2023
DOI: 10.1038/s41467-023-40503-7
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Cell-type-specific co-expression inference from single cell RNA-sequencing data

Abstract: The advancement of single cell RNA-sequencing (scRNA-seq) technology has enabled the direct inference of co-expressions in specific cell types, facilitating our understanding of cell-type-specific biological functions. For this task, the high sequencing depth variations and measurement errors in scRNA-seq data present two significant challenges, and they have not been adequately addressed by existing methods. We propose a statistical approach, CS-CORE, for estimating and testing cell-type-specific co-expressio… Show more

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Cited by 17 publications
(7 citation statements)
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“…The challenge in this task stems from the Granger causal relationship or time-dependent correlation [109]. A GCN can be used to analyze genes with similar functions or uncover the characteristics of genes in some diseases [110]. GCN and GRN are two different tasks because correlation does not imply causal relation [111].…”
Section: Explanations Of Scevalmentioning
confidence: 99%
“…The challenge in this task stems from the Granger causal relationship or time-dependent correlation [109]. A GCN can be used to analyze genes with similar functions or uncover the characteristics of genes in some diseases [110]. GCN and GRN are two different tasks because correlation does not imply causal relation [111].…”
Section: Explanations Of Scevalmentioning
confidence: 99%
“…The accurate identification and comprehensive study of these cells necessitate sequencing more cells. Beyond elucidating the nuances of DE analysis, our results imply the impacts on other analytical methodologies, including cell classification 22 , eQTL mapping 23 , and the construction of co-expression networks 24 . For example, in a fetal brain study, a reduction in the number of cells sequenced has resulted in diminished accuracy in cell type classification 25 .…”
Section: Discussionmentioning
confidence: 93%
“…Then, the data matrix is log-transformed (scanpy.pp.log1p). In the end, we selected the top 1000 genes ( 20 22 ) by the ranking variances of all samples (scanpy.pp.highly_variable_genes), which was performed variance calculation in Scanpy. More specifically, a normalized variance for each gene is computed.…”
Section: Methodsmentioning
confidence: 99%