4.8 Article

Mendelian imputation of parental genotypes improves estimates of direct genetic effects

Journal

NATURE GENETICS
Volume 54, Issue 6, Pages 897-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41588-022-01085-0

Keywords

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Funding

  1. Li Ka Shing Foundation
  2. Open Philanthropy [010623-00001, 2019-198171]
  3. Netherlands Organisation for Scientific Research (VENI grant) [016.Veni.198.058]
  4. National Institute on Aging/National Institutes of Health [R24-AG065184, R01-AG042568, K99-AG062787-01, R00-AG062787, R21-AG067585]

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This study introduces a method that imputes missing parental genotypes and estimates direct genetic effects to address confounding bias in standard GWASs. Using UK Biobank data, the results demonstrate substantial confounding bias in standard GWASs for some phenotypes.
Effects estimated by genome-wide association studies (GWASs) include effects of alleles in an individual on that individual (direct genetic effects), indirect genetic effects (for example, effects of alleles in parents on offspring through the environment) and bias from confounding. Within-family genetic variation is random, enabling unbiased estimation of direct genetic effects when parents are genotyped. However, parental genotypes are often missing. We introduce a method that imputes missing parental genotypes and estimates direct genetic effects. Our method, implemented in the software package snipar (single-nucleotide imputation of parents), gives more precise estimates of direct genetic effects than existing approaches. Using 39,614 individuals from the UK Biobank with at least one genotyped sibling/parent, we estimate the correlation between direct genetic effects and effects from standard GWASs for nine phenotypes, including educational attainment (r = 0.739, standard error (s.e.) = 0.086) and cognitive ability (r = 0.490, s.e. = 0.086). Our results demonstrate substantial confounding bias in standard GWASs for some phenotypes. snipar is a software package for imputing missing parental genotypes and estimating direct genetic effects. Application to UK Biobank data shows that effects estimated by standard genome-wide association study designs have confounding bias for some phenotypes.

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