Thanks Alban for your answer,
Our admin system has tested to run ChIPMunk externally but didn't
received the same error message.
In fact, pretty.rb lib is found.
It seems to be a difference between chiphorde version : we have
run_chiphorde4.rb instead of run_chiphorde.rb
Do you think that
Thanks to Marie-Stephane to have found that this error is due to a
diifference of verion.
Alban, could you please tell us which version (2 or 3) do you use in
your Galaxy tools, in order to install this version on our cluster ?
Thanks in advance,
Sarah
Sarah Maman a écrit :
Thanks Alban for
Is there any way of downloading processed files at galaxyproject.org by e.g.
FTP, instead of “Save as” in the web browser? I have some large (~50Gb) BAM
files to download, and downloading it via the browser is not stable.
Thanks, Karen.
Hello,
Can you share with me (a) the fasta dataset and (b) the form values (e.g. name,
dbkey, etc) you used when you encountered this error?
Thanks,
J.
On Jan 7, 2013, at 10:17 AM, Jennifer Hillman-Jackson wrote:
Repost to Galaxy-user
---
When using Trackster on Galaxy(
Hi Sarah,
It seems that Chipmunk is not well executed (reason why it can't found the log
file).
I think that there's some ruby libraries missing.
Please try to run ChIPMunk externally this way:
ruby /path/to/ChIPMunk/run_chiphorde.rb
If you receive this kind of error message, it means that
Hi,
You have to use ChIPMunk v2 with Nebula (I don't think its compatible with the
v3)
++,
Alban
--
Alban Lermine
Unité 900: INSERM - Mines ParisTech - Institut Curie
Bioinformatics and Computational Systems Biology of Cancer
11-13 rue Pierre et Marie Curie (1er étage) - 75005 Paris - France
Hi,
Another approach you can try is to use DESeq or EdgeR from Bioconductor to
assess differential expression.
I personally like these two methods LOTS better than Cuff* mainly because
they are a lot closer to tried and true statistical methods developed for
microarrays. I esp. like how both
Hello Karen,
From a shell/unix/terminal window on your side, use curl to download
datasets.
The link can be obtained by right clicking the floppy disk icon inside a
history item and choosing Copy Link Address (for most datasets) or
Download Dataset/Download bam_index (for BAM datasets
Hi community,
Due to the increasing Galaxy public servers
PublicGalaxyServershttp://wiki.galaxyproject.org/PublicGalaxyServers
it
would be very useful to have a search tool in order to look for software
ready-to-use in the public servers.
Since I know this is not available. Will it be feasible?
Not the most convenient solution, but what I normally do in this situation
is to combine the two files, filter then split again. There are tools for
combining and splitting paired fastq files in Galaxy.
Hope it helps,
Carlos
On Jan 8, 2013 12:55 AM, 柴田 弘紀 hshib...@gen.kyushu-u.ac.jp wrote:
Hi
Sorry to send you again and look forward any input abut joining
two overlapping reads Fastq files
Thanks
Kanwar
-- Forwarded message --
From: shamsher jagaut kanwar...@gmail.com
Date: Sun, Jan 6, 2013 at 2:24 PM
Subject: joining two FASTq files with overlap reads
To: galaxy-user
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