: [galaxy-user] promoter question

2011-07-25 Thread Jennifer Jackson

Hello Rami,

The UCSC genome browser will result in one promoter sequence per 
transcript, as many genes will have many associated transcripts.


Depending on which track you are obtaining data from, a "representative" 
transcript for each gene may or may not be notated. If using "UCSC 
Genes", the tables associated with the primary table knownGenes to 
examine are knownIsoforms and knownCanonical, which will show how 
transcripts are clustered. You can link these tables together using the 
output option "selected fields from primary and related tables".


Alternatively, you may already have already selected a set of 
transcripts (not genes) to obtain data from. In that case, enter the 
identifiers directly into the UCSC Table browser's "identifiers" field 
when performing the query (paste or upload text file). Or pull all into 
Galaxy and join with your identifier list to subset the results. 
Identifiers must be in the same format as used by the track of interest 
for this method to work.


If you are having trouble with the Table browser, the UCSC Genome team 
can help through their mailing list at http://genome.ucsc.edu


Hopefully this helps to explain the data,

Best,

Jen
Galaxy team

On 7/25/11 10:25 AM, Rami Al-Ouran wrote:

Hello,

Is there a way in galaxy to retrieve the promoter sequences for a list
of genes. I tried using UCSC genome browser, but in many cases it keeps
giving more than one promoter sequence per gene.

Thank you,
Rami
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org. Please keep all replies on the list by
using "reply all" in your mail client. For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

http://lists.bx.psu.edu/


--
Jennifer Jackson
http://usegalaxy.org/
http://galaxyproject.org/
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using "reply all" in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

 http://lists.bx.psu.edu/listinfo/galaxy-dev

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[galaxy-user] promoter question

2011-07-25 Thread Rami Al-Ouran

Hello,

Is there a way in galaxy to retrieve the promoter sequences for a list 
of genes. I tried using UCSC genome browser, but in many cases it keeps 
giving more than one promoter sequence per gene.


Thank you,
Rami
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using "reply all" in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:

 http://lists.bx.psu.edu/listinfo/galaxy-dev

To manage your subscriptions to this and other Galaxy lists,
please use the interface at:

 http://lists.bx.psu.edu/