Evidence map›Paper›PMID 39974930›Full record

ArticlebioRxiv : the preprint server for biology2025

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

Xiangyu Zhang, Lijun Wang, Jia Zhao, Hongyu Zhao

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In one paragraph

Article in bioRxiv : the preprint server for biology, 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, Connecticut, United States of America.ORCID 0009-0000-2303-1588
Lijun WangDepartment of Biostatistics, School of Public Health, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0001-5222-4506
Jia ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0002-9107-8852
Hongyu ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, Connecticut, United States of America.ORCID 0000-0003-1195-9607

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
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 U24 HG012108NIGMS NIH HHS R01 GM134005
6 · The paper itself

Abstract

Transcriptome-wide association studies (TWASs) have been developed to nominate 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 evaluate the marginal association between a single gene and the trait of interest without accounting for other genes within the same genomic region or the same gene from different tissues. Additionally, false-positive gene-trait pairs can arise due to correlations with the direct effects of genetic variants. In this study, we introduce TWASKnockoff, a new knockoff-based framework for detecting causal gene-tissue pairs using GWAS summary statistics and eQTL data. Unlike marginal testing in traditional TWAS methods, TWASKnockoff examines the conditional independence for each gene-trait pair, considering both correlations in cis-predicted expression across genes and correlations between gene expression levels and genetic variants. TWASKnockoff estimates the theoretical correlation matrix for all genetic elements (cis-predicted expression across genes and genotypes for genetic variants) by averaging estimations from parametric bootstrap samples and then performs knockoff-based inference to detect causal gene-trait pairs while controlling the false discovery rate (FDR). Through empirical simulations and an application to type 2 diabetes (T2D) data, we demonstrate that TWASKnockoff achieves superior FDR control and improves the average power in detecting causal gene-trait pairs at a fixed FDR level.

Identifiers

PMID39974930
PMCPMC11838583

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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.