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Truncated Robust Principal Component Analysis and Noise Reduction for Single Cell RNA-seq Data

机译:单细胞RNA-seq数据的截断鲁棒主成分分析和降噪

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The development of single cell RNA sequencing (scRNA-seq) has enabled innovative approaches to investigating mRNA abundances. In our study, we are interested in extracting the systematic patterns of scRNA-seq data in an unsupervised manner, thus we have developed two extensions of robust principal component analysis (RPCA). First, we present a truncated version of RPCA (tRPCA), that is much faster and memory efficient. Second, we introduce a noise reduction in tRPCA with L_2 regularization (tRPCAL2). Unlike RPCA that only considers a low-rank L and sparse S matrices, the proposed method can also extract a noise E matrix inherent in modern genomic data. We demonstrate its usefulness by applying our methods on the peripheral blood mononuclear cell (PBMC) scRNA-seq data. Particularly, the clustering of a low-rank L matrix showcases better classification of unlabeled single cells. Overall, the proposed variants are well-suited for high-dimensional and noisy data that are routinely generated in genomics.
机译:单细胞RNA测序(scRNA-seq)的发展为研究mRNA丰度提供了创新的方法。在我们的研究中,我们有兴趣以无监督的方式提取scRNA-seq数据的系统模式,因此我们开发了鲁棒主成分分析(RPCA)的两个扩展。首先,我们提出了RPCA(tRPCA)的截短版本,该版本速度更快且内存效率更高。其次,我们在具有L_2正则化(tRPCAL2)的tRPCA中引入了降噪功能。与仅考虑低秩L和稀疏S矩阵的RPCA不同,所提出的方法还可以提取现代基因组数据中固有的噪声E矩阵。我们通过将我们的方法应用于外周血单核细胞(PBMC)scRNA-seq数据来证明其有用性。特别是,低秩L矩阵的聚类展示了未标记单细胞的更好分类。总体而言,提出的变体非常适合基因组学中常规生成的高维和嘈杂数据。

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