CellTracer: a comprehensive database to dissect the causative multilevel interplay contributing to cell development trajectories.
CellTracer: a comprehensive database to dissect the causative multilevel interplay contributing to cell development trajectories.
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CellTracer:一个综合数据库,用于剖析促成细胞发育轨迹的因果多级相互作用
DOI:
10.1093/nar/gkac892
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发表时间:
2023-01-06
影响因子:
14.9
通讯作者:
Li, Xia
中科院分区:
文献类型:
--
作者:
Guo, Qiuyan;Wang, Peng;Liu, Qian;Hao, Yangyang;Gao, Yue;Qi, Yue;Xu, Rongji;Chen, Hongyan;Xin, Mengyu;Wu, Xiaoting;Sun, Rui;Zhi, Hui;Zhang, Yunpeng;Ning, Shangwei;Li, Xia
Abstract During the complex process of tumour development, the unique destiny of cells is driven by the fine-tuning of multilevel features such as gene expression, network regulation and pathway activation. The dynamic formation of the tumour microenvironment influences the therapeutic response and clinical outcome. Thus, characterizing the developmental landscape and identifying driver features at multiple levels will help us understand the pathological development of disease in individual cell populations and further contribute to precision medicine. Here, we describe a database, CellTracer (http://bio-bigdata.hrbmu.edu.cn/CellTracer), which aims to dissect the causative multilevel interplay contributing to cell development trajectories. CellTracer consists of the gene expression profiles of 1 941 552 cells from 222 single-cell datasets and provides the development trajectories of different cell populations exhibiting diverse behaviours. By using CellTracer, users can explore the significant alterations in molecular events and causative multilevel crosstalk among genes, biological contexts, cell characteristics and clinical treatments along distinct cell development trajectories. CellTracer also provides 12 flexible tools to retrieve and analyse gene expression, cell cluster distribution, cell development trajectories, cell-state variations and their relationship under different conditions. Collectively, CellTracer will provide comprehensive insights for investigating the causative multilevel interplay contributing to cell development trajectories and serve as a foundational resource for biomarker discovery and therapeutic exploration within the tumour microenvironment.
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影响因子:
64.8
作者:
Cao, Junyue;Spielmann, Malte;Shendure, Jay
通讯作者:
Shendure, Jay
DOI:
10.1038/s41581-018-0021-7
发表时间:
2018-08
期刊:
Nature reviews. Nephrology
影响因子:
--
作者:
Potter SS
通讯作者:
Potter SS
影响因子:
14.9
作者:
The Gene Ontology Consortium
通讯作者:
The Gene Ontology Consortium
影响因子:
30.5
作者:
Avni, O;Lee, D;Rao, A
通讯作者:
Rao, A
影响因子:
64.8
作者:
Buenrostro JD;Wu B;Litzenburger UM;Ruff D;Gonzales ML;Snyder MP;Chang HY;Greenleaf WJ
通讯作者:
Greenleaf WJ