Evidence map›Paper›PMID 40730164›Full record

ArticleAmerican journal of human genetics2025

Sparse matrix factorization robust to sample sharing across GWASs reveals interpretable genetic components.

Ashton R Omdahl, Joshua S Weinstock, Rebecca Keener, Surya B Chhetri, Marios Arvanitis, Alexis Battle

Abstract read
In one paragraph

Article in American journal of human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Genetic architectures of brain-related traits are shaped by strong selective constraints.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ashton R OmdahlDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Joshua S WeinstockDepartment of Human Genetics, Emory University, Atlanta, GA 30322, USA.
Rebecca KeenerDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Surya B ChhetriDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
Marios ArvanitisDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Alexis BattleDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Computer Science, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD 21218, USA; Malone Center for Engineering in Healthcare, Johns Hopkins University, Baltimore, MD 21218, USA; Data Science and AI Institute, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: ajbattle@jhu.edu.

Funding

Modeling the dynamicimpact of rare and common genetic variation on gene expression anddiseaseR35GM139580 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BATTLE, ALEXIS · 2021 to 2025
$3.1M
From genotype to phenotype in a GWAS locus: the role of REST in atherosclerosisK08HL166690 · NHLBI · OHIO STATE UNIVERSITY · PI Marios Arvanitis · 2023 to 2026
$681k
NHLBI NIH HHS K08 HL166690NIGMS NIH HHS R35 GM139580
6 · The paper itself

Abstract

Complex trait-associated genetic variation is highly pleiotropic. This extensive pleiotropy implies that multi-phenotype analyses are informative for characterizing genetic associations, as they facilitate the discovery of trait-shared and trait-specific variants and pathways ("genetic factors"). Previous efforts have estimated genetic factors using matrix factorization (MF) applied to numerous genome-wide association studies (GWASs). However, existing methods are susceptible to spurious factors arising from residual confounding due to sample sharing in biobank GWASs. Furthermore, MF approaches have historically estimated dense factors, loaded on most traits and variants, that are challenging to map onto interpretable biological pathways. To address these shortcomings, we introduce "GWAS latent embeddings accounting for noise and regularization" (GLEANR), an MF method for detection of sparse genetic factors from summary statistics. GLEANR accounts for sample sharing between studies and uses regularization to estimate a data-driven number of interpretable factors. GLEANR is robust to confounding induced by shared samples and improves the replication of genetic factors derived from distinct biobanks. We used GLEANR to evaluate 137 diverse GWASs from the UK Biobank, identifying 58 factors that decompose the genetic architecture of input traits and have distinct signatures of negative selection and degrees of polygenicity. These sparse factors can be interpreted with respect to disease, cell type, and pathway enrichment. We highlight three such factors that captured platelet-measure phenotypes and were enriched for disease-relevant markers corresponding to distinct stages of platelet differentiation. Overall, GLEANR is a powerful tool for discovering both trait-specific and trait-shared pathways underlying complex traits from GWAS summary statistics.

Indexed as

Genome-Wide Association StudyBiological Specimen BanksGenetic VariationHumansModels, GeneticMultifactorial InheritancePhenotypePolymorphism, Single NucleotideQuantitative Trait Locicohort overlapfactor analysisgenetic architecturegenomicsGWASmatrix factorizationmutli-traitpleiotropysample sharing

Identifiers

PMID40730164
PMCPMC12461026

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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.