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Article: TransferTWAS: A transfer learning framework for cross-tissue transcriptome-wide association study

TitleTransferTWAS: A transfer learning framework for cross-tissue transcriptome-wide association study
Authors
KeywordseQTLs
genetic association
genome-wide association studies
transcriptome-wide association study
transfer learning
Issue Date7-Aug-2025
PublisherCell Press
Citation
American Journal of Human Genetics, 2025, v. 112, n. 8, p. 1936-1947 How to Cite?
Abstract

Transcriptome-wide association studies (TWASs) utilize gene-expression data to explore the genetic basis of complex traits. A key challenge in TWASs is developing robust imputation models for tissues with limited sample sizes. This paper introduces transfer learning-assisted TWAS (TransferTWAS), a framework that adaptively transfers information from multiple tissues to improve gene-expression prediction in the target tissue. TransferTWAS employs a data-driven strategy that assigns higher weights to genetically similar external tissues. It outperforms other multi-tissue TWAS methods, such as the Unified Test for Molecular Signatures (UTMOST), which neglects tissue similarity, and Joint-Tissue Imputation (JTI), which relies on functional annotations to represent tissue similarity. Simulation studies demonstrate that TransferTWAS achieves the highest imputation accuracy, and analyses using the ROS/MAP and GEUVADIS datasets show a substantial power gain while maintaining control over type-I errors. Furthermore, analysis of the low-density lipoprotein cholesterol GWAS dataset and other complex traits demonstrates that TransferTWAS effectively identifies more associations compared with existing methods.


Persistent Identifierhttp://hdl.handle.net/10722/358695
ISSN
2023 Impact Factor: 8.1
2023 SCImago Journal Rankings: 4.516

 

DC FieldValueLanguage
dc.contributor.authorLai, Daoyuan-
dc.contributor.authorWang, Han-
dc.contributor.authorGu, Tian-
dc.contributor.authorWu, Siqi-
dc.contributor.authorLiu, Dajiang J.-
dc.contributor.authorSham, Pak Chung-
dc.contributor.authorZhang, Yan Dora-
dc.date.accessioned2025-08-13T07:47:28Z-
dc.date.available2025-08-13T07:47:28Z-
dc.date.issued2025-08-07-
dc.identifier.citationAmerican Journal of Human Genetics, 2025, v. 112, n. 8, p. 1936-1947-
dc.identifier.issn0002-9297-
dc.identifier.urihttp://hdl.handle.net/10722/358695-
dc.description.abstract<p>Transcriptome-wide association studies (TWASs) utilize gene-expression data to explore the genetic basis of complex traits. A key challenge in TWASs is developing robust imputation models for tissues with limited sample sizes. This paper introduces transfer learning-assisted TWAS (TransferTWAS), a framework that adaptively transfers information from multiple tissues to improve gene-expression prediction in the target tissue. TransferTWAS employs a data-driven strategy that assigns higher weights to genetically similar external tissues. It outperforms other multi-tissue TWAS methods, such as the Unified Test for Molecular Signatures (UTMOST), which neglects tissue similarity, and Joint-Tissue Imputation (JTI), which relies on functional annotations to represent tissue similarity. Simulation studies demonstrate that TransferTWAS achieves the highest imputation accuracy, and analyses using the ROS/MAP and GEUVADIS datasets show a substantial power gain while maintaining control over type-I errors. Furthermore, analysis of the low-density lipoprotein cholesterol GWAS dataset and other complex traits demonstrates that TransferTWAS effectively identifies more associations compared with existing methods.</p>-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofAmerican Journal of Human Genetics-
dc.subjecteQTLs-
dc.subjectgenetic association-
dc.subjectgenome-wide association studies-
dc.subjecttranscriptome-wide association study-
dc.subjecttransfer learning-
dc.titleTransferTWAS: A transfer learning framework for cross-tissue transcriptome-wide association study -
dc.typeArticle-
dc.identifier.doi10.1016/j.ajhg.2025.06.006-
dc.identifier.scopuseid_2-s2.0-105009516274-
dc.identifier.volume112-
dc.identifier.issue8-
dc.identifier.spage1936-
dc.identifier.epage1947-
dc.identifier.eissn1537-6605-
dc.identifier.issnl0002-9297-

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