Please keep me on the loop as I am also interested in similar workflow.<br>Many thanks and best regards,<br>Jorge<br><br><div class="gmail_quote">On Thu, Jun 23, 2011 at 3:21 AM, Jennifer Jackson <span dir="ltr">&lt;<a href="mailto:jen@bx.psu.edu">jen@bx.psu.edu</a>&gt;</span> wrote:<br>
<blockquote class="gmail_quote" style="margin: 0pt 0pt 0pt 0.8ex; border-left: 1px solid rgb(204, 204, 204); padding-left: 1ex;">Hello Rad,<br>
<br>
Dan will be able to help you get started and build up a workflow for your analysis. He is currently on vacation, but will be returning soon and will contact you directly when he returns.<br>
<br>
We are very sorry about the delayed reply. Please know that we definitely want to help you to use Galaxy for your project,<br>
<br>
We will be in touch,<br>
<br>
Best,<br>
<br>
Jen<br>
Galaxy team<div><div></div><div class="h5"><br>
<br>
<br>
On 6/17/11 10:55 AM, Radhouane Aniba wrote:<br>
</div></div><blockquote class="gmail_quote" style="margin: 0pt 0pt 0pt 0.8ex; border-left: 1px solid rgb(204, 204, 204); padding-left: 1ex;"><div><div></div><div class="h5">
Hi everyone,<br>
<br>
I have a list of genomic regions with some variants and would like to<br>
study the correlation between theses variants and epigenomics marks such<br>
as histone modifications.<br>
<br>
 From Encode download page, i got some files corresponding to peaks of<br>
these hsitone modifications and would like to know if there is a way to<br>
create a pipeline using galaxy to map my variants, depending on genomic<br>
regions to the information I have from the histone modification peaks.<br>
<br>
Is there someone who can point me to a step by step to do things to<br>
start using Galaxy ?<br>
<br>
Thank you<br>
<br>
Rad<br>
<br>
<br>
<br>
<br></div></div>
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