- 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
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.