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Article: TWAS-GKF: a novel method for causal gene identification in transcriptome-wide association studies with knockoff inference

TitleTWAS-GKF: a novel method for causal gene identification in transcriptome-wide association studies with knockoff inference
Authors
Issue Date1-Aug-2024
PublisherOxford University Press
Citation
Bioinformatics, 2024, v. 40, n. 8 How to Cite?
Abstract

Motivation: Transcriptome-wide association study (TWAS) aims to identify trait-associated genes regulated by significant variants to explore the underlying biological mechanisms at a tissue-specific level. Despite the advancement of current TWAS methods to cover diverse traits, traditional approaches still face two main challenges: (i) the lack of methods that can guarantee finite-sample false discovery rate (FDR) control in identifying trait-associated genes; and (ii) the requirement for individual-level data, which is often inaccessible. Results: To address this challenge, we propose a powerful knockoff inference method termed TWAS-GKF to identify candidate trait-associated genes with a guaranteed finite-sample FDR control. TWAS-GKF introduces the main idea of Ghostknockoff inference to generate knockoff variables using only summary statistics instead of individual-level data. In extensive studies, we demonstrate that TWAS-GKF successfully controls the finite-sample FDR under a pre-specified FDR level across all settings. We further apply TWAS-GKF to identify genes in brain cerebellum tissue from the Genotype-Tissue Expression (GTEx) v8 project associated with schizophrenia (SCZ) from the Psychiatric Genomics Consortium (PGC), and genes in liver tissue related to low-density lipoprotein cholesterol (LDL-C) from the UK Biobank, respectively. The results reveal that the majority of the identified genes are validated by Open Targets Validation Platform.


Persistent Identifierhttp://hdl.handle.net/10722/356781
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, Anqi-
dc.contributor.authorTian, Peixin-
dc.contributor.authorZhang, Yan Dora-
dc.date.accessioned2025-06-17T00:35:17Z-
dc.date.available2025-06-17T00:35:17Z-
dc.date.issued2024-08-01-
dc.identifier.citationBioinformatics, 2024, v. 40, n. 8-
dc.identifier.urihttp://hdl.handle.net/10722/356781-
dc.description.abstract<p>Motivation: Transcriptome-wide association study (TWAS) aims to identify trait-associated genes regulated by significant variants to explore the underlying biological mechanisms at a tissue-specific level. Despite the advancement of current TWAS methods to cover diverse traits, traditional approaches still face two main challenges: (i) the lack of methods that can guarantee finite-sample false discovery rate (FDR) control in identifying trait-associated genes; and (ii) the requirement for individual-level data, which is often inaccessible. Results: To address this challenge, we propose a powerful knockoff inference method termed TWAS-GKF to identify candidate trait-associated genes with a guaranteed finite-sample FDR control. TWAS-GKF introduces the main idea of Ghostknockoff inference to generate knockoff variables using only summary statistics instead of individual-level data. In extensive studies, we demonstrate that TWAS-GKF successfully controls the finite-sample FDR under a pre-specified FDR level across all settings. We further apply TWAS-GKF to identify genes in brain cerebellum tissue from the Genotype-Tissue Expression (GTEx) v8 project associated with schizophrenia (SCZ) from the Psychiatric Genomics Consortium (PGC), and genes in liver tissue related to low-density lipoprotein cholesterol (LDL-C) from the UK Biobank, respectively. The results reveal that the majority of the identified genes are validated by Open Targets Validation Platform.</p>-
dc.languageeng-
dc.publisherOxford University Press-
dc.relation.ispartofBioinformatics-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleTWAS-GKF: a novel method for causal gene identification in transcriptome-wide association studies with knockoff inference-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1093/bioinformatics/btae502-
dc.identifier.pmid39189955-
dc.identifier.scopuseid_2-s2.0-85202847700-
dc.identifier.volume40-
dc.identifier.issue8-
dc.identifier.eissn1367-4811-
dc.identifier.isiWOS:001300235400002-
dc.identifier.issnl1367-4803-

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