Identifying latent genetic interactions in genome-wide association studies using multiple traits.
Andrew J BassShijia BianAliza P WingoThomas S WingoDavid J CutlerMichael P EpsteinPublished in: Genome medicine (2024)
The "missing" heritability of complex traits may be partly explained by genetic variants interacting with other genes or environments that are difficult to specify, observe, and detect. We propose a new kernel-based method called Latent Interaction Testing (LIT) to screen for genetic interactions that leverages pleiotropy from multiple related traits without requiring the interacting variable to be specified or observed. Using simulated data, we demonstrate that LIT increases power to detect latent genetic interactions compared to univariate methods. We then apply LIT to obesity-related traits in the UK Biobank and detect variants with interactive effects near known obesity-related genes (URL: https://CRAN.R-project.org/package=lit ).
Keyphrases
- genome wide
- copy number
- dna methylation
- genome wide association
- insulin resistance
- metabolic syndrome
- weight loss
- type diabetes
- weight gain
- high fat diet induced
- high throughput
- protein kinase
- quality improvement
- machine learning
- gene expression
- adipose tissue
- skeletal muscle
- body mass index
- big data
- transcription factor
- data analysis