Is there any tool/ combination of tools with in galaxy which can detect CNV. I have 100X paired sequencing data between cancer and normal.
Thanks
Hello,
The tool "FreeBayes" may be of interest. Please see the tool form for links to the primary tool documentation to see if the functionality will meet your needs.
Best,
Jen Galaxy team
On 8/15/12 4:46 AM, shamsher jagat wrote:
Is there any tool/ combination of tools with in galaxy which can detect CNV. I have 100X paired sequencing data between cancer and normal. Thanks
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:
Thanks Jen, I am also intrested in this. Has any one used FreeBayes in Galaxy or out side Gaaxy to detect CNV from a ilumina sequencing data. Is their a tutorial for running this tools. Thanks.
From: Jennifer Jackson jen@bx.psu.edu To: shamsher jagat kanwarjag@gmail.com Cc: galaxy-user@lists.bx.psu.edu Sent: Thursday, August 16, 2012 12:48 AM Subject: Re: [galaxy-user] copy number variation detcetion in Glaxay
Hello,
The tool "FreeBayes" may be of interest. Please see the tool form for links to the primary tool documentation to see if the functionality will meet your needs.
Best,
Jen Galaxy team
On 8/15/12 4:46 AM, shamsher jagat wrote:
Is there any tool/ combination of tools with in galaxy which can detect CNV. I have 100X paired sequencing data between cancer and normal. Thanks
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:
Hi Mathew,
To clarify, freebayes is not designed to detect CNVs. It can CNV information detected in another method to correctly genotype at sites with copy number variations.
If you have exome data, there is conifer http://http://conifer.sourceforge.net/ conifer.sourceforge.net/ http://conifer.sourceforge.net/.
For more general applications, there is ERDS, http://www.duke.edu/~mz34/erds.htm
I don't know if either of these will suit your needs. I use the CNV input methods in freebayes regularly for known, large variations in copy number, such as are seen on mammalian sex chromosomes.
Best, Erik On Aug 16, 2012 11:11 AM, "Mathew Bunj" mathewbunj@yahoo.com wrote:
Thanks Jen,
I am also intrested in this. Has any one used FreeBayes in Galaxy or out side Gaaxy to detect CNV from a ilumina sequencing data. Is their a tutorial for running this tools.
Thanks.
*From:* Jennifer Jackson jen@bx.psu.edu *To:* shamsher jagat kanwarjag@gmail.com *Cc:* galaxy-user@lists.bx.psu.edu *Sent:* Thursday, August 16, 2012 12:48 AM *Subject:* Re: [galaxy-user] copy number variation detcetion in Glaxay
Hello,
The tool "FreeBayes" may be of interest. Please see the tool form for links to the primary tool documentation to see if the functionality will meet your needs.
Best,
Jen Galaxy team
On 8/15/12 4:46 AM, shamsher jagat wrote:
Is there any tool/ combination of tools with in galaxy which can detect CNV. I have 100X paired sequencing data between cancer and normal. Thanks
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:
-- Jennifer Jackson 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
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
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:
Thanks Erik, I was also not very clear about Freebayes use in CNV detection. Thanks for clarifiaction. Mathew
From: Erik Garrison erik.garrison@bc.edu To: Mathew Bunj mathewbunj@yahoo.com Cc: shamsher jagat kanwarjag@gmail.com; Jennifer Jackson jen@bx.psu.edu; "galaxy-user@lists.bx.psu.edu" galaxy-user@lists.bx.psu.edu Sent: Thursday, August 16, 2012 3:12 PM Subject: Re: [galaxy-user] copy number variation detcetion in Glaxay
Hi Mathew, To clarify, freebayes is not designed to detect CNVs. It can CNV information detected in another method to correctly genotype at sites with copy number variations. If you have exome data, there is conifer http://conifer.sourceforge.net/conifer.sourceforge.net/. For more general applications, there is ERDS, http://www.duke.edu/~mz34/erds.htm I don't know if either of these will suit your needs. I use the CNV input methods in freebayes regularly for known, large variations in copy number, such as are seen on mammalian sex chromosomes. Best, Erik On Aug 16, 2012 11:11 AM, "Mathew Bunj" mathewbunj@yahoo.com wrote:
Thanks Jen,
I am also intrested in this. Has any one used FreeBayes in Galaxy or out side Gaaxy to detect CNV from a ilumina sequencing data. Is their a tutorial for running this tools. Thanks.
From: Jennifer Jackson jen@bx.psu.edu To: shamsher jagat kanwarjag@gmail.com Cc: galaxy-user@lists.bx.psu.edu Sent: Thursday, August 16, 2012 12:48 AM Subject: Re: [galaxy-user] copy number variation detcetion in Glaxay
Hello,
The tool "FreeBayes" may be of interest. Please see the tool form for links to the primary tool documentation to see if the functionality will meet your needs.
Best,
Jen Galaxy team
On 8/15/12 4:46 AM, shamsher jagat wrote:
Is there any tool/ combination of tools with in galaxy which can detect CNV. I have 100X paired sequencing data between cancer and normal. Thanks
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:
-- Jennifer Jackson 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
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
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:
galaxy-user@lists.galaxyproject.org