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Identifying Differentially Expressed Genes of Zero Inflated Single Cell RNA Sequencing Data Using Mixed Model Score Tests

机译:使用混合模型评分测试识别零充气单细胞RNA测序数据的差异表达基因

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Single cell RNA sequencing (scRNA-seq) allows quantitative measurement and comparison of gene expression at the resolution of single cells. Ignoring the batch effects and zero inflation of scRNA-seq data, many proposed differentially expressed (DE) methods might generate bias. We propose a method, single cell mixed model score tests (scMMSTs), to efficiently identify DE genes of scRNA-seq data with batch effects using the generalized linear mixed model (GLMM). scMMSTs treat the batch effect as a random effect. For zero inflation, scMMSTs use a weighting strategy to calculate observational weights for counts independently under zero-inflated and zero-truncated distributions. Counts data with calculated weights were subsequently analyzed using weighted GLMMs. The theoretical null distributions of the score statistics were constructed by mixed Chi-square distributions. Intensive simulations and two real datasets were used to compare edgeR-zinbwave, DESeq2-zinbwave, and scMMSTs. Our study demonstrates that scMMSTs, as supplement to standard methods, are advantageous to define DE genes of zero-inflated scRNA-seq data with batch effects.
机译:单细胞RNA测序(ScRNA-SEQ)允许定量测量和比较单细胞分辨率的基因表达。忽略ScrNA-SEQ数据的批量效应和零充气,许多提出的差异表达(DE)方法可能会产生偏差。我们提出了一种方法,单细胞混合模型评分试验(SCMMSTS),以使用广义线性混合模型(GLMM)有效地用批量效应识别SCRNA-SEQ数据的DE基因。 SCMMSTS将批量效应视为随机效应。对于零充气,SCMMSTS使用加权策略在零充气和零截断的分布下独立地计算观测权重。随后使用加权GLMMS分析具有计算权重的数据。分数统计的理论为空分布由混合Chi-Square分布构成。密集的模拟和两个真实数据集用于比较Edger-Zinbwave,Deseq2-ZinbWave和SCMMSTS。我们的研究表明,作为标准方法的补充,SCMMSTS是有利的,是利用批量效应定义零充气瘢痕基-SEQ数据的DE基因。

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