Re-analysis and meta-analysis of summary statistics from gene–environment interaction studies

Author:

Pham Duy T1ORCID,Westerman Kenneth E234,Pan Cong1,Chen Ling23,Srinivasan Shylaja5ORCID,Isganaitis Elvira6ORCID,Vajravelu Mary Ellen7,Bacha Fida8ORCID,Chernausek Steve9,Gubitosi-Klug Rose10,Divers Jasmin11,Pihoker Catherine12,Marcovina Santica M13,Manning Alisa K234,Chen Han1ORCID

Affiliation:

1. Human Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston , Houston, TX 77030, United States

2. Department of Medicine, Clinical and Translational Epidemiology Unit, Mongan Institute, Massachusetts General Hospital , Boston, MA 02114, United States

3. Metabolism Program, Broad Institute of MIT and Harvard , Cambridge, MA 02142, United States

4. Department of Medicine, Harvard Medical School , Boston, MA 02115, United States

5. Department of Pediatrics, University of California , San Francisco, CA 94158, United States

6. Research Division, Joslin Diabetes Center , Boston, MA 02115, United States

7. Department of Pediatrics, University of Pittsburgh School of Medicine , Pittsburgh, PA 15224, United States

8. Department of Pediatrics, Baylor College of Medicine , Houston, TX 77030, United States

9. Department of Pediatrics, The University of Oklahoma College of Medicine , Oklahoma City, OK 73117, United States

10. Department of Pediatrics, Case Western Reserve University , Cleveland, OH 44106, United States

11. Department of Foundations of Medicine, New York University , New York, NY 10016, United States

12. Department of Pediatrics, University of Washington School of Medicine , Seattle, WA 98105, United States

13. Northwest Lipid Metabolism and Diabetes Research Laboratories, Department of Medicine, University of Washington , Seattle, WA 98105, United States

Abstract

Abstract Motivation Summary statistics from genome-wide association studies enable many valuable downstream analyses that are more efficient than individual-level data analysis while also reducing privacy concerns. As growing sample sizes enable better-powered analysis of gene–environment interactions, there is a need for gene–environment interaction-specific methods that manipulate and use summary statistics. Results We introduce two tools to facilitate such analysis, with a focus on statistical models containing multiple gene–exposure and/or gene–covariate interaction terms. REGEM (RE-analysis of GEM summary statistics) uses summary statistics from a single, multi-exposure genome-wide interaction study to derive analogous sets of summary statistics with arbitrary sets of exposures and interaction covariate adjustments. METAGEM (META-analysis of GEM summary statistics) extends current fixed-effects meta-analysis models to incorporate multiple exposures from multiple studies. We demonstrate the value and efficiency of these tools by exploring alternative methods of accounting for ancestry-related population stratification in genome-wide interaction study in the UK Biobank as well as by conducting a multi-exposure genome-wide interaction study meta-analysis in cohorts from the diabetes-focused ProDiGY consortium. These programs help to maximize the value of summary statistics from diverse and complex gene–environment interaction studies. Availability and implementation REGEM and METAGEM are open-source projects freely available at https://github.com/large-scale-gxe-methods/REGEM and https://github.com/large-scale-gxe-methods/METAGEM.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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