Back

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

Hwang, I.; Talbot, A.; Head, T.; Trevino, C.; Wingo, T. S.; Kotlar, A. V.

2026-06-10 genetics
10.64898/2026.06.10.731310 bioRxiv
Show abstract

MotivationParent 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). ResultsWe 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 implementationThe code for this method in Python is available at https://github.com/bystrogenomics/POISE.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
Bioinformatics
1204 papers in training set
Top 2%
14.7%
2
The American Journal of Human Genetics
234 papers in training set
Top 0.3%
14.7%
3
Nature Communications
5641 papers in training set
Top 16%
11.6%
4
Nature Genetics
286 papers in training set
Top 0.7%
8.7%
5
PLOS Genetics
862 papers in training set
Top 2%
5.4%
50% of probability mass above
6
Genetic Epidemiology
55 papers in training set
Top 0.2%
3.9%
7
GENETICS
483 papers in training set
Top 1%
3.9%
8
Biometrics
23 papers in training set
Top 0.1%
3.2%
9
International Journal of Epidemiology
88 papers in training set
Top 0.5%
3.1%
10
Genome Biology
637 papers in training set
Top 4%
3.1%
11
Genome Research
468 papers in training set
Top 3%
2.3%
12
Biostatistics
24 papers in training set
Top 0.2%
2.1%
13
Nucleic Acids Research
1281 papers in training set
Top 9%
1.6%
14
PLOS Computational Biology
1863 papers in training set
Top 16%
1.4%
15
G3: Genes|Genomes|Genetics
35 papers in training set
Top 0.3%
1.1%
16
American Journal of Epidemiology
67 papers in training set
Top 1.0%
1.1%
17
eLife
5828 papers in training set
Top 59%
1.1%
18
BMC Genomics
406 papers in training set
Top 7%
1.0%
19
BMC Bioinformatics
457 papers in training set
Top 5%
1.0%
20
Proceedings of the National Academy of Sciences
2444 papers in training set
Top 39%
1.0%
21
Human Genetics and Genomics Advances
84 papers in training set
Top 2%
0.8%
22
Nature
645 papers in training set
Top 11%
0.8%
23
Statistics in Medicine
40 papers in training set
Top 0.6%
0.8%
24
Genome Medicine
183 papers in training set
Top 5%
0.8%
25
G3: Genes, Genomes, Genetics
252 papers in training set
Top 5%
0.6%
26
Nature Computational Science
55 papers in training set
Top 2%
0.6%
27
PLOS ONE
5266 papers in training set
Top 66%
0.6%