Evidence map›Paper›PMID 39444114›Full record

ArticleGenetic epidemiology2025

Integrative Multi-Omics Approach for Improving Causal Gene Identification.

Austin King, Chong Wu

Abstract read
In one paragraph

Article in Genetic epidemiology, 2025. 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

2 authors.

Austin KingDepartment of Statistics, Florida State University, Tallahassee, Florida, USA.ORCID http://orcid.org/0009-0008-5801-9288
Chong WuDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-8400-1785

Funding

Uncovering causal protein markers to improve prostate cancer etiology understanding and risk prediction in Africans and EuropeansR01CA263494 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI Chong Wu, Lang Wu · 2022 to 2026
$3.5M
Uncovering Causal Protein Markers to Characterize Pancreatic Cancer Etiology and Improve Risk PredictionU01CA293883 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI WU, CHONG, WU, LANG · 2024 to 2025
$1.4M
Novel Statistical Methods for Multi-omics Data Integration in Alzheimer's DiseaseR03AG070669 · NIA · FLORIDA STATE UNIVERSITY · PI BRADLEY, JONATHAN RAY, WU, CHONG · 2021 to 2022
$296k
CW is partially supported by the National Institutes of Health (1R03AG070669 and 1R01CA263494). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.NCI NIH HHS R01 CA263494NCI NIH HHS U01 CA293883NIA NIH HHS R03 AG070669
6 · The paper itself

Abstract

Transcriptome-wide association studies (TWAS) have been widely used to identify thousands of likely causal genes for diseases and complex traits using predicted expression models. However, most existing TWAS methods rely on gene expression alone and overlook other regulatory mechanisms of gene expression, including DNA methylation and splicing, that contribute to the genetic basis of these complex traits and diseases. Here we introduce a multi-omics method that integrates gene expression, DNA methylation, and splicing data to improve the identification of associated genes with our traits of interest. Through simulations and by analyzing genome-wide association study (GWAS) summary statistics for 24 complex traits, we show that our integrated method, which leverages these complementary omics biomarkers, achieves higher statistical power, and improves the accuracy of likely causal gene identification in blood tissues over individual omics methods. Finally, we apply our integrated model to a lung cancer GWAS data set, demonstrating the integrated models improved identification of prioritized genes for lung cancer risk.

Indexed as

DNA MethylationGenome-Wide Association StudyLung NeoplasmsComputer SimulationGenetic Predisposition to DiseaseGenomicsHumansModels, GeneticMultifactorial InheritanceMultiomicsPolymorphism, Single NucleotideQuantitative Trait LociTranscriptome

Identifiers

PMID39444114
PMCPMC11659073

What Socratic holds

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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 Socratic graph.