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#1 |
Junior Member
Location: Melbourne, Australia Join Date: Feb 2010
Posts: 1
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I have a few total RNA samples that I would like to prepare for the Illumina GA platform, however they are just below the threshold stated in the protocol for processing for mRNA-seq. They recommend 1-10ug total RNA, but I have 800ng in my sample. Has anyone validated this protocol for lower amount of starting material (total RNA)? I would like to avoid pre-amplification of my RNA if possible. Cheers!
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