Hi Zach,
Would you have time to send this in as a bug report so that we can take
a closer look? Format problems are likely the issue, but this can be
double checked. To report as a bug, click on the green bug icon in the
error dataset's box in your history. If your Galaxy account uses a
Hi Zach,
You should reply to all so people dont keep working on your questions. Glad
to help.
Austin
-- Forwarded message --
From: Zachary A Lewis zle...@uga.edu
Date: Tue, Sep 13, 2011 at 3:10 PM
Subject: Re: [galaxy-user] Help with sam to bam
To: Austin Paul austi...@usc.edu
Thanks Austin, good suggestions all around. The question came through
again, so I didn't realize this was completely solved. Glad this was
just a format issue!
Take care,
Jen
Galaxy team
On 9/14/11 4:54 PM, Austin Paul wrote:
Hi Zach,
You should reply to all so people dont keep working on
Hi Diana,
As Anton mentioned, we can add this genome to our working list. A
check-in with UCSC about their plans for an update seems appropriate and
that will be part of our prioritization of this genome.
Meanwhile, the fastest way for you to start working with this genome
right away is to
I have 3 illumina paired end reads of exome capture of the sample. I want
to assemble these reads to genome using tools available in Galaxy (BWA etc).
My concern is the amount of data that I can analyzed and when these reads
should be merged. The total size of data is +30Gb.
Thanks,
Arun
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