RIA:一种新的基于回归的单细胞RNA测序方法

Bang Tran, Duc Tran, Hung Nguyen, N. S. Vo, Tin Nguyen
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引用次数: 4

摘要

单细胞技术的进步使基因组学研究从分析大块组织转向对单个细胞的全面表征。这为基础生物学和临床研究提供了巨大的机会。因此,短寿命祖细胞、干细胞、癌症干细胞或循环肿瘤细胞的鉴定和表征对于更好地理解正常和病变组织生物学至关重要。然而,量化每个细胞中的基因表达仍然是一个重大挑战,因为单个细胞中可用的mRNA量很低。这将导致由退出事件引起的多余的零计数。在这里,我们介绍RIA,一种基于回归的方法,能够可靠地恢复单细胞数据中的缺失值,从而可以有效地提高下游分析的性能。我们使用5个scRNA-seq数据集(共3,535个细胞)将RIA与最先进的方法进行比较。在分析的每个数据集中,RIA在改善细胞群体识别同时保护生物景观方面优于现有方法。我们还证明,RIA能够推断胚胎发育阶段的时间轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RIA: a novel Regression-based Imputation Approach for single-cell RNA sequencing
Advances in single-cell technologies have shifted genomics research from the analysis of bulk tissues toward a comprehensive characterization of individual cells. This holds enormous opportunities for both basic biology and clinical research. As such, identification and characterization of shortlived progenitors, stem cells, cancer stem cells, or circulating tumor cells are essential to better understand both normal and diseased tissue biology. However, quantifying gene expression in each cell remains a significant challenge due to the low amount of mRNA available within individual cells. This leads to the excess amount of zero counts caused by dropout events. Here we introduce RIA, a regression-based approach, that is able to reliably recover the missing values in single-cell data and thus can effectively improve the performance of downstream analyses. We compare RIA with state-of-the-art methods using five scRNA-seq datasets with a total of 3,535 cells. In each dataset analyzed, RIA outperforms existing approaches in improving the identification of cell populations while preserving the biological landscape. We also demonstrate that RIA is able to infer temporal trajectories of embryonic development stages.
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