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Studying the progression of the proliferative and differentiative patterns of neural stem cells at the individual cell level is crucial to the understanding of cortex development and how the disruption of such patterns can lead to malformations and neurodevelopmental diseases. However, our understanding of the precise lineage progression programme at single-cell resolution is still incomplete due to the technical variations in lineage-tracing approaches. One of the key challenges involves developing a robust theoretical framework in which we can integrate experimental observations and introduce correction factors to obtain a reliable and representative description of the temporal modulation of proliferation and differentiation. In order to obtain more conclusive insights, we carry out virtual clonal analysis using mathematical modelling and compare our results against experimental data. Using a dataset obtained with Mosaic Analysis with Double Markers, we illustrate how the theoretical description can be exploited to interpret and reconcile the disparity between virtual and experimental results.

Original publication

DOI

10.1111/joa.13001

Type

Journal article

Journal

J Anat

Publication Date

09/2019

Volume

235

Pages

687 - 696

Keywords

Mosaic Analysis with Double Markers, birth-death stochastic process, branching processes, clonal analysis, cortical neurogenesis, Animals, Cell Lineage, Cerebral Cortex, Clone Cells, Mice, Models, Biological, Neurogenesis