ArticleAmerican journal of human genetics2016
Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?
Article in American journal of human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.
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Who cites it
22 citing papers in PubMed, 1 synthesis or guideline pooled it.
- A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023Pooled it
- Factorizing polygenic epistasis improves prediction and uncovers biological pathways in complex traits.American journal of human genetics · 2023Article
- Cis-epistasis at the LPA locus and risk of cardiovascular diseases.Cardiovascular research · 2022Article
- Negative linkage disequilibrium between amino acid changing variants reveals interference among deleterious mutations in the human genome.PLoS genetics · 2021Article
- Article
- An enhanced machine learning tool for cis-eQTL mapping with regularization and confounder adjustments.Genetic epidemiology · 2020Article
- Modeling epistasis in mice and yeast using the proportion of two or more distinct genetic backgrounds: Evidence for "polygenic epistasis".PLoS genetics · 2020Article
- Genomics models in radiotherapy: From mechanistic to machine learning.Medical physics · 2020Review
- Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.Human molecular genetics · 2019Article
- GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations.Current genetic medicine reports · 2019Article
- Self-Adjusting Ant Colony Optimization Based on Information Entropy for Detecting Epistatic Interactions.Genes · 2019Article
- Analysis of Epistasis in Natural Traits Using Model Organisms.Trends in genetics : TIG · 2018Review
- Genetics ofeLife · 2018Article
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.Nature communications · 2018Article
- Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS.BioData mining · 2018Article
- Machine Learning and Radiogenomics: Lessons Learned and Future Directions.Frontiers in oncology · 2018Review
- Quantifying the regulatory effect size ofGenome research · 2017Article
- Widespread epistasis regulates glucose homeostasis and gene expression.PLoS genetics · 2017Article
- Enhanced methods to detect haplotypic effects on gene expression.Bioinformatics (Oxford, England) · 2017Article
- A fast algorithm for Bayesian multi-locus model in genome-wide association studies.Molecular genetics and genomics : MGG · 2017Article
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Authors and funding
3 authors.
Funding
Abstract
The importance of epistasis-or statistical interactions between genetic variants-to the development of complex disease in humans has been controversial. Genome-wide association studies of statistical interactions influencing human traits have recently become computationally feasible and have identified many putative interactions. However, statistical models used to detect interactions can be confounded, which makes it difficult to be certain that observed statistical interactions are evidence for true molecular epistasis. In this study, we investigate whether there is evidence for epistatic interactions between genetic variants within the cis-regulatory region that influence gene expression after accounting for technical, statistical, and biological confounding factors. We identified 1,119 (FDR = 5%) interactions that appear to regulate gene expression in human lymphoblastoid cell lines, a tightly controlled, largely genetically determined phenotype. Many of these interactions replicated in an independent dataset (90 of 803 tested, Bonferroni threshold). We then performed an exhaustive analysis of both known and novel confounders, including ceiling/floor effects, missing genotype combinations, haplotype effects, single variants tagged through linkage disequilibrium, and population stratification. Every interaction could be explained by at least one of these confounders, and replication in independent datasets did not protect against some confounders. Assuming that the confounding factors provide a more parsimonious explanation for each interaction, we find it unlikely that cis-regulatory interactions contribute strongly to human gene expression, which calls into question the relevance of cis-regulatory interactions for other human phenotypes. We additionally propose several best practices for epistasis testing to protect future studies from confounding.
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