Re: [galaxy-user] SAM to GFF ?

2011-02-18 Thread Hans-Rudolf Hotz

Hi Felix

It might be a little bit unusual to use the "generic feature format" 
(GFF) to show where your reads mapbut strictly speaking mapped reads 
on a genome are 'features' as well.


You can do it the following way:

first use the "Convert SAM to interval" tool (NGS: SAM Tools), and use 
the "BED-to-GFF converter" (Convert Formats)


I hope this helps, Hans



On 02/18/2011 01:22 PM, Peter wrote:

On Fri, Feb 18, 2011 at 12:08 PM, Felix Hammer  wrote:

Hi,
is there an easy way to use Galaxy to convert SAM to GFF?
thx,
Felix


How so?

SAM/BAM shows you where your reads map, GFF is used for
annotation (e.g. where the genes are and what they may do).

Are you talking about using SAM/BAM transcriptome mapping
(RNA-Seq) for gene finding?

Peter
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Re: [galaxy-user] SAM to GFF ?

2011-02-18 Thread vasu punj
I have used IGV with the Bam file and one ha sto generate index file which can 
be done in IGV, it work well. Gbrowser should also be OK. I think new version 
of IGV provide lot more features than previous one
Vasu.


--- On Fri, 2/18/11, Peter  wrote:


From: Peter 
Subject: Re: [galaxy-user] SAM to GFF ?
To: "Felix Hammer" 
Cc: galaxy-user@lists.bx.psu.edu
Date: Friday, February 18, 2011, 8:09 AM


On Fri, Feb 18, 2011 at 12:35 PM, Felix Hammer  wrote:
>
> Hi Peter,
> thx for the reply.
> You're right I want to display mapped RNA seq data in gBrowse.
> Currently I have the data in SAM format.
> Maybe I can figure out a trick using the text manipulation tools.
> thx,
> Felix

You forgot to CC the mailing list. If you want to use the data in
GBrowse then why not use SAM/BAM directly? I've not tried
it yet but I understand GBrowse can display BAM files... best
asking on their mailing list if you need more details. This
doesn't involve Galaxy directly though...

Peter
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  ___
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Re: [galaxy-user] SAM to GFF ?

2011-02-18 Thread Peter
On Fri, Feb 18, 2011 at 12:35 PM, Felix Hammer  wrote:
>
> Hi Peter,
> thx for the reply.
> You're right I want to display mapped RNA seq data in gBrowse.
> Currently I have the data in SAM format.
> Maybe I can figure out a trick using the text manipulation tools.
> thx,
> Felix

You forgot to CC the mailing list. If you want to use the data in
GBrowse then why not use SAM/BAM directly? I've not tried
it yet but I understand GBrowse can display BAM files... best
asking on their mailing list if you need more details. This
doesn't involve Galaxy directly though...

Peter
___
The Galaxy User list should be used for the discussion
of Galaxy analysis and other features on the public
server at usegalaxy.org. 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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Re: [galaxy-user] SAM to GFF ?

2011-02-18 Thread Peter
On Fri, Feb 18, 2011 at 12:08 PM, Felix Hammer  wrote:
> Hi,
> is there an easy way to use Galaxy to convert SAM to GFF?
> thx,
> Felix

How so?

SAM/BAM shows you where your reads map, GFF is used for
annotation (e.g. where the genes are and what they may do).

Are you talking about using SAM/BAM transcriptome mapping
(RNA-Seq) for gene finding?

Peter
___
The Galaxy User list should be used for the discussion
of Galaxy analysis and other features on the public
server at usegalaxy.org. 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:

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