Assess library quality on a Bioanalyzer® (Agilent high sensitivity chip) (E7530)

Protocol

1. Dilute (1:4) library in nuclease-free water.
   
   
2. Run 1 μl in a DNA High Sensitivity chip.
   
   
3. Check that the electropherogram shows a narrow distribution with a peak size approximately 300 bp.

Note: If a peak at ~ 80 bp (primers) or 128 bp (adaptor-dimer) is shown in the bioanalyzer traces; Bring up the sample volume to 50 μl exactly with nuclease-free water and repeat the AMPure XP bead clean up step.