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. 2013 Sep 25;42(2):e8. doi: 10.1093/nar/gkt865

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© The Author(s) 2013. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — LI library preparation quality control. Two examples of fragmented human genomic samples to a target of 900 bp are shown (A). Fragmented samples are run alongside Invitrogen’s 1 Kb Plus DNA ladder. An example of ligation products for the LI-WGS preparation protocol is shown in (B). Products are run alongside the same 1 Kb Plus ladder shown in (C). The same gel from (B) following size selection is shown in (C) in which multiple collections of ligation product were obtained. An example Bioanalyzer trace of a final LI-WGS library is shown in (D; FU = fluorescence units). The library peak is demarcated by an arrow; flanking peaks are Bioanalyzer marker peaks.