Wishbone identifies bifurcating developmental trajectories from single-cell data

被引:410
作者
Setty, Manu [1 ]
Tadmor, Michelle D. [1 ]
Reich-Zeliger, Shlomit [2 ]
Ange, Omer [3 ]
Salame, Tomer Meir [4 ]
Kathail, Pooja [1 ]
Choi, Kristy [1 ]
Bendall, Sean [5 ]
Friedman, Nir [2 ]
Pe'er, Dana [1 ]
机构
[1] Columbia Univ, Dept Syst Biol, Dept Biol Sci, New York, NY USA
[2] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[3] Univ British Columbia, Dept Math, Vancouver, BC, Canada
[4] Weizmann Inst Sci, Biol Serv Unit, IL-76100 Rehovot, Israel
[5] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
GENE-EXPRESSION; TRANSCRIPTION FACTORS; DIFFUSION MAPS; RNA-SEQ; DIFFERENTIATION; TRANSFORMATION; HETEROGENEITY; MECHANISMS; LANDSCAPE; NETWORKS;
D O I
10.1038/nbt.3569
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Recent single-cell analysis technologies offer an unprecedented opportunity to elucidate developmental pathways. Here we present Wishbone, an algorithm for positioning single cells along bifurcating developmental trajectories with high resolution. Wishbone uses multi-dimensional single-cell data, such as mass cytometry or RNA-Seq data, as input and orders cells according to their developmental progression, and it pinpoints bifurcation points by labeling each cell as pre-bifurcation or as one of two post-bifurcation cell fates. Using 30-channel mass cytometry data, we show that Wishbone accurately recovers the known stages of T-cell development in the mouse thymus, including the bifurcation point. We also apply the algorithm to mouse myeloid differentiation and demonstrate its generalization to additional lineages. A comparison of Wishbone to diffusion maps, SCUBA and Monocle shows that it outperforms these methods both in the accuracy of ordering cells and in the correct identification of branch points.
引用
收藏
页码:637 / 645
页数:9
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