| Title: | SAIGEgds - an efficient statistical tool for large-scale PheWAS with mixed models |
| Journal: | Bioinformatics |
| Published: | 8 Sep 2020 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/32898220/ |
| DOI: | https://doi.org/10.1093/bioinformatics/btaa731 |
Publication 13694
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Abstract
SUMMARY: Phenome-wide association studies (PheWASs) are known to be a powerful tool in discovery and replication of genetic association studies. To reduce the computational burden of PheWAS in the large cohorts, such as the UK Biobank, the SAIGE method has been proposed to control for case-control imbalance and sample relatedness in a tractable manner. However, SAIGE is still computationally intensive when deployed in analyzing the associations of thousands of ICD10-coded phenotypes with whole-genome imputed genotype data. Here, we present a new high-performance statistical R package (SAIGEgds) for large-scale PheWAS using generalized linear mixed models. The package implements the SAIGE method in optimized C++ codes, taking advantage of sparse genotype dosages and integrating the efficient genomic data structure file format. Benchmarks using the UK Biobank White British genotype data (N ≈ 430 K) with coronary heart disease and simulated cases show that the implementation in SAIGEgds is 5-6 times faster than the SAIGE R package. When used in conjunction with high-performance computing clusters, SAIGEgds provides an efficient analysis pipeline for biobank-scale PheWAS.</p>
AVAILABILITY AND IMPLEMENTATION: https://bioconductor.org/packages/SAIGEgds; vignettes included.</p>
SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.</p>
5 Keywords
- Genetic Association Studies
- Genomics
- Genotype
- Phenotype
- Software
2 Authors
- Xiuwen Zheng
- J Wade Davis
Enabling scientific discoveries that improve human health