PANACEA: a framework to maximise genetic diversity in genome-wide association study meta-analyses
Yap, C. F.; Morris, A.
Show abstract
There have been recent efforts by the human genetics research community to increase the genetic diversity of participants contributing to genome-wide association studies (GWAS) of complex human traits and diseases. The traditional multi-ancestry GWAS approach is to first assign participants to continental ancestry labels based on their genetic similarity to individuals in reference datasets. Ancestry-specific GWAS are then conducted separately for each continental label, the results of which are aggregated through multi-ancestry meta-analysis. However, with this approach, a participant may be assigned to an ancestry group that does not reflect their personal view of ethnicity/race or may be excluded because their genetic ancestry is not sufficiently similar to individuals in reference datasets to be assigned to a single group. Here, we present a novel pipeline (PANACEA) for fully inclusive multi-ancestry meta-analysis that employs a continuous and multi-dimensional representation of ancestry that maximises the genetic diversity of GWAS. Through application to multi-ancestry GWAS of type 2 diabetes susceptibility and simulations, we demonstrate that the inclusive pooled analysis provides equivalent protection against population structure to a traditional ancestry-stratified analysis but, importantly, offers increased power to detect association through increased sample size by not excluding participants with outlying ancestry. The pooled inclusive analysis also enables assessment of ancestry-correlated heterogeneity in allelic effects without the need to assign participants to continental labels that may not sufficiently reflect genetic diversity within ancestry groups.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Evaluating Multi-Ancestry Genome-Wide Association Methods: Statistical Power, Population Structure, and Practical Implications 95%
- CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary data 95%
- A method to map and interpret pleiotropic loci using summary statistics of multiple traits 94%
Similar papers in this journal
- MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data 96%
- A new method for multi-ancestry polygenic prediction improves performance across diverse populations 95%
- Leveraging a machine learning derived surrogate phenotype to improve power for genome-wide association studies of partially missing phenotypes in population biobanks 94%
Similar papers in this journal
- A simple approach for multiple observations improves power to detect genetic effects and genomic prediction accuracy. 95%
- Inclusion of Variants Discovered from Diverse Populations Improves Polygenic Risk Score Transferability 94%
- Leveraging Global Genetics Resources to Enhance Polygenic Prediction Across Ancestrally Diverse Populations 93%
Similar papers in this journal
- Discovering genetic interactions bridging pathways in genome-wide association studies 95%
- Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits 95%
- The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup 94%
"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.