I'd like to know how efficiently to do the size-selection of library ligated with TruSeq adapter from the Gel-method.
TruSeq adapter has very long non-hybridized Y-shape form (about 50 nt X 2 = 100 nt at both ends).
Have you had any different results regarding the size of library between size-selection after ligation with adapter and final PCR amplification?
TruSeq adapter has very long non-hybridized Y-shape form (about 50 nt X 2 = 100 nt at both ends).
Have you had any different results regarding the size of library between size-selection after ligation with adapter and final PCR amplification?
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