ArticleJournal of the American Statistical Association2019
Robust Score Tests With Missing Data in Genomics Studies.
Article in Journal of the American Statistical Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- vcfsim: flexible simulation of all-sites VCFs with missing data.BMC bioinformatics · 2026Article
- Chimeric reference panels for genomic imputation.Genetics · 2026Article
- vcfsim: flexible simulation of all-sites VCFs with missing data.bioRxiv : the preprint server for biology · 2025Article
- Missing Values in Longitudinal Proteome Dynamics Studies: Making a Case for Data Multiple Imputation.Journal of proteome research · 2024Article
- Two-phase sample selection strategies for design and analysis in post-genome-wide association fine-mapping studies.Statistics in medicine · 2021Article
- pixy: Unbiased estimation of nucleotide diversity and divergence in the presence of missing data.Molecular ecology resources · 2021Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Analysis of genomic data is often complicated by the presence of missing values, which may arise due to cost or other reasons. The prevailing approach of single imputation is generally invalid if the imputation model is misspecified. In this paper, we propose a robust score statistic based on imputed data for testing the association between a phenotype and a genomic variable with (partially) missing values. We fit a semiparametric regression model for the genomic variable against an arbitrary function of the linear predictor in the phenotype model and impute each missing value by its estimated posterior expectation. We show that the score statistic with such imputed values is asymptotically unbiased under general missing-data mechanisms, even when the imputation model is misspecified. We develop a spline-based method to estimate the semiparametric imputation model and derive the asymptotic distribution of the corresponding score statistic with a consistent variance estimator using sieve approximation theory and empirical process theory. The proposed test is computationally feasible regardless of the number of independent variables in the imputation model. We demonstrate the advantages of the proposed method over existing methods through extensive simulation studies and provide an application to a major cancer genomics study.
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Registered trials
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