A continuous optimization approach for inferring parameters in mathematical models of regulatory networks
© Deng and Tian; licensee BioMed Central Ltd. 2014
Received: 22 November 2013
Accepted: 9 July 2014
Published: 29 July 2014
The advances of systems biology have raised a large number of sophisticated mathematical models for describing the dynamic property of complex biological systems. One of the major steps in developing mathematical models is to estimate unknown parameters of the model based on experimentally measured quantities. However, experimental conditions limit the amount of data that is available for mathematical modelling. The number of unknown parameters in mathematical models may be larger than the number of observation data. The imbalance between the number of experimental data and number of unknown parameters makes reverse-engineering problems particularly challenging.
To address the issue of inadequate experimental data, we propose a continuous optimization approach for making reliable inference of model parameters. This approach first uses a spline interpolation to generate continuous functions of system dynamics as well as the first and second order derivatives of continuous functions. The expanded dataset is the basis to infer unknown model parameters using various continuous optimization criteria, including the error of simulation only, error of both simulation and the first derivative, or error of simulation as well as the first and second derivatives. We use three case studies to demonstrate the accuracy and reliability of the proposed new approach. Compared with the corresponding discrete criteria using experimental data at the measurement time points only, numerical results of the ERK kinase activation module show that the continuous absolute-error criteria using both function and high order derivatives generate estimates with better accuracy. This result is also supported by the second and third case studies for the G1/S transition network and the MAP kinase pathway, respectively. This suggests that the continuous absolute-error criteria lead to more accurate estimates than the corresponding discrete criteria. We also study the robustness property of these three models to examine the reliability of estimates. Simulation results show that the models with estimated parameters using continuous fitness functions have better robustness properties than those using the corresponding discrete fitness functions.
The inference studies and robustness analysis suggest that the proposed continuous optimization criteria are effective and robust for estimating unknown parameters in mathematical models.
In systems biology, mathematical modelling plays an important role in identifying regulatory mechanisms of biochemical systems. These models have been applied successfully to study dynamic interactions among system components and simulate systems responses to external signals. Such an important tool offers enormous potential for exploring system functions at various levels and also serves as the test beds for generating hypotheses and designing biological experiments. However, one of the major challenges in mathematical modelling is the unknown model parameters that are estimated from experimentally measured quantities. Although part of the model parameters may be calculated directly from experimental data, such as the protein degradation rate that can be obtained from the half-life of the protein, the majority of model parameters has to be estimated by matching computer simulations to experimental data. In spite of substantial progresses achieved in the last 20 years, this reverse-engineering problem still remains a challenge in computational biology [1, 2]. The key issue is how to infer a large number of model parameters from a small number of experimental data . Moreover, this reverse-engineering problem has been extended from parameter estimation to model selection [4, 5].
There are two major types of approaches for estimating model parameters. The first approach uses optimization techniques to find the optimal parameter sets . These optimization methods usually convert parameter inference into a functional optimization problem and then minimize the objective function that measures the goodness-of-fit of the model according to the given experimental data. Two major types of optimization methods in the literature are called gradient-based optimization methods and evolutionary-based optimization methods. Based on these two basic approaches, various techniques such as simulated annealing, linear and non-linear least-squares fitting, genetic algorithms and evolutionary computation have been employed to build computational biology models [6–9]. In addition, to address the key issue of local maxima in optimization methods, deterministic and stochastic global optimization methods have been explored recently in systems biology .
Another type of inference methods is statistical methods including the Bayesian inference methods [11–14]. The major advantage of these methods is the ability to infer the whole probability distribution of parameters, rather than a single optimal estimate. In addition, they can deal with noisy data and uncertain data. Recent advances in Bayesian computation including Markov chain Monte Carlo (MCMC) techniques and sequential Monte Carlo (SMC) methods that have been successfully applied to infer models of biological systems [15, 16]. However, the potential obstacles of these methods in application include the potential correlation of generated samples, dependence of algorithm performance on prior hypothesis, and requirement of likelihood function. To address these issues, for example, for parameter estimation problems without analytically likelihoods, approximate Bayesian computation (ABC) methods have been designed to provide stable parameter estimates with relatively high computational efficiency , and thus have been applied to a wide range of models in systems biology . Most recently, we have proposed two algorithms to improve the performance of ABC algorithms using the simulated likelihood density .
