Using full path in the ini file fix the problem!
Thanks,
Yupu
On Jan 30, 2014, at 10:21, Jennifer Jackson j...@bx.psu.edu wrote:
Hi Yupu,
I'm sorry, I mixed up the processing for custom builds with the processing
for installed builds in my initial reply. A .2bit .len file are appropriate
Hi Yupu,
I'm sorry, I mixed up the processing for custom builds with the
processing for installed builds in my initial reply. A .2bit .len file
are appropriate for what you are doing - and the wiki instructions are
accurate.
Still, I double checked with Jeremy, the scientist that developed
Yupu,
Very glad! The thanks goes to Jeremy who sorted out the issue.
We had some big changes the last few release cycles, and unexpected
issues popped out. It was very nice of you to not only take the time to
report the problem, but to also follow up with sending feedback until
resolved.
Hi Yupu
Just double checking: Have you restarted your Galaxy server after adding
the len files?
Regards, Hans-Rudolf
On 01/28/2014 08:12 PM, Yupu Liang wrote:
Hi,
I am trying to set up the visualization functionality on our local Galaxy
installation. I followed the instructions on
Yes I have restarted my Galaxy many times and I have also tried different
genome build such as hg18 and experience the same problem.
Yupu
On Jan 29, 2014, at 3:32, Hans-Rudolf Hotz h...@fmi.ch wrote:
Hi Yupu
Just double checking: Have you restarted your Galaxy server after adding the
Hello Yupu,
Using a .len file is problematic at this time. In the upcoming release
this will be corrected. Using a .fasta file is the solution. In many
cases, using a .fasta file can be preferred as it will include the
reference genome sequence in the visualization, but the choice is yours,
Hi Jen,
I just tried it again. Just in case I cleared my browser, Firefox, cache,
history and cookies, although not memorized passwords. The saved
visualization gave me the Guru mediation error ,
GURU MEDITATION: #202b9e1bd2a8460a8089153f0853e7f4,
and when trying to visualize a bam file I
Hello Peggy,
The reference genome named simply arabidopsis in Galaxy is a legacy
genome name and may not work with all tools. Assigning the reference
genome name Arabidopsis_thaliana_TAIR9 instead is the recommended
choice (both are TAIR9).
The next item to change is the format of the
Oh btw I just looked at the list of loaded system-installed builds. there
are 934 genomes if I am not wrong.
browsing 5 by 5 is quite excruciating!
On 6 September 2011 21:00, Kevin Lam wrote:
I found the dropdown menu list to be too long to be effectively used
especially when viewed i chrome
=== Please use Reply All when responding to this email! ===
Hi Jen, I have been using the following link for learning to visualize TOPHAT
results:
http://main.g2.bx.psu.edu/u/jeremy/p/galaxy-rna-seq-analysis-exercise
How can get the RefGENE for the whole human genome instead of Ch19 listed in
I use IGV outside of Galaxy. If you download your bam and bam index
files you can load those and your reference into IGV to visualise them.
On 04/08/2011 00:03, Jiannong Xu wrote:
Hi Jen,
I mapped illumine reads to draft genomic contigs, and try to visualize the
mapping. Is there any way I
Jiannong,
Hans is on right track. You can indeed visualize your data using Trackster,
Galaxy's genome browser; Trackster is available via the Visualization tab.
Here are the steps needed to visualize your dataset:
(1) Use the [FASTA Manipulation -- Compute Sequence length] tool to compute
IGV should allow you to do this but not sure about trackbrowser in Galaxy.
Vasu
--- On Wed, 8/3/11, Jiannong Xu j...@nmsu.edu wrote:
From: Jiannong Xu j...@nmsu.edu
Subject: [galaxy-user] visualization
To: galaxy-user@lists.bx.psu.edu galaxy-user@lists.bx.psu.edu
Date: Wednesday, August 3,
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