David K Crossman wrote:
> Hello!
>
> We uploaded 12 samples to Galaxy last night via FTP. This
> morning, I went to "Get Data" and clicked on all 12 that were under the FTP
> location, chose the type of file they were and reference genome and then
> clicked "Excecute." The 12
Hello!
We uploaded 12 samples to Galaxy last night via FTP. This
morning, I went to "Get Data" and clicked on all 12 that were under the FTP
location, chose the type of file they were and reference genome and then
clicked "Excecute." The 12 moved over to the History panel and
Hi everyone,
I have a list of genomic regions with some variants and would like to study
the correlation between theses variants and epigenomics marks such as
histone modifications.
>From Encode download page, i got some files corresponding to peaks of these
hsitone modifications and would like t
Hello all,
There will be two Galaxy workshops at the University of Southern California
(USC) next week. Both are presented by Jeremy Goecks of Emory University and
the Galaxy team. *Both workshops are open to the public:*
*Galaxy: A web‐based workbench for interactive and reproducible analysis of
Hi,
I was trying to extract FASTA sequences using the following tab separated data
for Chicken on the Galaxy Main server:
chr5 4725816847259240
chr181938527 1939965
chr2 101973625 101974007
chr4 7565389875674045
chr194258837 4263299
chr4
Gaurav
> 1. Is there any help file explaining directory structure and what
all
> configuration files used for?
The Galaxy wiki is the best place to go for these things, as
Louise-Amelie said. You should be able to ignore most things in the
config files initially as they will "just work". You
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