Each inference method mentioned above has its advantages and disadvantages. It is difficult to find an inference method that is effective to all the biological models and is better than all the other methods . We may develop inference methods that are good enough within the given tolerances. There are a number of criteria to measure the quality of an inference method, including the efficiency regarding the computing time, flexibility about changing systems constraints, and robustness to the noise in experimental data . In addition, a good inference algorithm should have less local minima in order to accelerate the convergence rate of optimization algorithms . Currently the widely used objective functions are based on the least-squared error criterion or more sophisticated weighted objective functions for deterministic models [7, 9, 22] or likelihood functions for stochastic models [23, 24]. To address the issue of local maxima, a number of objective functions have been proposed using smoothness conditions of simulations such as the slope error criterion  and the second derivative criterion . In addition, the combination of different objective functions leads to more sophisticated multiple-objective approaches that embed different sources of information into a single computational framework [26, 27].
Another important characterisitcs of inference methods is the identifiability, namely whether the model parameters can be uniquely determined by the given experimental data [2, 28]. When the number of experimental data is less than the number of unknown parameters, the inverse problem is non-identifiable. To address the issue of insufficient data, we used experimental data at measurement time points and a linear interpolation to generate more data at other time points . In this work we go one step further by proposing a novel approach to infer unknown parameters in mathematical models. In addition to minimize the difference between simulation and experimental data at the measurement time points using existing methods, the innovation of this approach is to reduce potential errors at non-measurement time points. To achieve this, we propose to use a cubic spline interpolation to generate continuous representation of system dynamics and calculate simulation errors over the entire time interval of the observation. Based on the least-squared error criterion, we propose a number of continuous approaches using function values as well as the first and second order derivatives. Although the continuous representation of systems dynamics has been employed for other problems such as the continuous representation of microarray gene expression data , this is the first time that it is used to infer model parameters. Following this, three case studies are presented to demonstrate the effectiveness and accuracy of the proposed continuous approaches.
where denotes the slope of experimental data for the i-th component at time point t j , and is the numerical derivative of the i-th simulated component at t j .
where X′′ i (t j ) is the second derivative of X i (t j ). These criteria are designed either to reduce the errors of the second order derivatives (6, 7) or to decrease the “roughness” of the solution, and hence to relieve the overfitting problem (8, 9) .
In addition, there are potentially some large simulation errors at the non-measurement time points even when the simulation is in good agreement with experimental data at the measurement time points. To improve the reliability of inference, one approach is to generate observation data at a number of non-measurement time points by using a linear interpolation . However, such a low order interpolation may generate errors to the generated observation data and further influence the accuracy of inferred model parameters. To improve the accuracy, this technique can be extended in one of the following two ways: we may either use a higher order interpolation method or estimate observation data at more non-measurement time points. The extreme case of the latter approach is to use the whole trajectory rather than observations at discrete time points to calculate the difference between simulated and experimental data. Here we use this approach to develop a continuous optimization method to infer model parameters reliably.
Fitness functions for measuring simulation error
Discrete absolute error of function values
Discrete absolute error of function and derivative values
(2, 4, 6)
Discrete absolute error of function, derivative, second derivative values
(2, 4, 8)
Discrete absolute error of function, derivative values as well as values of second derivative.
Discrete relative error of function values
Discrete relative error of function and derivative values
(3, 5, 7)
Discrete relative error of function, derivative, second derivative values
(3, 5, 9)
Discrete relative error of function, derivative values as well as values of second derivative.
Continuous absolute error of function values
Continuous absolute error of function and derivative values
(10, 12, 14)
Continuous absolute error of function, derivative, second derivative values
(10, 12, 16)
Continuous absolute error of function, derivative values as well as values of second derivative.
Continuous relative error of function values
Continuous relative error of function and derivative values
(11, 13, 15)
Continuous relative error of function, derivative, second derivative values
(11, 13, 17)
Continuous relative error of function, derivative values as well as values of second derivative.
Cubic spline interpolation
for i = 1, …, m - 1. The cubic spline S(t) will interpolate all data points. In addition, the function, first and second derivatives are continuous for the interval [t1, t m ]. Compared with the piece-wise linear interpolation, a cubic spline function has two major advantages: a higher order of approximation to increase approximation accuracy and smoothness of first and second derivatives. The latter is important in this work since we include the first and second derivatives of simulation/observation to measure simulation errors.
