Hi,
I uploaded some file that resulted to be too big and my history showed that
that was not more space available. Now I deleted few file, and I should have
80 GB available, but my history shows still that I have no more space available
for analysis. Can anyone from the Galaxy team check this f
Hy guys,
I am performing some RNA sequencing. I am using a gtf file as a reference
annotation for the cufflink - cuffmerge steps. Then when I do the cuffdiff I
find something strange. Where there is the gene name, the corresponding values
(all of them!) are 0, where there is no gene name there a
Hi,
I have worked so far on the free web-based version of Galaxy; now I have
installed Bio-Linux 7, and there is Galaxy in there as well. However, I cannot
access to my data (stored on the web version of Galaxy) using Galaxy on Bio
Linux. If it is possible, does anyone know how to do it?
Thanks,
Hi,
is anybody else experiencing problems with the public Main Galaxy server at
http://main.g2.bx.psu.edu? It just does not work anymore.
Any suggestion?
Giuseppe Ianiri
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The Galaxy User list should be used for the discussion of
Galaxy a
Hi,
I want to compare gene deferentially expressed in two conditions (1 and 2). I
don't have a GTF reference annotation.
In my first attempt, I mapped my Illumina reads with TopHat. Then I run
Cufflink, and Cuffmerge on my Cufflink outputs for the conditions 1 and 2. At
the end, I run Cuffdiff u
Hello,
I performed my mapping using tophat - cufflink - cuffmerge - cuffdiff.
With the information I have for my analysis so far, I can reannotate wrong
genes, check for correct splicing etc. However, I would like to perform
some analysis post-alignment, like for example samples clustering, volcano
Hi all,
I got my cuffdiff output and I have to compare results from two (or eventually
more) different dataset.
Does anybody know if there is a way to do that on Galaxy?
Also more in general, is there a manual for the Galaxy tools? That would be
very helpful for someone who is new on the field (l
Hello guys,
I went through the RNAseq workflow (I didn't do Cuffmerge) and from the
Cuffdiff output gene and transcript differential expression testing I filtered
some data. For example, for two samples I got about 400 gene and 900 transcript
differential expressed with fold change >2. Since I a
From: Jennifer Jackson [j...@bx.psu.edu]
Sent: Thursday, November 29, 2012 10:51 AM
To: Ianiri, Giuseppe
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] filter for +/- 2-fold difference in expression levels
Hello Giuseppe,
Fold is included in the Cuffdiff output. Section
Hey guys,
I have my Cuffdiff output and I was trying to figure out how to get the data I
need.
I am interested in the outputs Transcript and Gene differential expressed. Does
anyone know how to filter for +/- 2-fold difference in expression levels?
Thank you
Giuseppe Ianiri, Ph.D.
Division of C
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