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1  genomic ancestry inference as a pooled semi-Markov process.
2 ty that reflects the strength of mixing in a Markov process.
3 nce) was analyzed with a computer model of a Markov process.
4 substitution is modeled by a continuous-time Markov process.
5 imilar to those of SCORE2 participants and a Markov process.
6 m with an exact and efficient non-reversible Markov process.
7 inferring parameters of a partially observed Markov process.
8  occurs in the study of large deviations for Markov processes.
9  the associated discrete-time discrete-space Markov processes.
10 the single-step dependency characteristic of Markov processes.
11 d in statistical mechanics and the theory of Markov processes.
12 cule time-binned FRET trajectories as hidden Markov processes, allowing one to determine, based on pr
13 s within blocks follows a time-inhomogeneous Markov process along the chromosome, and we choose among
14 sociation in a candidate region via a hidden Markov process and allow for correlation between linked
15 esent organelle inheritance as a first-order Markov process and describe two figures of merit based o
16              We quantify the phenomenon as a Markov process and discover that if the network fails to
17                     Our model of pooled semi-Markov process and inference algorithms may be of indepe
18 volution as a discrete space continuous time Markov process and introduce a neighbor-dependent model
19 on the description of protein evolution by a Markov process and the corresponding matrix of instantan
20 h is applicable to any system described by a Markov process and, owing to the analytic nature of the
21 neral mathematical framework for pooled semi-Markov processes and construct efficient inference algor
22 hod accurately infers parameters of the semi-Markov processes and parents' genomic ancestries.
23 the harmonic fields can be induced by simple Markov processes and that the corresponding stochastic d
24 P models latent phenotype states as a binary Markov process, and it employs an adaptive weighting str
25  linear framework, a graph-based approach to Markov processes, and show that it can accommodate many
26 multistate life tables under a discrete-time Markov process assumption.
27 ons: First, we show how it can be applied to Markov processes biased by arbitrary reweighting factors
28 g the memoryless property, consistent with a Markov process, but it overestimates the probability of
29 the gene tree and treats the coalescent as a Markov process describing the decay in the number of anc
30     We formulate a bivariate continuous-time Markov process for the numbers of T cells belonging to t
31 the channel is well described as a two-state Markov process, in which both the on- and off-rates are
32                In the algorithm a continuous Markov process is discretized as a jump process and the
33                 Tools from the theory of non-Markov processes may help us understand these memories b
34  of any input-output response arising from a Markov process model at thermodynamic equilibrium.
35                                            A Markov process model is used for nucleotide substitution
36 opose multipoint methods that are based on a Markov-process model of allele sharing along the chromos
37  to perform likelihood calculations based on Markov process models of nucleotide substitution allied
38                             In most cases, a Markov process of at least fourth-order was required to
39 lly relevant examples that at least for semi-Markov processes of first and second order, waiting-time
40  coarse graining that reduces the model to a Markov process on a finite number of "information states
41     The underlying model takes the form of a Markov process on an infinite dimensional state space.
42 ection [1], [2], in which the evolution of a Markov process on the graph is used as a zooming lens ov
43  We develop a theory of rattling in terms of Markov processes that gives simple and precise answers t
44 apshot time series data as a low-dimensional Markov process, thereby enabling an interpretable dynami
45 We constructed a decision analysis using the Markov process to model expected clinical outcomes and c
46 scillations, and it is demonstrated that for Markov processes to have oscillatory transients, its tra
47 fluorophore as an unobserved continuous time Markov process transitioning between a single fluorescen
48 ing the dynamics between helical states as a Markov process using a recently developed formalism.
49 tances are estimated by constructing spatial Markov processes using the information from both approxi
50                                            A Markov process was constructed to project the natural hi
51    Using the theory of linear elasticity and Markov processes, we simulate a model, which reproduces
52 how that 3D cancer cell motility is a hidden Markov process whereby the step size distributions of ce
53 The model is formulated as a continuous time Markov process, which is decomposed into a deterministic
54  show that the probability p(t) that a Gauss-Markov process will first exceed the boundary at time t
55 titution model based on a general reversible Markov process with a gamma distribution to account for
56 lution for each of the eight categories is a Markov process with discrete states in continuous time,
57 n described as an aggregated continuous-time Markov process with discrete states.
58 l the community's confidence in a claim as a Markov process with successive published results shiftin
59 ented that use the theory of continuous-time Markov processes with discontinuous sample paths.