scholarly journals Exploration of cell development pathways through high dimensional single cell analysis in trajectory space

2018 ◽  
Author(s):  
Denis Dermadi ◽  
Michael Bscheider ◽  
Kristina Bjegovic ◽  
Nicole H. Lazarus ◽  
Agata Szade ◽  
...  

High-dimensional single cell profiling coupled with computational modeling is emerging as a powerful means to elucidate developmental sequences and define genetic programs directing cell lineages. Here we introduce tSpace, an algorithm based on the concept of “trajectory space”, in which cells are defined by their distance along nearest neighbor pathways to every other cell in a population. tSpace outputs a dense matrix of cell-to-cell distances that quantitatively reflect the extent of phenotypic change along developmental paths (developmental distances). Graphical mapping of cells in trajectory space allows unsupervised reconstruction and straightforward exploration of complex developmental sequences. tSpace is robust, scalable, and implements a global approach that attempts to preserve both local and distant relationships in developmental pathways. Applied to high dimensional flow and mass cytometry data, the method faithfully reconstructs known pathways of thymic T cell development and provides novel insights into regulation of tonsillar B cell development and trafficking. Applied to single cell transcriptomic data, the method unfolds complex developmental sequences, recapitulates pathways leading from intestinal stem cells to specialized epithelial phenotypes more faithfully than existing algorithms, and reveals genetic programs that correlate with fate decisions. tSpace profiling of complex populations in high-dimensional trajectory space is well suited for hypothesis generation in developing cell systems.


iScience ◽  
2020 ◽  
Vol 23 (2) ◽  
pp. 100842 ◽  
Author(s):  
Denis Dermadi ◽  
Michael Bscheider ◽  
Kristina Bjegovic ◽  
Nicole H. Lazarus ◽  
Agata Szade ◽  
...  


2020 ◽  
Vol 11 (7) ◽  
Author(s):  
Qinglin Fei ◽  
Yu Pan ◽  
Wenji Lin ◽  
Yuanyuan Zhou ◽  
Xingxing Yu ◽  
...  


2018 ◽  
Vol 24 (2) ◽  
pp. 144-153 ◽  
Author(s):  
Carsten Krieg ◽  
Malgorzata Nowicka ◽  
Silvia Guglietta ◽  
Sabrina Schindler ◽  
Felix J Hartmann ◽  
...  


2021 ◽  
Author(s):  
Ke-Yue Ma ◽  
Alexandra A. Schonnesen ◽  
Chenfeng He ◽  
Amanda Y. Xia ◽  
Eric Sun ◽  
...  


2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Eric Czech ◽  
Bulent Arman Aksoy ◽  
Pinar Aksoy ◽  
Jeff Hammerbacher


2017 ◽  
Vol 118 (1) ◽  
Author(s):  
Tess Melinda Brodie ◽  
Vinko Tosevski


2019 ◽  
Vol 49 (2) ◽  
pp. 212-220 ◽  
Author(s):  
Edoardo Galli ◽  
Ekaterina Friebel ◽  
Florian Ingelfinger ◽  
Susanne Unger ◽  
Nicolás Gonzalo Núñez ◽  
...  


2016 ◽  
Author(s):  
Caleb Weinreb ◽  
Samuel Wolock ◽  
Allon Klein

MotivationSingle-cell gene expression profiling technologies can map the cell states in a tissue or organism. As these technologies become more common, there is a need for computational tools to explore the data they produce. In particular, existing data visualization approaches are imperfect for studying continuous gene expression topologies.ResultsForce-directed layouts of k-nearest-neighbor graphs can visualize continuous gene expression topologies in a manner that preserves high-dimensional relationships and allows manually exploration of different stable two-dimensional representations of the same data. We implemented an interactive web-tool to visualize single-cell data using force-directed graph layouts, called SPRING. SPRING reveals more detailed biological relationships than existing approaches when applied to branching gene expression trajectories from hematopoietic progenitor cells. Visualizations from SPRING are also more reproducible than those of stochastic visualization methods such as tSNE, a state-of-the-art tool.Availabilityhttps://kleintools.hms.harvard.edu/tools/spring.html,https://github.com/AllonKleinLab/SPRING/[email protected], [email protected]



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