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首页> 外文期刊>BMC Bioinformatics >MCA: Multiresolution Correlation Analysis, a graphical tool for subpopulation identification in single-cell gene expression data
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MCA: Multiresolution Correlation Analysis, a graphical tool for subpopulation identification in single-cell gene expression data

机译:MCA:多分辨率相关分析,用于单细胞基因表达数据中亚群鉴定的图形工具

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Background Biological data often originate from samples containing mixtures of subpopulations, corresponding e.g. to distinct cellular phenotypes. However, identification of distinct subpopulations may be difficult if biological measurements yield distributions that are not easily separable. Results We present Multiresolution Correlation Analysis (MCA), a method for visually identifying subpopulations based on the local pairwise correlation between covariates, without needing to define an a priori interaction scale. We demonstrate that MCA facilitates the identification of differentially regulated subpopulations in simulated data from a small gene regulatory network, followed by application to previously published single-cell qPCR data from mouse embryonic stem cells. We show that MCA recovers previously identified subpopulations, provides additional insight into the underlying correlation structure, reveals potentially spurious compartmentalizations, and provides insight into novel subpopulations. Conclusions MCA is a useful method for the identification of subpopulations in low-dimensional expression data, as emerging from qPCR or FACS measurements. With MCA it is possible to investigate the robustness of covariate correlations with respect subpopulations, graphically identify outliers, and identify factors contributing to differential regulation between pairs of covariates. MCA thus provides a framework for investigation of expression correlations for genes of interests and biological hypothesis generation.
机译:背景生物数据通常来自含有亚群混合物的样品,例如到不同的细胞表型。但是,如果生物学测量结果产生的分布不容易分离,则很难区分不同的亚群。结果我们提出了多分辨率相关分析(MCA),这是一种基于协变量之间的局部成对相关性直观地识别亚种群的方法,而无需定义先验相互作用量表。我们证明,MCA有助于从一个小基因调节网络的模拟数据中识别差异调节的亚群,然后应用于小鼠胚胎干细胞中以前发布的单细胞qPCR数据。我们表明,MCA恢复了先前确定的亚群,提供了对潜在相关结构的更多洞察力,揭示了潜在的伪造区室化,并提供了对新型亚群的洞察力。结论MCA是鉴定qPCR或FACS测量中出现的低维表达数据中亚群的有用方法。使用MCA,有可能研究关于子种群的协变量相关性的鲁棒性,以图形方式识别异常值,并识别有助于协变量对之间差异调节的因素。因此,MCA提供了一个框架,可用于研究感兴趣基因的表达相关性和生物学假设的产生。

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