Hi,
I just read through the post at the following
link, http://lists.bx.psu.edu/pipermail/galaxy-user/2011-February/001934.html
I'm facing the same problem as well.
I'm desired to extract out the assembled transcript by Cufflink.
Can I know that how I link my output file from Tophat and Cufflink
Edge,
Please send questions like this to the galaxy-user mailing list, where many
people see your email and can help you and/or benefit from it. I've cc'd the
list for this reply.
The thread you linked to is out of date. To get sequences for the features in a
GTF file, you can use the 'Extract
Hi Vasu,
Would you be able to share a history link? You can email to me directly
and I can share with team if needed.
Thanks!
Jen
Galaxy team
On 5/9/11 7:58 PM, vasu punj wrote:
I am trying to use stat function of Galaxy, and compute q value from p
values. it is giving following errors:
An
Hello Oliver,
You can compare SNP datasets using the tools under "RGENETICS" and
"Human Genome Variation". dbSNP and 1000 Genomes data are locally cashed
in our Libraries, making them easy to load into a history and use.
Also, here is an example workflow that includes sample SNP analysis
(db
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