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GeneticsbioRxiv
Preprint

scPrediXcan integrates advances in deep learning and single-cell data into a powerful cell-type-specific transcriptome-wide association study framework

Yichao ZhouiD, Temidayo Adeluwa, Lisha ZhuiD, Sofia Salazar, Sarah SumneriD, Hyunki KimiD, Saideep GonaiD, Festus M. NyasimiiD, Rohit N. KulkarniiD, Joseph E. PowelliD, Ravi MadduriiD, Boxiang LiuiD, Mengjie CheniD, Hae Kyung ImiD

Abstract

Transcriptome-wide association studies (TWAS) help identify disease causing genes, but often fail to pinpoint disease mechanisms at the cellular level because of the limited sample sizes and sparsity of cell-type-specific expression data. Here we propose scPrediXcan which integrates state-of-the-art deep learning approaches that predict epigenetic features from DNA sequences with the canonical TWAS framework. Our prediction approach, ctPred, predicts cell-type-specific expression with high accuracy and captures complex gene regulatory grammar that linear models overlook. Applied to type 2 diabetes and systemic lupus erythematosus, scPrediXcan outperformed the canonical TWAS framework by identifying more candidate causal genes, explaining more genome-wide association studies (GWAS) loci, and providing insights into the cellular specificity of TWAS hits. Overall, our results demonstrate that scPrediXcan represents a significant advance, promising to deepen our understanding of the cellular mechanisms underlying complex diseases.

PDFDOI

02 /Specification & Classification

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