2022
DOI: 10.1016/j.bpj.2022.07.014
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A data-assimilation approach to predict population dynamics during epithelial-mesenchymal transition

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Cited by 3 publications
(3 citation statements)
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“…The resulting optimal trajectories for the time-dependent and dose-dependent data with confidence intervals are shown in Figures 5 B and 5F respectively. Although our 45-gene approach exhibited some differences between the predicted and simulated phenotypic fractions as a function of dose reported by previous studies, our overall trends were in general agreement 56 ( Figure 5 F). From the steady state fractions obtained from the dose-dependent data, it is evident that the distribution of fractions for the flow cytometry data at day 18 resembles the equilibrium state fractions closely (roughly 113.6 pM, see supplemental information for dimensionality analysis).…”
Section: Resultssupporting
confidence: 83%
“…The resulting optimal trajectories for the time-dependent and dose-dependent data with confidence intervals are shown in Figures 5 B and 5F respectively. Although our 45-gene approach exhibited some differences between the predicted and simulated phenotypic fractions as a function of dose reported by previous studies, our overall trends were in general agreement 56 ( Figure 5 F). From the steady state fractions obtained from the dose-dependent data, it is evident that the distribution of fractions for the flow cytometry data at day 18 resembles the equilibrium state fractions closely (roughly 113.6 pM, see supplemental information for dimensionality analysis).…”
Section: Resultssupporting
confidence: 83%
“…The resulting optimal trajectories for the time-dependent and dose-dependent data with confidence intervals are shown in Figure 5B and 5F respectively. Although our 45-gene approach exhibited some differences between the predicted and simulated phenotypic fractions as a function of dose reported by previous studies, our overall trends were in general agreement 35 (Figure 5F). From the steady state fractions obtained from the dose-dependent data, it is evident that the distribution of fractions for the flow cytometry data at day 18 oesemoles the equilibrium state fractions closely (roughly 113.6 pM, see Supplementary Information for dimensionality analysis).…”
Section: Resultssupporting
confidence: 83%
“…The resulting optimal trajectories for the time-dependent and dose-dependent data with confidence intervals are shown in Figures 5B and 5F respectively. Although our 45-gene approach exhibited some differences between the predicted and simulated phenotypic fractions as a function of dose reported by previous studies, our overall trends were in general agreement 56 (Figure 5F). From the steady state fractions obtained from the dose-dependent data, it is evident that the distribution of fractions for the flow cytometry data at day 18 resembles the equilibrium state fractions closely (roughly 113.6 pM, see supplemental information for dimensionality analysis).…”
Section: Ll Open Accesssupporting
confidence: 83%