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Old 10-12-2011, 06:00 AM   #1
Location: cambridge

Join Date: Apr 2010
Posts: 68
Default truseq exome enrichment

Sorry if this question has already been posted.

Has anyone tried to get around truseq's gel size selection when preparing libraries for exome enrichment?

We would normally use a 6 minute fragmentation as quoted by agilent but this gives post exome enrichment libraries of around 300bp or slightly over. Truseq want libraries to be 100bp larger.
We are trying to automate and remove gel size selection if possible.
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