Hi everyone,<br><br>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.<br><br>From Encode download page, i got some files corresponding to peaks of these hsitone modifications and would like to know if there is a way to create a pipeline using galaxy to map my variants, depending on genomic 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 start using Galaxy ?<br><br>Thank you<br><br>Rad<br clear="all"><br><br>