| Literature DB >> 27883891 |
Justin Feigelman1, Stefan Ganscha2, Simon Hastreiter3, Michael Schwarzfischer4, Adam Filipczyk5, Timm Schroeder3, Fabian J Theis6, Carsten Marr7, Manfred Claassen8.
Abstract
Many cellular effectors of pluripotency are dynamically regulated. In principle, regulatory mechanisms can be inferred from single-cell observations of effector activity across time. However, rigorous inference techniques suitable for noisy, incomplete, and heterogeneous data are lacking. Here, we introduce stochastic inference on lineage trees (STILT), an algorithm capable of identifying stochastic models that accurately describe the quantitative behavior of cell fate markers observed using time-lapse microscopy data collected from proliferating cell populations. STILT performs exact Bayesian parameter inference and stochastic model selection using a particle-filter-based algorithm. We use STILT to investigate the autoregulation of Nanog, a heterogeneously expressed core pluripotency factor, in mouse embryonic stem cells. STILT rejects the possibility of positive Nanog autoregulation with high confidence; instead, model predictions indicate weak negative feedback. We use STILT for rational experimental design and validate model predictions using novel experimental data. STILT is available for download as an open source framework from http://www.imsb.ethz.ch/research/claassen/Software/stilt---stochastic-inference-on-lineage-trees.html. Copyright ÂEntities:
Keywords: Bayesian inference; autoregulation; lineage trees; model selection; mouse embryonic stem cells; nanog; parameter inference; particle filtering; state space inference; stochastic modeling
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Year: 2016 PMID: 27883891 DOI: 10.1016/j.cels.2016.11.001
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304