A statistical framework for cross-tissue transcriptome-wide association analysis.
Title | A statistical framework for cross-tissue transcriptome-wide association analysis. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Hu, Y, Li, M, Lu, Q, Weng, H, Wang, J, Zekavat, SM, Yu, Z, Li, B, Gu, J, Muchnik, S, Shi, Y, Kunkle, BW, Mukherjee, S, Natarajan, P, Naj, A, Kuzma, A, Zhao, Y, Crane, PK, Lu, H, Zhao, H |
Corporate Authors | Alzheimer’s Disease Genetics Consortium, |
Journal | Nat Genet |
Volume | 51 |
Issue | 3 |
Pagination | 568-576 |
Date Published | 2019 03 |
ISSN | 1546-1718 |
Keywords | Gene Expression, Gene Expression Profiling, Genome-Wide Association Study, Genotype, Humans, Models, Genetic, Polymorphism, Single Nucleotide, Transcriptome |
Abstract | 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. |
DOI | 10.1038/s41588-019-0345-7 |
Alternate Journal | Nat Genet |
PubMed ID | 30804563 |
PubMed Central ID | PMC6788740 |
Grant List | R01 AG054060 / AG / NIA NIH HHS / United States UL1 TR000427 / TR / NCATS NIH HHS / United States U24 AG021886 / AG / NIA NIH HHS / United States U01 AG032984 / AG / NIA NIH HHS / United States K25 AG055620 / AG / NIA NIH HHS / United States R01 AG033193 / AG / NIA NIH HHS / United States T32 GM007205 / GM / NIGMS NIH HHS / United States U01 AG006781 / AG / NIA NIH HHS / United States R01 AG057508 / AG / NIA NIH HHS / United States UL1 TR002373 / TR / NCATS NIH HHS / United States / WT_ / Wellcome Trust / United Kingdom G0701075 / MRC_ / Medical Research Council / United Kingdom G0901254 / MRC_ / Medical Research Council / United Kingdom R01 GM059507 / GM / NIGMS NIH HHS / United States MR/K01417X/1 / MRC_ / Medical Research Council / United Kingdom N01AG12100 / AG / NIA NIH HHS / United States U01 AG016976 / AG / NIA NIH HHS / United States G-0907 / PUK_ / Parkinson's UK / United Kingdom R01 HL105756 / HL / NHLBI NIH HHS / United States MR/N026004/1 / MRC_ / Medical Research Council / United Kingdom R01 HL142711 / HL / NHLBI NIH HHS / United States P30 AG021342 / AG / NIA NIH HHS / United States R01 AG042437 / AG / NIA NIH HHS / United States U24 AG041689 / AG / NIA NIH HHS / United States |