Evidence map›Paper›PMID 42327059›Full record

ArticlebioRxiv : the preprint server for biology2026

POISE: Spectral Inference of Parent-of-Origin Effects in Unlabeled Genomic Data.

Ilha Hwang, Austin Talbot, S Taylor Head, Cristina Trevino, Thomas S Wingo, Alex Kotlar

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ilha HwangDepartment of Mathematics, Brigham Young University, 275 TMCB Provo, Utah, 84604 USA.
Austin TalbotDepartment of Human Genetics, Emory University, 615 Michael Street Atlanta, GA, 30322, USA.ORCID 0000-0001-6207-1304
S Taylor HeadDepartment of Epidemiology, University of Texas MD Anderson Cancer Center, 1155 Pressler Street Houston, Texas, 77030, USA.ORCID 0000-0002-1761-1145
Cristina TrevinoDepartment of Human Genetics, Emory University, 615 Michael Street Atlanta, GA, 30322, USA.ORCID 0000-0002-9851-7547
Thomas S WingoDepartment of Neurology, UC Davis School of Medicine, 1544 Newton Court Davis, CA, 95618, USA.ORCID 0000-0002-7679-6282
Alex KotlarDepartment of Human Genetics, Emory University, 615 Michael Street Atlanta, GA, 30322, USA.ORCID 0000-0002-1578-6849

Funding

The Goizueta Alzheimer's Disease Research CenterP30AG066511 · NIA · EMORY UNIVERSITY · PI ALLAN I LEVEY · 2020 to 2026
$29.0M
NIA NIH HHS P30 AG066511
6 · The paper itself

Abstract

Motivation: Parent of Origin Effects (POEs), where the effect of an an allele on a phenotype differs based on maternal or paternal inheritance implicated in growth, metabolism, and neurodevelopment. Traditional tests for POEs require family data to determine parental origins of transmitted alleles. Given that such studies are expensive and time consuming compared to genome-wide association studies (GWAS), tests that function absent inheritance information are highly desirable. We develop a method, based on community detection from machine learning, that infers POEs via a spectral decomposition, obtains confidence intervals via a non-parametric bootstrap, and safeguards against confounding by non POE sources of variation. We refer to our method as Parent of Origin Inference via Spectral Estimation (POISE). Results: We demonstrate that POISE is well-calibrated under both Gaussian and heavy-tailed noise in simulation studies, with improved robustness to true POEs compared to existing covariance-based tests. POISE provides per-trait effect estimates with bias-corrected bootstrap confidence intervals and incorporates an information-theoretic minimum detectable effect size that filters unreliable estimates, conferring robustness to covariance-deflating variance QTL. We then apply POISE to GWAS data from the UK Biobank using BMI, LDL cholesterol, and HDL cholesterol. POISE recovers established POE loci and identifies 134 additional variants at genes implicated in lipid metabolism, immune regulation, and growth. Availability and implementation: The code for this method in Python is available at https://github.com/bystrogenomics/POISE.

Indexed as

Community DetectionGenome Wide Association StudiesParent of Origin EffectSpectral AnalysisSpectral estimationStatistical Bootstrap

Identifiers

PMID42327059
PMCPMC13277854

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.