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Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data.

Publication ,  Journal Article
Gurinovich, A; Li, M; Leshchyk, A; Bae, H; Song, Z; Arbeev, KG; Nygaard, M; Feitosa, MF; Perls, TT; Sebastiani, P
Published in: Frontiers in genetics
January 2022

Performing a genome-wide association study (GWAS) with a binary phenotype using family data is a challenging task. Using linear mixed effects models is typically unsuitable for binary traits, and numerical approximations of the likelihood function may not work well with rare genetic variants with small counts. Additionally, imbalance in the case-control ratios poses challenges as traditional statistical methods such as the Score test or Wald test perform poorly in this setting. In the last couple of years, several methods have been proposed to better approximate the likelihood function of a mixed effects logistic regression model that uses Saddle Point Approximation (SPA). SPA adjustment has recently been implemented in multiple software, including GENESIS, SAIGE, REGENIE and fastGWA-GLMM: four increasingly popular tools to perform GWAS of binary traits. We compare Score and SPA tests using real family data to evaluate computational efficiency and the agreement of the results. Additionally, we compare various ways to adjust for family relatedness, such as sparse and full genetic relationship matrices (GRM) and polygenic effect estimates. We use the New England Centenarian Study imputed genotype data and the Long Life Family Study whole-genome sequencing data and the binary phenotype of human extreme longevity to compare the agreement of the results and tools' computational performance. The evaluation suggests that REGENIE might not be a good choice when analyzing correlated data of a small size. fastGWA-GLMM is the most computationally efficient compared to the other three tools, but it appears to be overly conservative when applied to family-based data. GENESIS, SAIGE and fastGWA-GLMM produced similar, although not identical, results, with SPA adjustment performing better than Score tests. Our evaluation also demonstrates the importance of adjusting by full GRM in highly correlated datasets when using GENESIS or SAIGE.

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Published In

Frontiers in genetics

DOI

EISSN

1664-8021

ISSN

1664-8021

Publication Date

January 2022

Volume

13

Start / End Page

897210

Related Subject Headings

  • 3105 Genetics
  • 1801 Law
  • 1103 Clinical Sciences
  • 0604 Genetics
 

Citation

APA
Chicago
ICMJE
MLA
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Gurinovich, A., Li, M., Leshchyk, A., Bae, H., Song, Z., Arbeev, K. G., … Sebastiani, P. (2022). Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data. Frontiers in Genetics, 13, 897210. https://doi.org/10.3389/fgene.2022.897210
Gurinovich, Anastasia, Mengze Li, Anastasia Leshchyk, Harold Bae, Zeyuan Song, Konstantin G. Arbeev, Marianne Nygaard, Mary F. Feitosa, Thomas T. Perls, and Paola Sebastiani. “Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data.Frontiers in Genetics 13 (January 2022): 897210. https://doi.org/10.3389/fgene.2022.897210.
Gurinovich A, Li M, Leshchyk A, Bae H, Song Z, Arbeev KG, et al. Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data. Frontiers in genetics. 2022 Jan;13:897210.
Gurinovich, Anastasia, et al. “Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data.Frontiers in Genetics, vol. 13, Jan. 2022, p. 897210. Epmc, doi:10.3389/fgene.2022.897210.
Gurinovich A, Li M, Leshchyk A, Bae H, Song Z, Arbeev KG, Nygaard M, Feitosa MF, Perls TT, Sebastiani P. Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data. Frontiers in genetics. 2022 Jan;13:897210.

Published In

Frontiers in genetics

DOI

EISSN

1664-8021

ISSN

1664-8021

Publication Date

January 2022

Volume

13

Start / End Page

897210

Related Subject Headings

  • 3105 Genetics
  • 1801 Law
  • 1103 Clinical Sciences
  • 0604 Genetics