Evidence map›Paper›PMID 38314848›Full record

ArticleGenetics2024

An expression-directed linear mixed model discovering low-effect genetic variants.

Qing Li, Jiayi Bian, Yanzhao Qian, Pathum Kossinna, Cooper Gau, Paul M K Gordon, Xiang Zhou, Xingyi Guo, Jun Yan, Jingjing Wu and 1 more

Abstract read
In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Qing LiDepartment of Biochemistry & Molecular Biology, University of Calgary, Calgary T2N 1N4, Canada.
Jiayi BianDepartment of Mathematics and Statistics, University of Calgary, Calgary T2N 1N4, Canada.
Yanzhao QianDepartment of Mathematics and Statistics, University of Calgary, Calgary T2N 1N4, Canada.
Pathum KossinnaDepartment of Biochemistry & Molecular Biology, University of Calgary, Calgary T2N 1N4, Canada.
Cooper GauDepartment of Mathematics and Statistics, University of Calgary, Calgary T2N 1N4, Canada.
Paul M K GordonAlberta Children's Hospital Research Institute, University of Calgary, Calgary T2N 1N4, Canada.
Xiang ZhouSchool of Public Health, University of Michigan, Ann Arbor 48109, USA.
Xingyi GuoDepartment of Medicine & Biomedical Informatics, Vanderbilt University Medical Center, Nashville 37203, USA.ORCID 0000-0001-5269-1294
Jun YanPhysiology and Pharmacology, University of Calgary, Calgary T2N 1N4, Canada.
Jingjing WuDepartment of Mathematics and Statistics, University of Calgary, Calgary T2N 1N4, Canada.
Quan LongDepartment of Biochemistry & Molecular Biology, University of Calgary, Calgary T2N 1N4, Canada.ORCID 0000-0003-3795-1873

Funding

Alberta Innovates Graduate Student ScholarshipsAlberta Innovates LevMax-Health Program Bridge Funds 222300769Campbell McLaurin Chair for Hearing DeficienciesCanada Foundation for Innovation 36605New Frontiers in Research Fund and an HBI pilot NFRFE-2018-00748NSERC Discovery RGPIN-2018-04328
6 · The paper itself

Abstract

Detecting genetic variants with low-effect sizes using a moderate sample size is difficult, hindering downstream efforts to learn pathology and estimating heritability. In this work, by utilizing informative weights learned from training genetically predicted gene expression models, we formed an alternative approach to estimate the polygenic term in a linear mixed model. Our linear mixed model estimates the genetic background by incorporating their relevance to gene expression. Our protocol, expression-directed linear mixed model, enables the discovery of subtle signals of low-effect variants using moderate sample size. By applying expression-directed linear mixed model to cohorts of around 5,000 individuals with either binary (WTCCC) or quantitative (NFBC1966) traits, we demonstrated its power gain at the low-effect end of the genetic etiology spectrum. In aggregate, the additional low-effect variants detected by expression-directed linear mixed model substantially improved estimation of missing heritability. Expression-directed linear mixed model moves precision medicine forward by accurately detecting the contribution of low-effect genetic variants to human diseases.

Indexed as

Models, GeneticMultifactorial InheritanceGenome-Wide Association StudyHumansLinear ModelsPhenotypePolymorphism, Single NucleotideSample Sizegene expressionhuman diseaseslinear mixed modellow-effect genetic variants

Identifiers

PMID38314848
PMCPMC11630775

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.