插补(统计学)
生物
计算生物学
遗传关联
全基因组关联研究
统计的
遗传建筑学
表达数量性状基因座
公制(单位)
特质
基因
计算机科学
数量性状位点
数据挖掘
遗传学
基因型
统计
机器学习
缺少数据
单核苷酸多态性
数学
经济
运营管理
程序设计语言
作者
Yiming Hu,Mo Li,Qiongshi Lu,Haoyi Weng,Jiawei Wang,Seyedeh M. Zekavat,Zhaolong Yu,Boyang Li,Jianlei Gu,Sydney Muchnik,Yu Shi,Brian W. Kunkle,Shubhabrata Mukherjee,Pradeep Natarajan,Adam C. Naj,Amanda Kuzma,Yi Zhao,Paul K. Crane,Hui Lü,Hongyu Zhao
出处
期刊:Nature Genetics
[Springer Nature]
日期:2019-02-25
卷期号:51 (3): 568-576
被引量:285
标识
DOI:10.1038/s41588-019-0345-7
摘要
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.
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