4.8 Article

Reconstruction of complex single-cell trajectories using CellRouter

期刊

NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-03214-y

关键词

-

资金

  1. US National Institute of Diabetes and Digestive and Kidney Diseases [R24DK092760, K08DK114527-01]
  2. National Institute of Allergy and Infectious Diseases [R37AI039394]
  3. National Heart, Lung, Blood Institute Progenitor Cell Biology Consortium [UO1-HL100001]
  4. Progenitor Cell Translation Consortium [UO1-HL134812]
  5. Doris Duke Medical Foundation
  6. St. Baldrick's Foundation
  7. Pedals for Pediatrics
  8. Wenner-Gren Foundation
  9. Howard Hughes Medical Institute

向作者/读者索取更多资源

A better understanding of the cell-fate transitions that occur in complex cellular ecosystems in normal development and disease could inform cell engineering efforts and lead to improved therapies. However, a major challenge is to simultaneously identify new cell states, and their transitions, to elucidate the gene expression dynamics governing cell-type diversification. Here, we present CellRouter, a multifaceted single-cell analysis platform that identifies complex cell-state transition trajectories by using flow networks to explore the subpopulation structure of multi-dimensional, single-cell omics data. We demonstrate its versatility by applying CellRouter to single-cell RNA sequencing data sets to reconstruct cell-state transition trajectories during hematopoietic stem and progenitor cell (HSPC) differentiation to the erythroid, myeloid and lymphoid lineages, as well as during re-specification of cell identity by cellular reprogramming of monocytes and B-cells to HSPCs. CellRouter opens previously undescribed paths for in-depth characterization of complex cellular ecosystems and establishment of enhanced cell engineering approaches.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据