There are various types of the cubic spline functions depending on different boundary conditions. Denoting the second derivative of the spline as M i = S′′ (t i ), three examples of cubic spline interpolation are natural spline (M1 = M m = 0), parabolic spline (M1 = M2, Mm - 1 = M m ) and cubic runout spline (M1 = 2M2 - M3, M m = 2Mm - 1 - Mm - 2). This work uses the natural spline interpolation to generate continuous functions for numerical solutions of system (Eq. 1) and for experimental data.
All model parameters are estimated using a genetic algorithm, which is an effective searching method for finding unknown kinetic rates when the search space is associated with a complex error landscape. We use a MATLAB toolbox developed by Chipperfield et al.  to infer the unknown model parameters. This toolbox uses MATLAB functions to build a set of versatile routines for implementing a wide range of genetic algorithms. The major procedures of the genetic algorithm toolbox include population representation and initiation, fitness assignment, selection functions, crossover operators, mutation operators and multiple subpopulation support. In this work we use the function crtbp to create the binary initial population. The linear-ranking and non-linear-ranking algorithm ranking is used to transform the raw objective function values into non-negative figures of merit for each individual. In addition, a selection function reins is used to effect fitness-based reinsertion when the entire population is not reproduced in each generation, and a high-level entry function select is used to provide a convenient interface to the selection routines. Finally, a high-level entry function recombine and the routine mut are applied to provide all the crossover operators and perform binary and integer mutations.
In our numerical tests, the genetic algorithm run over 300 generations for each estimate and there are a population of 100 individuals in each generation. The estimation error generally remains unchanged after the 200th generation in each implementation. The value of a model parameter is taken initially from the uniform distribution in the range of [0,Wmax]. Here Wmax is the maximal possible value of that parameter. Different parameters may have different values of Wmax. The initial estimate of rate constants can be changed by using different random seeds in the MATLAB toolbox, leading to different final estimates of the model parameters. We use different seeds of random numbers in MATLAB to generate different initial sets of model parameters in the genetic algorithm. For each initial set of parameters, we simulate the mathematical model to obtain the time-course profiles of the system. Different criteria listed in Table 1 are used in the genetic algorithm as the objective function to calculate the difference between numerical and standard simulations. For the discrete criteria, we simply compare the differences between the simulated and exact data at each measurement time point. However, when using the continuous criteria, we use a cubic spline to obtain the continuous function as well as its first and second derivatives for both experimental data and numerical solutions. The calculated fitness value is then returned to genetic algorithm for selecting the optimal model parameters.
Accuracy of the estimated model parameters
To treat each parameter equally, we choose relative errors to measure the difference between the estimated parameters and model parameters. This mean error is a measure for accuracy property of each criterion. In addition, we present standard deviation (STD) for these 10 sets of estimates as additional information for the quality of estimates. However, the comparison of discrete and continuous approaches is mainly based on the magnitude of the mean errors of these approaches.
where is the numerical solution of the i-th component at time point t j using the perturbed parameters, and x ij is the corresponding simulated data without parameter perturbation. In addition, the standard deviation of simulation errors is used to measure the fluctuations of perturbed simulations.
with the Gaussian random variable N(0,1). Here μ = 0.2 is the perturbation strength for the first and second systems and μ = 0.1 for the third system. We have also tested other values of strength. When the value of μ is small, the difference between the robustness properties is too small to distinguish for different methods. However, if this value is large, the model with perturbed parameters may be stiff and numerical solutions may blow out.
Then we calculate the mean and standard deviation (STD) of the variance ϵ l . For each criterion, we considere the top 10 sets of estimated parameters that have the smallest values of the fitness function. The mean and STD of the variation ϵ l for each set of parameter are averaged, which are used as the final results presented in Additional file 1: Tables S6, S7 and S8.
The ERK kinase activation module
where [M] and [E] are the concentrations of MEK and ERK, respectively, and [Mpp-E] represents complex [MEKpp-ERK].
and initial condition [0.165, 5, 0, 0, 0, 0] (in Figure three in ). The generated simulation is used as the standard simulation which is very close to the experimental data (Additional file 1: Figure S1). The natural cubic spline is used to calculate the first and second derivatives of the standard simulation. Then we use a genetic algorithm to search for the optimal model parameters . The values of Wmax for these 6 parameters all are equal to 300.
