Author Summary | We introduce a new unobserved factor, which describes the pathway activity of single cells . |
Author Summary | We apply our model to gene silencing screens, investigating human rhino virus infection of single cells from microscopy imaging features. |
Discussion | A limitation of the current model formulation is the assumption of independent single cell observations. |
Discussion | Especially in the light of single cell data sets, which show large heterogeneity among individual observations, our approach is beneficial. |
Introduction | Such variation on the single cell level needs to be accounted for. |
Network inference under unknown pathway activity | Given single cell data D = (dekc) with c = 1, . |
Network inference under unknown pathway activity | In the following, we show improved network inference with NEMiX in simulations and then infer networks of high accuracy, from single cell gene silencing experiments. |
Simulation study | For the NEM approach we had to summarize the single cell observations to the gene level. |
The NEM framework | ., K}, With single cell observations c E {1, . |
The NEM framework | Regarding single cells as independent, for a given network structure (I), the local likelihoods further decompose into |
Discussion | Here, we present a mechanistic single cell growth model that is able to predict cell growth and division timing in budding yeast populations. |
Introduction | Our approach is to model single cells that are capable of growth and division, and grow them in in sil-ico cell cultures. |
Parameter estimation | We estimate five out of 14 parameters because to a certain degree we anticipated parameter correlations, over-fitting or under-determination of parameters since the nature of the data (population averaged) and the parameters ( single cell ) are distinct. |
Results | The volume trajectory for a single cell is biphasic With altered growth rates dependent on cell cycle stage as observed experimentally as well (Fig 1B) [15, 40—42]. |
Supporting Information | Single cell Model-2 in SBML format. |
The model | The model itself is a single cell model that can grow and divide (SI File). |
The model | To model entire asynchronously growing cell cultures, however, we developed an algorithm to simultaneously simulate a growing ensemble of the single cell models [32]. |
mCLB localization is required to equilibrate S-Gz-M duration between generations | Single cell data has shown in detail that there is little difference for time in S-GZ-M between daughters and mothers (Table 3) [14]. |
Discussion | Third, our method analyzes bulk populations of cells to identify changes in cell state ratios, rather than analyzing large numbers of single cells . |
Inhibition of RUNX1 Traps MCF10A Mammary Stem Cells in a Bipotent State | To directly examine this possibility we assessed Whether single cells from RUNXl inhibited spheres could form tissue rudiments When seeded into collagen. |
Inhibition of RUNX1 Traps MCF10A Mammary Stem Cells in a Bipotent State | We seeded cells With dox to form RUNXl inhibited spheres, harvested and dissociated the spheres by treatment With collagenase and trypsin, and then reseeded single cells into collagen With or Without dox. |