# Latent epistatic interaction model identifies loci associated with human working memory

## TL;DR

This paper introduces a new method to detect gene interactions that influence human working memory, improving efficiency and accuracy over existing approaches.

## Contribution

A novel latent interaction-based selection method is introduced for efficient epistasis detection in genome-wide studies.

## Key findings

- The new method outperforms existing approaches in detecting epistatic interactions, especially in the presence of linkage disequilibrium.
- When applied to real human genotype data, the method identified SNP pairs associated with working memory performance.
- The proposed approach reduces computational complexity and increases statistical power for genome-wide epistasis detection.

## Abstract

Epistatic interactions among genomic loci are expected to explain a large fraction of the heritability of complex diseases and phenotypic traits of living organisms.

Although epistasis detection methods are continually being developed, the current state of the art is exhaustive search methods, which become infeasible when the number of analyzed loci is large.

We develop a novel latent interaction-based selection method for polymorphic loci as the first stage of a two-stage epistasis detection approach. Given a continuous phenotype and a single-nucleotide polymorphism (SNP), we rank the SNPs according to their interaction potential. When tested on simulated datasets and compared to standard marginal association and exhaustive search methods, our procedure significantly outperforms main-effect heuristics, especially in the presence of linkage disequilibrium (LD), which is explicitly accounted for in our model. Applied to real human genotype data, we prioritized several SNP pairs as candidates for epistatic interactions that influence human working memory performance, some of which are known to be connected to this phenotype.

The proposed method improves two-stage epistasis detection. Its linear runtime and increased statistical power contribute to reducing the computational complexity and to addressing some of the statistical challenges associated with the genome-wide search for epistatic loci.