Summary of the accuracy of the estimated model parameters
ERK kinase module
G1/S transition module
MAP kinase pathway
The number of the absolute criteria
The number of the relative criteria
Better continuous absolute criteria
CAE1, CAE2, CAE3, CAE4
Better discrete absolute criteria
Better continuous relative criteria
CRE2, CRE3, CRE4
CRE1, CRE2, CRE3, CRE4
Better discrete relative criteria
DRE1, DRE2, DRE3
The best criteria
To find out the reasons for variations in the performance of various criteria, we plot the mean of each estimated model parameter, which is the average of the top 10 estimates for each criterion in Additional file 1: Figure S2. To match the relative errors in Additional file 1: Table S2, the averaged parameters were scaled by the exact parameter; and the exact parameters in Additional file 1: Figure S2 are always unit one. Additional file 1: Figure S2 suggests that the criterion CAE4 (the continuous absolute-error criterion using the first and second derivatives) produces estimates in which each estimated parameter is close to the exact one with moderate errors. However, the discrete relative-error criteria may produce estimates with large errors.
The G1/S transition module
For the 10 parameters in the model, we use the exact values (k1 = 1, Kn1 = 0.5, J11 = 0.5, ϕ pRB = 0.005, k p = 0.05, k2 = 1.6, a = 0.04, Kn2 = 4, J12 = 5, ϕE2F1 = 0.1) and initial conditions [pRB, E2F1] = [1,5]  to generate a standard simulation whose values at t = [0, 50, 100, 150, 200, 250, 300] are used as the experimental data (Additional file 1: Figure S3).
We employed the same approach as used for the first case study to investigate the accuracy of different criteria. The values of Wmax for these 10 parameters all are equal to 5. Numerical results in Table 2 and Additional file 1: Table S3 suggested that, among the absolute-error criteria, the continuous criteria always generate more accurate estimates than the corresponding discrete criteria. In addition, among all types of continuous criteria, the absolute-error criteria produced more accurate estimates than the relative-error criteria. Therefore, continuous absolute-error criteria are superior to the other criteria in both mean error and STD. In particular, continuous absolute-error criterion of function values (CAE1) has the minimal mean error. Numerical results in the second case study suggested that the continuous absolute-error criteria are effective approaches for inferring unknown parameters in mathematical models.
The MAP kinase pathway
The first two tested models have only small numbers of unknown parameters. Therefore the next question is whether the results obtained from these two small-scale systems are still valid for systems with a large number of unknown parameters. To answer this question, we used a recently proposed model with 57 unknown model parameters as the third test system. This model describes the dynamics of the MAP kinase pathway, which is one of the most prominent signaling pathways . This model comprises a cytosolic subsystem and a nuclear subsystem. In the cytosolic subsystem, the Ras-GTP is the signal input of the MAP kinase cascade, which activates Raf molecules in a single step. This activation is followed by sequential activation of the dual-specificity MAP kinase kinase (MEK) by Raf* (i.e., the activated Raf) in a single-step processive module. The activated MEKpp in turn activates ERK in a two-step distributive module. The activated ERKpp is the signal output of the MAK kinase module [29, 36]. MEK and ERK kinases can diffuse between the cytosol and nucleus freely. In the nuclear subsystem, the activated MEKpp can further activate ERK kinase via the distributive two-step phosphorylation module. In addition, phosphatases, termed as Raf-P’ase, MEK-P’ase and ERK-P’ase, can deactivate the activated Raf*, MEKpp and ERKpp kinases, respectively, at different subcellular locations . The detailed information of phosphorylation and dephosphorylation reactions as well as the differential equation model are given in the Additional file 1.
The extended observation data, namely the proteomic data together with the interpolated data at the time points between the observations, are used to infer the model parameters. The proteomic data are relative protein concentrations, in which the activity of each kinase is normalized by its activity at 5 min. Thus we only use the four relative criteria (DRE1 ~ 4 and CRE1 ~ 4) to infer the model parameters. We also use the kinetic rate constants estimated from the same dataset  to generate a simulation. The rate constants and initial conditions are also provided in the Additional file 1. Additional file 1: Figure S4 gives simulated and observed datasets. Similar to the experimental data, we use the activities of Raf, MEK and ERK kinases to infer parameters. Here MAK and ERK data include the activities in cytosol, nucleus as well as the total activity. We use a stiff-implicit solver ode23tb in MATLAB to simulate mathematical model and apply genetic algorithm to search for optimal model parameters . The cubic spline interpolation is used to calculate the first and second derivatives of the observation data and numerical simulation. The values of Wmax for these 57 unknown parameters all are equal to 300.
