A statistical framework for cross-tissue transcriptome-wide association analysis

Transcriptome-wide association analysis is a powerful approach to studying the genetic architecture of complex traits. A key component of this approach is to build a model to impute gene expression levels from genotypes by using samples with matched genotypes and gene expression data in a given tiss...

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Veröffentlicht in:Nature genetics 2019-03, Vol.51 (3), p.568-576
Hauptverfasser: Hu, Yiming, Li, Mo, Lu, Qiongshi, Weng, Haoyi, Wang, Jiawei, Zekavat, Seyedeh M., Yu, Zhaolong, Li, Boyang, Gu, Jianlei, Muchnik, Sydney, Shi, Yu, Kunkle, Brian W., Mukherjee, Shubhabrata, Natarajan, Pradeep, Naj, Adam, Kuzma, Amanda, Zhao, Yi, Crane, Paul K., Lu, Hui, Zhao, Hongyu
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Sprache:eng
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Zusammenfassung:Transcriptome-wide association analysis is a powerful approach to studying the genetic architecture of complex traits. A key component of this approach is to build a model to impute gene expression levels from genotypes by using samples with matched genotypes and gene expression data in a given tissue. However, it is challenging to develop robust and accurate imputation models with a limited sample size for any single tissue. Here, we first introduce a multi-task learning method to jointly impute gene expression in 44 human tissues. Compared with single-tissue methods, our approach achieved an average of 39% improvement in imputation accuracy and generated effective imputation models for an average of 120% more genes. We describe a summary-statistic-based testing framework that combines multiple single-tissue associations into a powerful metric to quantify the overall gene–trait association. We applied our method, called UTMOST (unified test for molecular signatures), to multiple genome-wide-association results and demonstrate its advantages over single-tissue strategies. UTMOST (unified test for molecular signatures) is a method for cross-tissue gene expression imputation for transcriptome-wide association analyses. Cross-tissue TWAS using UTMOST identifies new candidate genes for late-onset Alzheimer’s disease.
ISSN:1061-4036
1546-1718
1546-1718
DOI:10.1038/s41588-019-0345-7