Hi Galaxy Users,
I am trying to understand the process of adding new entries to the genome 
builds dropdown list and also ensuring these new genome entries are 
appropriately mapped to a reference sequence.  I have been working through the 
code to work it out myself, but it would be helpful to get some advice from 
another user or possibly a developer who has experience with this process to 
avoid possible pitfalls.  It would be a nice future enhancement to expose this 
functionality to administrators.  Any advice would be appreciated! 
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