For each relative criterion, we estimate 100 sets of parameters and selected the top 10 sets that have the smallest fitness values. Then we compared the relative difference between the estimated parameters and exact rate constants, which were presented in Additional file 1: Table S4. For various fitness functions, the continuous criteria always generated more accurate estimates than the discrete criteria. In particular, among various continuous criteria, the criterion based on the simulation values (CRE1) leads to estimates with the smallest mean error; in addition, the criterion using function values and the first order derivative values (CRE2) produced more stable estimates, which have smaller values of the STD.
rather than by the individual rate constants that are pertinent . Thus we calculated the averaged errors of the factor K mi for each inference method we have tested, which are presented in Additional file 1: Table S5. Numerical results suggest that continuous criterion using the function values (CRE1) generates estimates with the best accuracy and smallest STD.
Due to the lack of experimental data as a constraint in reverse-engineering, the estimated model parameters may have a wide range of values but all of them are able to faithfully realize experimental observations. Currently a few additional criteria, including robustness property, have been used to select the candidates of estimated parameters. Robustness can be defined as the ability of a system to function correctly in the presence of both internal and external uncertainty . Since the robustness property is ubiquitously in biological systems [41, 42], it has been used as a criterion not only to select the optimal network from the candidate structures but also to choose estimated rate constants of mathematical models [43–45]. A formal definition of this property is well consistent with the general principle of robustness property for complex systems [33, 40]. Recently more detailed definitions have been proposed to calculate the robustness property of biological systems .
To demonstrate the reliability of the continuous approach, we then carry out the robustness analysis for the three systems with the selected top 10 estimates of model parameters of each criterion. Here noise in the model represents the combined sources of fluctuations such as errors in estimated parameters, external environmental noise and internal noise due to small numbers of molecules. We first used the estimated kinetic rates without any perturbation to produce a standard simulation. Then for each set of parameters, we generated 5,000 sets of perturbed rate constants using the Gaussian random variable and a perturbation strength μ (Eq. 20). Perturbed simulations were obtained by using the perturbed parameters, and we compared the standard simulation with perturbed simulations. Based on the definition of robustness (Eq. 19), we used the mean and STD of simulation errors to represent the robustness property. The system with a particular set of rate constants is more stable if both the mean and STD of simulation errors are smaller.
Summary of the robustness property of the three models with estimated model parameters
ERK kinase module
G1/S transition module
MAP kinase pathway
The number of the absolute criteria
The number of the relative criteria
Better continuous absolute criteria
CAE1, CAE3, CAE4
Better discrete absolute criteria
Better continuous relative criteria
CRE2, CRE3, CRE4
CRE1, CRE2, CRE3
Better discrete relative criteria
DRE1, DRE2, DRE3
This work presents a continuous optimization approach to address the issue of inadequate experimental data for inferring unknown parameters in mathematical models of biochemical networks. The proposed method is based on the approximation of a cubic spline function to the underlying solution of the network model. In addition to the function values that are widely used in the existing approaches, both the first and second derivatives of the simulation are also required to match the generated observation data using a cubic spline function. Therefore the success of this approach depends on the approximation of the cubic spline to the solution of network model. Another important factor to determine the success of continuous approaches may be the relative amount of added data using continuous approaches. Compared with the experimental observation data, the second model (i.e. the G1/S transition module) has less generated observation data using the continuous approaches; while the third model (i.e. the MAP kinase pathway) has much more generated observation data. The performance of continuous approaches for the third model is better than the corresponding discrete approaches. However, using continuous approaches for the second model is just as good as discrete approaches. Thus our results suggest that the performance of these continuous methods will be better if continuous approaches can generate more observation data.
For the three test models, numerical simulations using estimated model parameters match the continuous system dynamics based on experimental data very well. However, numerical results suggest that the first derivative of the system dynamics contributes the majority of simulation error. Thus new methods are needed to reduce the approximation error of the first derivative. This observation may give an explanation for the small difference between criteria 3 and 4, namely the criterion using the error of the second derivative and that using the maximal value of the second derivative. However, it will be interesting to examine the importance of higher order derivatives and consider other types of approximation methods in order to consider approximations using higher order derivatives.
