Evidence map›Paper›PMID 40902598›Full record

ArticleAmerican journal of human genetics2025

Knockoff procedure improves susceptibility gene identifications in conditional transcriptome-wide association studies.

Xiangyu Zhang, Lijun Wang, Jia Zhao, Hongyu Zhao

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. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiangyu ZhangDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.
Lijun WangDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.
Jia ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.
Hongyu ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA. Electronic address: hongyu.zhao@yale.edu.

Funding

Laboratory, Data Analysis, and Coordinating Center (LDACC) for the Developmental Human Genotype-Tissue Expression ProjectU24HG012108 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, HUTTNER, ANITA JULIANE · 2021 to 2025
$8.7M
Computational and Statistical Methods to determine variant effect across cell types and development stagesU01HG013840 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, ZHAO, HONGYU · 2024 to 2024
$1.9M
Novel statistical methods and tools to integrate multiple endophenotypes and functional annotation data to study the roles of rare variants in complex human diseases using sequencing dataR01GM134005 · NIGMS · YALE UNIVERSITY · PI WU, BAOLIN, ZHAO, HONGYU · 2020 to 2023
$1.6M
NHGRI NIH HHS U01 HG013840NHGRI NIH HHS U24 HG012108NIGMS NIH HHS R01 GM134005
6 · The paper itself

Abstract

Transcriptome-wide association studies (TWASs) have been developed to identify candidate genes associated with complex traits by integrating genome-wide association studies (GWASs) with expression quantitative trait loci (eQTL) data. However, most existing TWAS methods assess the marginal association between a single gene and a trait of interest, ignoring the influence of other genes in the same genomic region. Furthermore, false-positive gene-trait associations may arise due to correlations between eQTLs and nearby causal genetic variants. We introduce TWASKnockoff, a knockoff-based framework for detecting susceptibility genes using GWAS summary statistics and eQTL data. Unlike traditional TWAS approaches that rely on marginal testing, TWASKnockoff evaluates the conditional independence of each gene-trait pair, accounting for both cis-predicted expression correlations across genes and correlations between gene expression levels and genetic variants. TWASKnockoff estimates the correlation matrix of all genetic elements (including cis-predicted gene expression levels and genetic variant genotypes) by averaging estimations from parametric bootstrap samples, then applies knockoff-based inference to identify susceptibility genes while controlling the false discovery rate (FDR). Through simulations and an application to type 2 diabetes mellitus (T2D) data, we demonstrate that TWASKnockoff achieves superior FDR control and enhances power in detecting relevant gene-trait pairs at a fixed FDR level.

Indexed as

Genetic Predisposition to DiseaseTranscriptomeDatasets as TopicDiabetes Mellitus, Type 2Gene Expression ProfilingGenome-Wide Association StudyGenotypeHumansQuantitative Trait LociRisk Factorsexpression quantitative trait locifalse discovery rate controlknockoffssusceptibility genetranscriptome-wide association studies

Identifiers

PMID40902598
PMCPMC12412983

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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.