Knockoff procedure improves causal gene identifications in conditional transcriptome-wide association studies
Zhang, X.; Wang, L.; Zhao, J.; Zhao, H.
Show abstract
Transcriptome-wide association studies (TWASs) have been developed to nominate candidate genes associated with complex traits by integrating genome-wide association studies (GWASs) with expression quantitative trait loci (eQTL) data. However, most existing TWAS methods evaluate the marginal association between a single gene and the trait of interest without accounting for other genes within the same genomic region or the same gene from different tissues. Additionally, false-positive gene-trait pairs can arise due to correlations with the direct effects of genetic variants. In this study, we introduce TWASKnockoff, a new knockoff-based framework for detecting causal gene-tissue pairs using GWAS summary statistics and eQTL data. Unlike marginal testing in traditional TWAS methods, TWASKnockoff examines the conditional independence for each gene-trait pair, considering both correlations in cis-predicted expression across genes and correlations between gene expression levels and genetic variants. TWASKnockoff estimates the theoretical correlation matrix for all genetic elements (cis-predicted expression across genes and genotypes for genetic variants) by averaging estimations from parametric boot-strap samples and then performs knockoff-based inference to detect causal gene-trait pairs while controlling the false discovery rate (FDR). Through empirical simulations and an application to type 2 diabetes (T2D) data, we demonstrate that TWASKnockoff achieves superior FDR control and improves the average power in detecting causal gene-trait pairs at a fixed FDR level.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Joint Modeling of Effect Sizes for Two Correlated Traits: Characterizing Trait Properties to Enhance Polygenic Risk Prediction 98%
- Leveraging expression from multiple tissues using sparse canonical correlation analysis (sCCA) and aggregate tests improves the power of transcriptome-wide association studies (TWAS) 97%
- Identifying Causal Variants by Fine Mapping Across Multiple Studies 97%
Similar papers in this journal
- Analyzing and Reconciling Colocalization and Transcriptome-wide Association Studies from the Perspective of Inferential Reproducibility 97%
- Fast and Accurate Bayesian Polygenic Risk Modeling with Variational Inference 97%
- Sparse modeling of interactions enables fast detection of genome-wide epistasis in biobank-scale studies 97%
Similar papers in this journal
Similar papers in this journal
- Efficient gene-environment interaction tests for large biobank-scale sequencing studies 97%
- Assumptions about frequency-dependent architectures of complex traits bias measures of functional enrichment 96%
- Identity-by-descent mapping using multi-individual IBD with genome-wide multiple testing adjustment 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.