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scPrediXcan将深度学习和单细胞数据方面的进展整合到一个强大的细胞类型特异性全转录组关联研究框架中。

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

作者信息

Zhou Yichao, Adeluwa Temidayo, Zhu Lisha, Salazar-Magaña Sofia, Sumner Sarah, Kim Hyunki, Gona Saideep, Nyasimi Festus, Kulkarni Rohit, Powell Joseph, Madduri Ravi, Liu Boxiang, Chen Mengjie, Im Hae Kyung

机构信息

Committee of Genetic, Genomics, and Systems Biology, University of Chicago, Chicago, Illinois, United States of America.

Department of Medicine, Section of Genetic Medicine, University of Chicago, Chicago, Illinois, United States of America.

出版信息

bioRxiv. 2025 Mar 4:2024.11.11.623049. doi: 10.1101/2024.11.11.623049.

DOI:10.1101/2024.11.11.623049
PMID:39605417
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11601274/
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.

摘要

全转录组关联研究(TWAS)有助于识别致病基因,但由于样本量有限以及细胞类型特异性表达数据的稀疏性,往往无法在细胞水平上精确确定疾病机制。在此,我们提出了scPrediXcan,它将从DNA序列预测表观遗传特征的先进深度学习方法与经典的TWAS框架相结合。我们的预测方法ctPred能够高精度地预测细胞类型特异性表达,并捕捉线性模型忽略的复杂基因调控语法。应用于2型糖尿病和系统性红斑狼疮时,scPrediXcan通过识别更多候选因果基因、解释更多全基因组关联研究(GWAS)位点以及深入了解TWAS命中的细胞特异性,优于经典的TWAS框架。总体而言,我们的结果表明scPrediXcan代表了一项重大进展,有望加深我们对复杂疾病潜在细胞机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/a6e33269d183/nihpp-2024.11.11.623049v2-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/db49c3354163/nihpp-2024.11.11.623049v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/fd4be3c7527b/nihpp-2024.11.11.623049v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/6838405f93a1/nihpp-2024.11.11.623049v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/628f7971fb14/nihpp-2024.11.11.623049v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/884e8a7c1b17/nihpp-2024.11.11.623049v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/a6e33269d183/nihpp-2024.11.11.623049v2-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/db49c3354163/nihpp-2024.11.11.623049v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/fd4be3c7527b/nihpp-2024.11.11.623049v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/6838405f93a1/nihpp-2024.11.11.623049v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/628f7971fb14/nihpp-2024.11.11.623049v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/884e8a7c1b17/nihpp-2024.11.11.623049v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a8/11956650/a6e33269d183/nihpp-2024.11.11.623049v2-f0008.jpg

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本文引用的文献

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Personal transcriptome variation is poorly explained by current genomic deep learning models.当前的基因组深度学习模型对个体转录组变异的解释能力较差。
Nat Genet. 2023 Dec;55(12):2056-2059. doi: 10.1038/s41588-023-01574-w. Epub 2023 Nov 30.
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Benchmarking of deep neural networks for predicting personal gene expression from DNA sequence highlights shortcomings.用于从DNA序列预测个人基因表达的深度神经网络基准测试凸显了不足之处。
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Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases.
利用基因特征的多基因富集来预测复杂性状和疾病的潜在基因。
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The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits.2 型糖尿病知识库:一个开放获取的遗传资源库,专门用于 2 型糖尿病和相关特征。
Cell Metab. 2023 Apr 4;35(4):695-710.e6. doi: 10.1016/j.cmet.2023.03.001. Epub 2023 Mar 23.
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A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk.全基因组 CRISPR 筛选鉴定 CALCOCO2 为调节β细胞功能的因子,影响 2 型糖尿病风险。
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3D chromatin maps of the human pancreas reveal lineage-specific regulatory architecture of T2D risk.人类胰腺的 3D 染色质图谱揭示了 T2D 风险的谱系特异性调控结构。
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Single-cell RNA-sequencing of peripheral blood mononuclear cells reveals widespread, context-specific gene expression regulation upon pathogenic exposure.外周血单核细胞的单细胞 RNA 测序揭示了在致病暴露时广泛存在的、特定于上下文的基因表达调控。
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