A Single-Cell-Resolution Quantitative Metric of Similarity to a Target Cell Type for scRNA-seq Data

Zuolin Cheng, Songtao Wei, Guoqiang Yu
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Abstract

Empowered by advances in single-cell RNA sequencing techniques (scRNA-seq), discovering new cell types or new subsets of a cell type has become an increasingly popular research interest. This type of study, by nature, requires assessment of similarity between cell groups. However, so far there is no quantitative metric for accurate and objective evaluation of such similarity; while current practice suffers from quite a few challenges including subjectivity. In this work, we propose a novel quantitative metric of single-cell-to-target-cell-type similarity, on the basis of scRNA-seq data and the signatures or differentially expressed gene (DEG) list of the target cell type. The proposed similarity score, TySim, evaluates the statistical significance of joint differential expression of the given DEGs in the cell to be tested. For this statistical test, the null distribution is established upon full consideration of complex factors causing heterogeneous sequencing efficiency of genes/cells. The design of TySim avoids the needs for clustering and for batch effect removal on cross-platform data, detouring the accompanying risks and burdens. Being the first quantitative metric of similarity to target cell type at a single-cell resolution, TySim has the potential to facilitate and enable a variety of biological studies. We validated the effectiveness of TySim and explored the possible directions of application through three example study cases of real datasets. Experimental results demonstrate TySim’s superior performance and great potential in making contributions to biological studies.
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scRNA-seq数据中与靶细胞类型相似性的单细胞分辨率定量度量
随着单细胞RNA测序技术(scRNA-seq)的进步,发现新的细胞类型或细胞类型的新亚群已成为越来越受欢迎的研究兴趣。从本质上讲,这种类型的研究需要评估细胞组之间的相似性。然而,到目前为止,还没有准确客观评价这种相似性的定量指标;而目前的实践面临着主观性等诸多挑战。在这项工作中,我们基于scRNA-seq数据和靶细胞类型的特征或差异表达基因(DEG)列表,提出了一种新的单细胞与靶细胞类型相似性的定量度量。所提出的相似度评分TySim评估待测细胞中给定deg联合差异表达的统计学意义。在此统计检验中,零分布的建立充分考虑了导致基因/细胞测序效率异质性的复杂因素。TySim的设计避免了对跨平台数据进行聚类和批处理效果去除的需要,规避了随之而来的风险和负担。作为第一个在单细胞分辨率下与靶细胞类型相似的定量指标,TySim具有促进和实现各种生物学研究的潜力。通过三个真实数据集的实例研究,验证了TySim的有效性,并探索了可能的应用方向。实验结果表明,TySim具有优异的性能,在生物学研究方面具有很大的潜力。
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