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A clustering-independent method for finding differentially expressed genes in single-cell transcriptome data

机译:用于在单细胞转录组数据中查找差异表达基因的聚类无关方法

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A common analysis of single-cell sequencing data includes clustering of cells and identifying differentially expressed genes (DEGs). How cell clusters are defined has important consequences for downstream analyses and the interpretation of results, but is often not straightforward. To address this difficulty, we present singleCellHaystack, a method that enables the prediction of DEGs without relying on explicit clustering of cells. Our method uses Kullback-Leibler divergence to find genes that are expressed in subsets of cells that are non-randomly positioned in a multidimensional space. Comparisons with existing DEG prediction approaches on artificial datasets show that singleCellHaystack has higher accuracy. We illustrate the usage of singleCellHaystack through applications on 136 real transcriptome datasets and a spatial transcriptomics dataset. We demonstrate that our method is a fast and accurate approach for DEG prediction in single-cell data. singleCellHaystack is implemented as an R package and is available from CRAN and GitHub.
机译:对单细胞测序数据的常见分析包括细胞聚类并鉴定差异表达基因(DEGS)。如何定义细胞集群对下游分析以及结果的解释具有重要影响,但往往并不简单。为了解决这个困难,我们呈现SingleCellhaystack,这是一种能够预测DEG的方法,而无需依赖于细胞的显式聚类。我们的方法使用Kullback-Leibler发散来查找以在多维空间中非随机定位的细胞亚群中表达的基因。人工数据集现有DEG预测方法的比较表明,SingleCellhaystack具有更高的准确性。我们说明了在136实际转录组数据集和空间转录组数据集上的应用程序使用SingleCellhaystack。我们展示了我们的方法是单细胞数据中的一种快速准确的DEG预测方法。 SingleCellhaystack被实现为R包,可从Cran和GitHub获得。

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