Has anyone tried Denaturing with NaOH and then followed by a heat denaturing?
In other words do both?
Does that help make better clusters??
Running a MiSeq
In other words do both?
Does that help make better clusters??
Running a MiSeq
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Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
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