Application to real outbreaks | Our estimate of R for MERS-CoV was 0.73 (0.54—0.96), whereas in a single-type branching process model R = 0.63 (0.49—0.85). |
Discussion | Using a multi-type branching process , we developed an inference framework to make better use of age-structured outbreak size data. |
Discussion | In a single-type branching process framework, the threshold is a single number: the total size of the outbreak [31, 16]. |
Estimating transmissibility and pre-existing immunity | We simulated outbreaks using a multi-type branching process with two groups, then used the outbreak size distribution to infer R0 and relative immunity in older individuals. |
Estimating transmissibility and pre-existing immunity | We compared these values with estimates from an inference framework based on a single-type branching process [15, 16, 17, 18]. |
Estimating transmissibility and pre-existing immunity | This bias is the result of our assumption that introductions occur randomly across the susceptible population, and illustrates an important caveat to inference of R from the mean outbreak size in a single-type branching process model. |
Introduction | However, existing techniques for estimating transmission potential from outbreak size data generally represent transmission in the host population using single-type branching process [15, 16, 17, 18]. |
Introduction | We made use of this observation by developing a novel age-structured model of stuttering transmission chains, which combined reported social contact data with a multi-type branching process [23, 24]. |
Offspring distribution | We used a multi-type branching process to model secondary infections (see Text 81 for details). |
Supporting Information | Estimates of R0 and relative susceptibility, S, when simulation model is a multi-type branching process with 15 age groups. |
Estimates from the parametric data analysis | Text, it follows that the 8* cell dynamics reduce to a subcritical branching process, |
Model | Mathematically, these dynamics are summarized as a two-type branching process , see also Fig. |
Model | Since the 8 cells in (1) undergo a critical branching process , their progeny will eventually go extinct (see also the discussion of 8*< cells below). |
Model | From this it is easy to see that the dynamics of the 8* cell population in the basal layer are governed by the continuous-time critical branching process |
Space and the impact of clustering | The subcritical branching process model above was derived under the assumption of a well-mixed basal layer where infected cells are surrounded primarily by susceptible cells. |
Space and the impact of clustering | Immune capacity in the branching process model. |
V | First, time to clearance is generally longer in the branching process model: the three dotted horizontal lines correspond to the three quartiles for the (M/fi_ = 1)distribution in Fig. |
V | Only for the (,u/fi_ = 8) -distri-bution, which corresponds to an 8-fold increase in immune capacity, are all three quartiles of the spatial model below the corresponding quartiles of the branching process model. |
V | This is due to the fact that, in contrast to the branching process model, elimination of an infected cell can trigger division of an 8* cell (with probability 195* > 0), therefore compensating for the loss of the infected cell and delaying clearance. |
Abstract | To study the joint effect of drug heterogeneity, growth rate, and evolution of resistance, we analyze a multi-type stochastic branching process describing growth of cancer cells in multiple compartments with different drug concentrations and limited migration between compartments. |
Generating function approach | The backward equations for this branching process are (see 81 Text for how to derive them) |
Results | Nevertheless, using the multiplicative properties of branching processes , we can calculate the probability of escape and the (conditional) average time to resistance for any given initial conditions of tumor size or metastases (see derivation details in 81 Text). |
Results | In this way, the two competing pathways can be seen as three-type branching processes , respectively, with different fitness |
Results | Since we are considering a branching process , larger population size is more likely to generate resistant mutation. |