CellCall: integrating paired ligand-receptor and transcription factor activities for cell-cell communication.
CellCall: integrating paired ligand-receptor and transcription factor activities for cell-cell communication.
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CellCall:整合配对配体-受体和转录因子活性以进行细胞-细胞通讯
DOI:
10.1093/nar/gkab638
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发表时间:
2021-09-07
影响因子:
14.9
通讯作者:
Zhao X
中科院分区:
文献类型:
--
作者:
Zhang Y;Liu T;Hu X;Wang M;Wang J;Zou B;Tan P;Cui T;Dou Y;Ning L;Huang Y;Rao S;Wang D;Zhao X
Abstract With the dramatic development of single-cell RNA sequencing (scRNA-seq) technologies, the systematic decoding of cell-cell communication has received great research interest. To date, several in-silico methods have been developed, but most of them lack the ability to predict the communication pathways connecting the insides and outsides of cells. Here, we developed CellCall, a toolkit to infer inter- and intracellular communication pathways by integrating paired ligand-receptor and transcription factor (TF) activity. Moreover, CellCall uses an embedded pathway activity analysis method to identify the significantly activated pathways involved in intercellular crosstalk between certain cell types. Additionally, CellCall offers a rich suite of visualization options (Circos plot, Sankey plot, bubble plot, ridge plot, etc.) to present the analysis results. Case studies on scRNA-seq datasets of human testicular cells and the tumor immune microenvironment demonstrated the reliable and unique functionality of CellCall in intercellular communication analysis and internal TF activity exploration, which were further validated experimentally. Comparative analysis of CellCall and other tools indicated that CellCall was more accurate and offered more functions. In summary, CellCall provides a sophisticated and practical tool allowing researchers to decipher intercellular communication and related internal regulatory signals based on scRNA-seq data. CellCall is freely available at https://github.com/ShellyCoder/cellcall.
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影响因子:
4.6
作者:
Han H;Shim H;Shin D;Shim JE;Ko Y;Shin J;Kim H;Cho A;Kim E;Lee T;Kim H;Kim K;Yang S;Bae D;Yun A;Kim S;Kim CY;Cho HJ;Kang B;Shin S;Lee I
通讯作者:
Lee I
影响因子:
4.4
作者:
Bovolenta LA;Acencio ML;Lemke N
通讯作者:
Lemke N
影响因子:
14.9
作者:
Griffon A;Barbier Q;Dalino J;van Helden J;Spicuglia S;Ballester B
通讯作者:
Ballester B
影响因子:
48
作者:
Browaeys, Robin;Saelens, Wouter;Saeys, Yvan
通讯作者:
Saeys, Yvan
影响因子:
5.6
作者:
Handly LN;Yao J;Wollman R
通讯作者:
Wollman R