PT  - JOURNAL ARTICLE
AU  - Kerry L. Bubb
AU  - Christine Queitsch
TI  - A Two-State Epistasis Model Reduces Missing Heritability of Complex Traits
AID  - 10.1101/017491
DP  - 2016 Jan 01
TA  - bioRxiv
PG  - 017491
4099  - http://biorxiv.org/content/early/2016/03/15/017491.short
4100  - http://biorxiv.org/content/early/2016/03/15/017491.full
AB  - Despite decade-long efforts, the genetic underpinnings of many complex traits and diseases remain largely elusive. It is increasingly recognized that a purely additive model, upon which most genome-wide association studies (GWAS) rely, is insufficient. Although thousands of significant trait-associated loci have been identified, purely additive models leave much of the inferred genetic variance unexplained. Several factors have been invoked to explain the ‘missing heritability’, including epistasis. Accounting for all possible epistatic interactions is computationally complex and requires very large samples. Here, we propose a simple two-state epistasis model, in which individuals show either high or low variant penetrance with respect to a certain trait. The use of this model increases the power to detect additive trait-associated loci. We show that this model is consistent with current GWAS results and improves fit with heritability observations based on twin studies. We suggest that accounting for variant penetrance will significantly increase our power to identify underlying additive loci.