Hello
I am having a problem running Cuffdiff on some RNA-seq data. I want to
compare 2 of my conditions. I successfully used Cuffdiff three days ago to
compare two sets of data that are processed the exact same way (align with
Tophat and use Picard to confirm adequate alignment). I am using
Hello
I would like to visualize the tracks of my tophat accepted hits bam file.
I ran my first sample that was ~10,000,000 reads and it could be visualized
in both Trackster and the UCSC genome browser. When I tried to visualize
my other samples (which ranged from 15,000,000 to 35,000,000 reads)
January 20, 2012 Galaxy Development News Brief
Highlights:
* New Object Store data integration layer introduced
* RNA-seq updates: TopHat to 1.4.0 and Cufflinks, CuffDiff,
CuffCompare to 1.3.0.
* Tool Shed installation features and community tool additions
* Trackster performance upgrades and
Hi Greg,
We have a tutorial workflow from one of our publications that would be a
good test case to use:
http://usegalaxy.org/heteroplasmy
It contains complete references and the text walks through from start to
end and includes expected results.
The Shared Workflows area on Galaxy main
Hello Erin,
This was a temporary problem due to a new filesystem we installed during
this time frame, that has since been resolved. Please try again and if
the problem persists, please send a bug report from the error dataset
using the green bug icon. This allows us to gain access to the
Erin,
This was due to a temporary issue that has been fixed. However, you'll need to
copy the problematic datasets and use the new copy for visualization. To copy
datasets, use History Options -- Copy Datasets; you can select the source
history as your target history to copy datasets within a
Hello Tao,
This genome is labeled in Galaxy as:
Vibrio cholerae O1 biovar eltor str. N16961 (vibrChol1)
However, I am guessing that the genome is not indexed for the tools you
want to use it with. This means that you will need to use it as a custom
reference genome. The first step is to
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