A data harmonization pipeline to leverage external controls and boost power in GWAS

Author:

Chen Danfeng1,Tashman Katherine23,Palmer Duncan S23,Neale Benjamin234,Roeder Kathryn5,Bloemendal Alex23,Churchhouse Claire234,Ke Zheng Tracy6ORCID

Affiliation:

1. Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, 08544 NJ, USA

2. Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, 02114 MA, USA

3. Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, 02142 MA, USA

4. Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, 02142 MA, USA

5. Department of Statistics, Carnegie Mellon University, Pittsburgh, 15213 PA, USA

6. Department of Statistics, Harvard University, Cambridge, 02138 MA, USA

Abstract

Abstract The use of external controls in genome-wide association study (GWAS) can significantly increase the size and diversity of the control sample, enabling high-resolution ancestry matching and enhancing the power to detect association signals. However, the aggregation of controls from multiple sources is challenging due to batch effects, difficulty in identifying genotyping errors and the use of different genotyping platforms. These obstacles have impeded the use of external controls in GWAS and can lead to spurious results if not carefully addressed. We propose a unified data harmonization pipeline that includes an iterative approach to quality control and imputation, implemented before and after merging cohorts and arrays. We apply this harmonization pipeline to aggregate 27 517 European control samples from 16 collections within dbGaP. We leverage these harmonized controls to conduct a GWAS of Crohn’s disease. We demonstrate a boost in power over using the cohort samples alone, and that our procedure results in summary statistics free of any significant batch effects. This harmonization pipeline for aggregating genotype data from multiple sources can also serve other applications where individual level genotypes, rather than summary statistics, are required.

Funder

National Institute of Mental Health

National Institute of Health

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

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