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The term p(x t, a t, o t |z1 t-1) is the prior pdf that predicts the evolution of {x t, a t, o t } between consecutive time steps using the joint posterior pdf at the previous time step p xt-1, at-1, ot-1|z1:t-1) p xt-1t, a t, o t | z 1 : t - 1 ) = ∫ ∑ a t - 1 ∑ ot-1|z1 t-1 ot-1|z1 t-1 t | z 1 : t - 1, x t - 1, a t - 1, o t - 1 ).
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The interval "N" between two consecutive time steps can be calculated: N = T2-T1.
Notice that this model allows for arbitrary changes between two consecutive time steps, with the possible creation and/or deletion of any number of vertices and edges.
The movement of the parasite is measured by the pixel difference between two consecutive time steps: large changes in parasite shape or position lead to large difference value.
Size descriptors measure the size of a parasite by the total number of pixels of the body of the parasite and the area change of the parasite between two consecutive time steps.
To model the first assumption of asynchronous models, which states only one gene can be updated between two consecutive time steps, we use the following relation: (5) Equation (5) states that gene i in the next time step, takes the value as defined by the function x i (t+1) in Equation (1) and all the other genes stay at their current expression levels.
Once the process converged (L2-distance between probability vectors in consecutive time steps <10−6), a prediction was made for all genes in relevant intervals with visitation probability greater than θ.
This approach employs a quasi-steady model including equations of steady-state heat transfer for consecutive time steps of computation.
However, each fault is injected under the single-fault model and multiple faults exist only in consecutive time steps.
Consecutive time-steps of evolution are simulated by generating random numbers to decide which individuals recover or continue as infectives.
Notice that ICF was originally designed to be applied with multiple consensus steps between two consecutive time instants.
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