It is assumed in this work that there is no noise in experimental measurement. However, the datasets from biological experiments are often subject to environmental fluctuations and measurement error. Noise at one measurement point will be propagated to the function values at other time points via interpolation function. Thus it may have substantial impact on the accuracy of estimated parameters. Since spline is a piecewise continuous interpolation, our approach can ensure that the influence of noise is constrained to a relatively small time period. Recently a number of approaches have been proposed to filter out noise from experimental observations, including the particle filtering method . Thus an interesting topic is to combine these noise-filtering methods with the continuous optimization approach to make reliable estimation of unknown parameters.
The calculation of simulation error is also an important issue in parameter estimation. This work considered two types of error, namely absolute error and relative error. An interesting result is that using criteria based on absolute error lead to estimates with better accuracy, though it was widely accepted that the advantage of using relative error is to avoid the dominance of large errors derived from parameters with large value. When all the parameter values are moderate in the second test system, there is no substantial difference between the estimates derived from absolute error or relative error. Regarding the calculation of simulation error, a more sophisticated approach is using the weighted distance measure , which would be a topic of interest in further study.
Our proposed continuous approach represents a new starting point to design inference methods to estimated unknown parameters in mathematical models. Nearly all current inference methods are discrete methods using experimental data at a number of measurement time points. Thus we may design corresponding continuous approaches based on these discrete approaches. The key issue is whether the continuous inference method is better than the corresponding discrete method in terms of accuracy and reliability. In this work we compared the accuracy of four discrete inference methods with that of the corresponding continuous methods. In fact these discrete methods are current in use for estimating model parameters [20, 29, 31]. Thus this work provided promising evidence showing that the continuous approaches perform better than the corresponding discrete methods for the three test systems.
In summary, this work proposes an effective continuous optimization approach for estimating model parameters in mathematical models of biological systems. This method uses a spline function to approximate the underlying solution of the network model. The spline function generates observation data at other time points together with the first and second derivatives of the network simulation. All the generated information is used to infer unknown parameters in mathematical models. This work represents an early attempt to address the issue of inadequate experimental data for estimating unknown parameters. Three case studies are used to verify the accuracy of the proposed approaches. Simulation results suggest that the proposed continuous optimization method is an effective and robust approach for accurate and reliable parameter estimation.
T.T. is an Australian Research Council (ARC) Future Fellow (FT100100748). T.T. is also supported by grant from the ARC (DP120104460).
- Hartig F, Calabrese JM, Reineking B, Wiegand T, Huth A: Statistical inference for stochastic simulation models–theory and application. Ecol Lett. 2011, 14 (8): 816-827.View ArticlePubMedGoogle Scholar
- Ashyraliyev M, Fomekong-Nanfack Y, Kaandorp JA, Blom JG: Systems biology: parameter estimation for biochemical models. Febs J. 2009, 276 (4): 886-902.View ArticlePubMedGoogle Scholar
- Gutenkunst RN, Waterfall JJ, Casey FP, Brown KS, Myers CR, Sethna JP: Universally sloppy parameter sensitivities in systems biology models. PLoS Comput Biol. 2007, 3 (10): 1871-1878.View ArticlePubMedGoogle Scholar
- Lillacci G, Khammash M: Parameter estimation and model selection in computational biology. PLoS Comput Biol. 2010, 6 (3): e1000696-View ArticlePubMed CentralPubMedGoogle Scholar
