ArticleStatistical applications in genetics and molecular biology2011
Multiple imputation of missing phenotype data for QTL mapping.
Article in Statistical applications in genetics and molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.
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Who cites it
5 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Imputing Phenotypes for Genome-wide Association Studies.American journal of human genetics · 2016Pooled it
- Mapping novel genetic loci associated with female liver weight variations using Collaborative Cross mice.Animal models and experimental medicine · 2018Article
- In silico phenotyping via co-training for improved phenotype prediction from genotype.Bioinformatics (Oxford, England) · 2015Article
- Genome-wide association study based on multiple imputation with low-depth sequencing data: application to biofuel traits in reed canarygrass.G3 (Bethesda, Md.) · 2015Article
- Probability genotype imputation method and integrated weighted lasso for QTL identification.BMC genetics · 2013Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Missing phenotype data can be a major hurdle to mapping quantitative trait loci (QTL).Though in many cases experiments may be designed to minimize the occurrence of missing data,it is often unavoidable in practice; thus, statistical methods to account for missing data are needed.In this paper we describe an approach for conjoining multiple imputation and QTL mapping.Methods are applied to map genes associated with increased breathing effort in mice after lung inflammation due to allergen challenge in developing lines of the Collaborative Cross, a new mouse genetics resource. Missing data poses a particular challenge in this study because the desired phenotype summary to be mapped is a function of incompletely observed dose-response curves. Comparison of the multiple imputation approach to two naive approaches for handling missing data suggest that these simpler methods may yield poor results: ignoring missing data through a complete case analysis may lead to incorrect conclusions, while using a last observation carried forward procedure, which does not account for uncertainty in the imputed values, may lead to anti-conservative inference. The proposed approach is widely applicable to other studies with missing phenotype data.
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Registered trials
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