挖掘单细胞数据的细胞类型-疾病关联。

IF 4 Q1 GENETICS & HEREDITY NAR Genomics and Bioinformatics Pub Date : 2024-12-18 eCollection Date: 2024-12-01 DOI:10.1093/nargab/lqae180
Kevin G Chen, Kathryn O Farley, Timo Lassmann
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引用次数: 0

摘要

对潜在疾病的细胞机制的深入了解为有效设计药物和其他干预措施奠定了基础。现有的丰富的单细胞图谱为揭示不同细胞类型和时间点的表达模式的高分辨率信息提供了机会。为了更好地理解细胞类型和疾病之间的关联,我们利用先前开发的工具构建了一个标准化的分析管道,并系统地探索了四个单细胞数据集之间的关联,涵盖了一系列组织类型、细胞类型和发育时间段。我们利用一组现有的工具来鉴定每种细胞类型的共表达模块和时间模式,然后研究这些模块对已知疾病和表型的富集。我们的管道揭示了所有研究数据集中已知和新的假定细胞类型与疾病的关联。此外,我们发现自动发现的基因共表达模块和时间簇对于药物靶点来说是丰富的,这表明我们的分析可以用于识别新的治疗靶点。
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Mining single-cell data for cell type-disease associations.

A robust understanding of the cellular mechanisms underlying diseases sets the foundation for the effective design of drugs and other interventions. The wealth of existing single-cell atlases offers the opportunity to uncover high-resolution information on expression patterns across various cell types and time points. To better understand the associations between cell types and diseases, we leveraged previously developed tools to construct a standardized analysis pipeline and systematically explored associations across four single-cell datasets, spanning a range of tissue types, cell types and developmental time periods. We utilized a set of existing tools to identify co-expression modules and temporal patterns per cell type and then investigated these modules for known disease and phenotype enrichments. Our pipeline reveals known and novel putative cell type-disease associations across all investigated datasets. In addition, we found that automatically discovered gene co-expression modules and temporal clusters are enriched for drug targets, suggesting that our analysis could be used to identify novel therapeutic targets.

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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
95
审稿时长
15 weeks
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