- Vyshemirsky V, Girolami MA: Bayesian ranking of biochemical system models. Bioinformatics. 2008, 24 (6): 833-839.View ArticlePubMedGoogle Scholar
- Kirkpatrick S, Gelatt CD, Vecchi MP: Optimization by simulated annealing. Science. 1983, 220 (4598): 671-680.View ArticlePubMedGoogle Scholar
- Mendes P, Kell D: Non-linear optimization of biochemical pathways: applications to metabolic engineering and parameter estimation. Bioinformatics. 1998, 14 (10): 869-883.View ArticlePubMedGoogle Scholar
- Ashyraliyev M, Jaeger J, Blom JG: Parameter estimation and determinability analysis applied to Drosophila gap gene circuits. BMC Syst Biol. 2008, 2: 83-View ArticlePubMed CentralPubMedGoogle Scholar
- Moles CG, Mendes P, Banga JR: Parameter estimation in biochemical pathways: a comparison of global optimization methods. Genome Res. 2003, 13 (11): 2467-2474.View ArticlePubMed CentralPubMedGoogle Scholar
- Balsa-Canto E, Banga JR, Egea JA, Fernandez-Villaverde A, de Hijas-Liste GM: Global optimization in systems biology: stochastic methods and their applications. Adv Exp Med Biol. 2012, 736: 409-424.View ArticlePubMedGoogle Scholar
- Wilkinson DJ: Bayesian methods in bioinformatics and computational systems biology. Brief Bioinform. 2007, 8 (2): 109-116.View ArticlePubMedGoogle Scholar
- Rogers S, Khanin R, Girolami M: Bayesian model-based inference of transcription factor activity. BMC Bioinformatics. 2007, 8 (Suppl 2): S2-View ArticlePubMed CentralPubMedGoogle Scholar
- Boys RJ, Wilkinson DJ, Kirkwood TBL: Bayesian inference for a discretely observed stochastic kinetic model. Stat Comput. 2008, 18 (2): 125-135.View ArticleGoogle Scholar
- Komorowski M, Finkenstadt B, Harper CV, Rand DA: Bayesian inference of biochemical kinetic parameters using the linear noise approximation. BMC Bioinformatics. 2009, 10: 343-View ArticlePubMed CentralPubMedGoogle Scholar
- Battogtokh D, Asch DK, Case ME, Arnold J, Schuttler HB: An ensemble method for identifying regulatory circuits with special reference to the qa gene cluster of Neurospora crassa. Proc Natl Acad Sci U S A. 2002, 99 (26): 16904-16909.View ArticlePubMed CentralPubMedGoogle Scholar
- Sisson SA, Fan Y, Tanaka MM: Sequential Monte Carlo without likelihoods. Proc Natl Acad Sci U S A. 2007, 104 (6): 1760-1765.View ArticlePubMed CentralPubMedGoogle Scholar
- Beaumont MA, Zhang W, Balding DJ: Approximate Bayesian computation in population genetics. Genetics. 2002, 162 (4): 2025-2035.PubMed CentralPubMedGoogle Scholar
- Marjoram P, Tavare S: Modern computational approaches for analysing molecular genetic variation data. Nat Rev Genet. 2006, 7 (10): 759-770.View ArticlePubMedGoogle Scholar
- Wu Q, Smith-Miles K, Tian T: Approximate Bayesian computation schemes for parameter inference of discrete stochastic models using simulated likelihood density. BMC Bioinformatics. 2014, 15:Google Scholar
- Zhan C, Yeung LF: Parameter estimation in systems biology models using spline approximation. BMC Syst Biol. 2011, 5: 14-View ArticlePubMed CentralPubMedGoogle Scholar
- Voss HU, Timmer J, Kurths J: Nonlinear dynamical system identification from uncertain and indirect measurements. Int J Bifurcat Chaos. 2004, 14 (6): 1905-1933.View ArticleGoogle Scholar
- Wang J, Tian T: Quantitative model for inferring dynamic regulation of the tumour suppressor gene p53. BMC Bioinformatics. 2010, 11: 36-View ArticlePubMed CentralPubMedGoogle Scholar
- Tian T, Xu S, Gao J, Burrage K: Simulated maximum likelihood method for estimating kinetic rates in gene expression. Bioinformatics. 2007, 23 (1): 84-91.View ArticlePubMedGoogle Scholar
- Wang YF, Christley S, Mjolsness E, Xie XH: Parameter inference for discretely observed stochastic kinetic models using stochastic gradient descent. BMC Syst Biol. 2010, 4: 99-View ArticlePubMed CentralPubMedGoogle Scholar
- Liu PK, Wang FS: Inference of biochemical network models in S-system using multiobjective optimization approach. Bioinformatics. 2008, 24 (8): 1085-1092.View ArticlePubMedGoogle Scholar
- Gupta R, Stincone A, Antczak P, Durant S, Bicknell R, Bikfalvi A, Falciani F: A computational framework for gene regulatory network inference that combines multiple methods and datasets. BMC Syst Biol. 2011, 5: 52-View ArticlePubMed CentralPubMedGoogle Scholar
