Detecting genotype-population interaction effects by ancestry principal components
Yu, C.; Ni, G.; van der Werf, J.; Lee, S. H.
Show abstract
Heterogeneity in the phenotypic mean and variance across populations is often observed for complex traits. One way to understand heterogeneous phenotypes lies in uncovering heterogeneity in genetic effects. Previous studies on genetic heterogeneity across populations were typically based on discrete groups of population stratified by different countries or cohorts, which ignored the difference of population characteristics for the individuals within each group and resulted in loss of information. Here we introduce a novel concept of genotype-by-population (GxP) interaction where population is defined by the first and second ancestry principal components (PCs), which are less likely to be confounded with country/cohort-specific factors. We applied a reaction norm model fitting each of 70 complex traits with significant SNP-heritability and the PCs as covariates to examine GxP interactions across diverse populations including white British and other white Europeans from the UK Biobank (N = 22,229). Our results demonstrated a significant population genetic heterogeneity for behavioural traits such as age first had sexual intercourse and qualifications. Our approach may shed light on the latent genetic architecture of complex traits that underlies the modulation of genetic effects across different populations.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Quantifying genetic heterogeneity between continental populations for human height and body mass index 96%
- Controlling for background genetic effects using polygenic scores improves the power of genome-wide association studies 95%
- Controlling for Human Population Stratification in Rare Variant Association Studies 94%
Similar papers in this journal
- Significance tests for R2 of out-of-sample prediction using polygenic scores 97%
- Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals 96%
- Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction 94%
Similar papers in this journal
- Inclusion of Variants Discovered from Diverse Populations Improves Polygenic Risk Score Transferability 95%
- Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations 94%
- A reference panel for linkage disequilibrium and genotype imputation using whole-genome sequencing data from 2,680 participants across India 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.