Hi,
I have a table and would like to remove duplicate lines based on values in
the first column. Is there a simple way to do it in Galaxy?
Thanks,
Sebastien
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and o
Hi,
I have ChIP-seq alignment files in .bowtie format and would like to perform
peak-calling using MACS. However, .bowtie format doesn't seem to be
supported in Galaxy. Is there a way around to have MACS analyze these files
within Galaxy, or is the only option to use MACS in command line?
Thank y
Hi,
I am wondering if it is possible to convert from bigWig to wig format in
Galaxy.
Sincerely,
Sébastien Vigneau
___
The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at
Hi,
I can't import workflows from file on a freshly installed instance of
Galaxy on Amazon Cloud. The error message is copied below. Do you have some
idea on how to fix this?
Thanks,
Sébastien
Internal Server Error
> Galaxy was unable to sucessfully complete your request
> URL:
> http://ec2-50
Hi,
I have written a simple xml wrapper to run the UCSC *bigWigToBedGraph* tool
on a custom Galaxy install on Amazon cloud. The tool works as expected in
this install. The xml file itself is in
/mnt/galaxy/galaxy-app/tools/myTools, but I added the bigWigToBedGraph
binary to the /mnt/galaxy/tools/b
Hi 7plusorminus 3,
One possibility is to use the "group" tool with "max" operation, to get the
highest expressed exon for each gene. Then, you may use "subtract datasets"
to remove the highest expressed exons from the original dataset, and
iterate to get the second highest expressed exons (which a
6 matches
Mail list logo