- 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
- Alzheimer’s Disease Genetics Consortium,
- Lu, Hui
- Zhao, Hongyu
- et al.
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.