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. 2015 Oct 12;10(11):1024–1032. doi: 10.1080/15592294.2015.1100786

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© 2015 The Author(s). Published with license by Taylor & Francis Group, LLC

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 use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

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Figure 5. — EWAS analyses of brain phenotypes using whole blood DNA may potentially miss disease associated variation and interrogate DNA methylation sites that are not actually variable in the brain. Venn diagrams showing the overlap of DNA methylation sites that are (A) variable in whole blood but not variable in the cortex (STG) or cerebellum and (B) variable in the cortex (STG) and cerebellum but not in whole blood.