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S. Taylor Head

dblp:370/4843 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2023
0000-0002-1761-1145ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genome-wide association study
0.712023
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes · Bioinform. 2023
Bioinformatics and computational biology
genomics
0.712023
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes · Bioinform. 2023
Bioinformatics and computational biology › genomics › genome-wide association study
multi-trait association testing
0.712023
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics › genotype-phenotype analysis
pleiotropy analysis
0.712023
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes · Bioinform. 2023

Methods — techniques the papers use, named apart from their topics

robust omnibus test · 0.7phenotypic covariance comparison · 0.7
YearPublicationVenuePosition
2023 POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes
abstract
MOTIVATION: There 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. RESULTS: Through 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.
S. Taylor Head, Elizabeth J. Leslie, David J. Cutler, Michael P. Epstein
Bioinform.1