- Tian T, Smith-Miles K: Mathematical modeling of GATA-switching for regulating the differentiation of hematopoietic stem cell. BMC Syst Biol. 2014, 8 (Suppl 1): S8-View ArticlePubMed CentralPubMedGoogle Scholar
- Rateitschak K, Winter F, Lange F, Jaster R, Wolkenhauer O: Parameter identifiability and sensitivity analysis predict targets for enhancement of STAT1 activity in pancreatic cancer and stellate cells. PLoS Comput Biol. 2012, 8 (12): e1002815-View ArticlePubMed CentralPubMedGoogle Scholar
- Tian T, Song J: Mathematical modelling of the MAP kinase pathway using proteomic datasets. PLoS One. 2012, 7 (8): e42230-View ArticlePubMed CentralPubMedGoogle Scholar
- Bar-Joseph Z, Gerber G, Simon I, Gifford DK, Jaakkola TS: Comparing the continuous representation of time-series expression profiles to identify differentially expressed genes. Proc Natl Acad Sci U S A. 2003, 100 (18): 10146-10151.View ArticlePubMed CentralPubMedGoogle Scholar
- Voit EO, Almeida J: Decoupling dynamical systems for pathway identification from metabolic profiles. Bioinformatics. 2004, 20 (11): 1670-1681.View ArticlePubMedGoogle Scholar
- Chipperfield AJ, Fleming PJ, Fonseca CM: Genetic Algorithm Tools for Control Systems Engineering. Proceedings of Adaptive Computing in Engineering Design and Control. 1994, Plymouth Engineering Design Centre, 128-133.Google Scholar
- Kitano H: Towards a theory of biological robustness. Mol Syst Biol. 2007, 3: 137-View ArticlePubMed CentralPubMedGoogle Scholar
- Ferrell JE, Bhatt RR: Mechanistic studies of the dual phosphorylation of mitogen-activated protein kinase. J Biol Chem. 1997, 272 (30): 19008-19016.View ArticlePubMedGoogle Scholar
- Bhalla US, Ram PT, Iyengar R: MAP kinase phosphatase as a locus of flexibility in a mitogen-activated protein kinase signaling network. Science. 2002, 297 (5583): 1018-1023.View ArticlePubMedGoogle Scholar
- Tian T, Harding A, Inder K, Plowman S, Parton RG, Hancock JF: Plasma membrane nanoswitches generate high-fidelity Ras signal transduction. Nat Cell Biol. 2007, 9 (8): 905-914.View ArticlePubMedGoogle Scholar
- Tian TH: Estimation of Kinetic Rates of MAP kinase Activation from Experimental Data. 2009 International Joint Conference on Bioinformatics, Systems Biology and Intelligent Computing, Proceedings. 2009, Washington DC, USA: IEEE Computer Society, 457-462.View ArticleGoogle Scholar
- Swat M, Kel A, Herzel H: Bifurcation analysis of the regulatory modules of the mammalian G1/S transition. Bioinformatics. 2004, 20 (10): 1506-1511.View ArticlePubMedGoogle Scholar
- Huang CY, Ferrell JE: Ultrasensitivity in the mitogen-activated protein kinase cascade. Proc Natl Acad Sci U S A. 1996, 93 (19): 10078-10083.View ArticlePubMed CentralPubMedGoogle Scholar
- Bates DG, Cosentino C: Validation and invalidation of systems biology models using robustness analysis. IET Syst Biol. 2011, 5 (4): 229-244.View ArticlePubMedGoogle Scholar
- Kitano H: Biological robustness. Nat Rev Genet. 2004, 5 (11): 826-837.View ArticlePubMedGoogle Scholar
- Tian T, Olson S, Whitacre JM, Harding A: The origins of cancer robustness and evolvability. Integr Biol (Camb). 2011, 3 (1): 17-30.View ArticleGoogle Scholar
- Citri A, Yarden Y: EGF-ERBB signalling: towards the systems level. Nat Rev Mol Cell Biol. 2006, 7 (7): 505-516.View ArticlePubMedGoogle Scholar
- Apri M, Molenaar J, de Gee M, van Voorn G: Efficient estimation of the robustness region of biological models with oscillatory behavior. PLoS One. 2010, 5 (4): e9865-View ArticlePubMed CentralPubMedGoogle Scholar
- Masel J, Siegal ML: Robustness: mechanisms and consequences. Trends Genet. 2009, 25 (9): 395-403.View ArticlePubMed CentralPubMedGoogle Scholar
- Rizk A, Batt G, Fages F, Soliman S: A general computational method for robustness analysis with applications to synthetic gene networks. Bioinformatics. 2009, 25 (12): i169-i178.View ArticlePubMed CentralPubMedGoogle Scholar
- Huys QJ, Paninski L: Smoothing of, and parameter estimation from, noisy biophysical recordings. PLoS Comput Biol. 2009, 5 (5): e1000379-View ArticlePubMed CentralPubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.