Concepts and limitations for learning developmental trajectories from single cell genomics

Tritschler S, Buettner M, Fischer DS, Lange M, Bergen V, Lickert H, Theis FJ (2019)


Publication Type: Journal article, Review article

Publication year: 2019

Journal

Book Volume: 146

Article Number: dev170506

Journal Issue: 12

DOI: 10.1242/dev.170506

Abstract

Single cell genomics has become a popular approach to uncover the cellular heterogeneity of progenitor and terminally differentiated cell types with great precision. This approach can also delineate lineage hierarchies and identify molecular programmes of cell-fate acquisition and segregation. Nowadays, tens of thousands of cells are routinely sequenced in single cell-based methods and even more are expected to be analysed in the future.However, interpretation of the resulting data is challenging and requires computational models at multiple levels of abstraction. In contrast to other applications of single cell sequencing, where clustering approaches dominate, developmental systems are generally modelled using continuous structures, trajectories and trees. These trajectory models carry the promise of elucidating mechanisms of development, disease and stimulation response at very high molecular resolution. However, their reliable analysis and biological interpretation requires an understanding of their underlying assumptions and limitations. Here, we review the basic concepts of such computational approaches and discuss the characteristics of developmental processes that can be learnt from trajectory models.

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How to cite

APA:

Tritschler, S., Buettner, M., Fischer, D.S., Lange, M., Bergen, V., Lickert, H., & Theis, F.J. (2019). Concepts and limitations for learning developmental trajectories from single cell genomics. Development, 146(12). https://doi.org/10.1242/dev.170506

MLA:

Tritschler, Sophie, et al. "Concepts and limitations for learning developmental trajectories from single cell genomics." Development 146.12 (2019).

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