Evidence map›Paper›PMID 37067493›Full record

ArticleBioinformatics (Oxford, England)2023

POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.

S Taylor Head, Elizabeth J Leslie, David J Cutler, Michael P Epstein

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

S Taylor HeadDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA 30322, United States.ORCID 0000-0002-1761-1145
Elizabeth J LeslieDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.
David J CutlerDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.
Michael P EpsteinDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, United States.ORCID 0000-0001-9647-9738

Funding

Genomic and Transcriptomic Analysis of Breast and Ovarian CancersR01CA211574 · NCI · UNIVERSITY OF VIRGINIA · PI GAYTHER, SIMON ANDREW, SCHILDKRAUT, JOELLEN M. · 2018 to 2022
$3.1M
Quantitative Genetic Models for Exploring Missing Heritability of Alzheimer's DiseaseRF1AG071170 · NIA · EMORY UNIVERSITY · PI CUTLER, DAVID JOSEPH, EPSTEIN, MICHAEL PHILIP · 2020 to 2020
$2.9M
Improved Mediation Analyses in Case-Control StudiesR21DE029698 · NIDCR · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2020 to 2021
$429k
NCI NIH HHS R01 CA211574NIA NIH HHS RF1 AG071170NIDCR NIH HHS R21 DE029698NIH HHS AG071170
6 · The paper itself

Abstract

motivationThere is widespread interest in identifying genetic variants that exhibit parent-of-origin effects (POEs) wherein the effect of an allele on phenotype expression depends on its parental origin. POEs can arise from different phenomena including genomic imprinting and have been documented for many complex traits. Traditional tests for POEs require family data to determine parental origins of transmitted alleles. As most genome-wide association studies (GWAS) sample unrelated individuals (where allelic parental origin is unknown), the study of POEs in such datasets requires sophisticated statistical methods that exploit genetic patterns we anticipate observing when POEs exist. We propose a method to improve discovery of POE variants in large-scale GWAS samples that leverages potential pleiotropy among multiple correlated traits often collected in such studies. Our method compares the phenotypic covariance matrix of heterozygotes to homozygotes based on a Robust Omnibus Test. We refer to our method as the Parent of Origin Inference using Robust Omnibus Test (POIROT) of multiple quantitative traits.

resultsThrough simulation studies, we compared POIROT to a competing univariate variance-based method which considers separate analysis of each phenotype. We observed POIROT to be well-calibrated with improved power to detect POEs compared to univariate methods. POIROT is robust to non-normality of phenotypes and can adjust for population stratification and other confounders. Finally, we applied POIROT to GWAS data from the UK Biobank using BMI and two cholesterol phenotypes. We identified 338 genome-wide significant loci for follow-up investigation. AVAILABILITY AND IMPLEMENTATION: The code for this method is available at https://github.com/staylorhead/POIROT-POE.

Indexed as

Genetic TestingGenome-Wide Association StudyComputer SimulationGenomic ImprintingPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID37067493
PMCPMC10148680

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.