Hello Jennifer
Thanks for your reply.  I am not familiar with SAMTools in UCSC Browser, so it 
is difficult for me to do the command line thing.
I tried to load the "Filter pileup" on to the UCSC Genome Browser within 
Galaxy, but it is not loading.  I also tried the tabular version of the "Filter 
pileup", with the same outcome.  Further, I tried to save the Filter pileup as 
a file and load it on the browser (outside Galaxy) but no luck.  Any 
suggestions?
Shashi

________________________________________
From: Jennifer Jackson [[email protected]]
Sent: Wednesday, June 02, 2010 2:46 PM
To: Shashikant Pujar
Cc: [email protected]
Subject: Re: [Genome] Custom Track Question

Hello Shashi,

You have some choices:

Using SAM Tools on the command line, samtools pileup -c will call
variants from the SAM/BAM alignments with BED output. This could be
loaded at a custom track. This may be the quickest method if your
dataset is very large.

Or, you can use Galaxy and load the results as a custom track. Send your
existing BAM custom track data from the Table browser (if not too large)
or upload files directly, then after the analysis, view results in the
UCSC browser. At Galaxy, see "NGS: SAM Tools -> Generate pileup & Filter
pileup".

Links from UCSC:
   http://genome.ucsc.edu/ -> Galaxy (left blue bar)
   from Table browser: Check "Galaxy" box in output section
Or directly: http://galaxy.psu.edu/

Hopefully this helps,
Jennifer

---------------------------------
Jennifer Jackson
UCSC Genome Informatics Group
http://genome.ucsc.edu/

On 6/2/10 7:03 AM, Shashikant Pujar wrote:
> Hi
>
> I have loaded a custom track (Illumina NGS reads in BAM format of a 2Mb 
> region) on the UCSC Dog Genome Browser.  Is there a way I can extract all 
> SNPs and Indels between the custom track and canFam2?
>
> Thanks
>
> Shashi Pujar
> _______________________________________________
> Genome maillist  -  [email protected]
> https://lists.soe.ucsc.edu/mailman/listinfo/genome

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