Difference between revisions of "Support:Documents:COMKAT Examples"

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= Example 1: [[Examples: Estimate Input Parameters, Rate Constants Known]] =
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== Official Examples ==
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= Example 2: [[Simplified reference tissue method]] =
 
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= Example 3: [[Glucose Minimal Model]] =
 
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= Example 4: [[Enzyme-substrate (Michaelis-Menten) kinetics]] =
 
  
 +
* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_physiological_parameters_using_a_physiologically_based_model A physiologically based model]
  
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= Example 1: Estimate Input Parameters, Rate Constants Known =
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_Parametric_Image_with_Matlab_Distributed_Computing_Server Estimate Parametric Image with Matlab Distributed Computing Server]
  
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= Simplified reference tissue method =
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Model_Corrected_Input_Function Model Corrected Input Function]
  
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This example demonstrates a COMKAT implementation of the simplified reference tissue model (SRTM) described by Lammertsma and Hume [Neuroimage. 4(3 Pt 1), 153-158 (1996)]. By simultaneously analyzing time-activity curves from areas with and without receptors, the SRTM provides a means to estimate the binding potential which is an index of receptor concentration and ligand affinity.
+
* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_Change_of_Neurotransmitter Estimate Changes of Neurotransmitter after a Stimulus (ntPET)]
  
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==Background==
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_Input_Delay_and_Rate_Constants Estimate Input Delay and Rate Constants]
  
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Input functions are a fundamental component of pharmacokinetic modeling. They describe the time-course of (radio)pharmaceutical which is accessible to the extravascular space. In PET receptor studies the arterial plasma concentration of a ligand is taken as the input function. As there is desire to obviate blood sampling, the SRTM is a popular method used to analyze ligand-receptor data.
+
* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_Input_Parameters%2C_Rate_Constants_Known Estimate Input Parameters, Rate Constants Known]
  
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The typical model equations used for a region containing receptors include state equations for free (F) and bound (B) ligand:
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Estimate_Input_Parameters_Simultaneously_with_Flow Estimate Input Parameters Simultaneously with Flow]
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507">dF/dt = k1 Cp &#8211; (k2+k3)F + k4 B </td>
 
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    <td width="105">Eq 1 </td>
 
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  </tr>
 
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  <tr>
 
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    <td width="507">dB/dt = k3 F &#8211; k4 B</td>
 
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    <td width="105">Eq 2 </td>
 
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  </tr>
 
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</table>
 
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where Cp is the arterial plasma input function and tracer conditions are assumed (B << Bmax) so that k3 = kon (Bmax – B) ≈ kon Bmax.
 
  
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Model Figure
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Simplified_reference_tissue_method Simplified reference tissue method]
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<br>[[Image:ModelFigure.PNG]]
 
  
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In a region devoid of receptors, k3 (and therefore B) is zero so Eq 1 may be simplified. Denoting this region as the reference region, or rr, the equation is
+
* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Glucose_Minimal_Model Glucose Minimal Model]
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">dF<sub>rr</sub>/dt = k1 Cp &#8211; k2<sub>rr</sub> F<sub>rr</sub>  </td>
 
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    <td width="105">Eq 3 </td>
 
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  </tr>
 
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</table>
 
  
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This may be rearranged to obtain an expression for the plasma input
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Enzyme-substrate_%28Michaelis-Menten%29_kinetics Enzyme-substrate (Michaelis-Menten) kinetics]
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52"> Cp = Cpn / k1<sub>rr</sub></td>
 
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    <td width="105">Eq 4 </td>
 
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  </tr>
 
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</table>
 
  
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where
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:FDG_with_Time-varying_Rate_Constants FDG with Time-varying Rate Constants]
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<table width="622" height="66" border="0">
 
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  <tr>
 
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    <td width="507" height="52"> Cpn = (dF<sub>rr</sub>/dt + k2<sub>rr</sub> F<sub>rr</sub>)</td>
 
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    <td width="105">Eq 5 </td>
 
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  </tr>
 
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</table>
 
  
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is the normalized plasma input function.
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* [http://comkat.case.edu/index.php?title=3D_Reslicing_using_COMKAT_image_tool_(basic) 3D Slicing using COMKAT Image Tool (basic)]
  
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This expression (Eq 4) for Cp may be substituted into the equations for regions that have receptors, aka, target tissue which we denote as tt
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* [http://comkat.case.edu/index.php?title=Support%3ADocuments%3AExamples%3A_Reslicing_using_COMKAT_image_tool_(advanced) 3D Slicing using COMKAT Image Tool (advanced)]
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">dF<sub>tt</sub>/dt = (k1<sub>tt</sub>/k1<sub>rr</sub>) Cpn &#8211; (k2<sub>tt</sub>+k3<sub>tt</sub>)F<sub>tt</sub> + k4<sub>tt</sub> B<sub>tt</sub> </td>
 
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    <td width="105">Eq 6 </td>
 
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  </tr>
 
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  <tr>
 
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    <td width="507" height="47">dB<sub>tt</sub>/dt = k3<sub>tt</sub> F<sub>tt</sub> &#8211; k4<sub>tt</sub> B<sub>tt</sub></td>
 
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    <td width="105">Eq 7 </td>
 
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  </tr>
 
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</table>
 
  
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Data from target tissue and from reference regions could be, in theory, simultaneously fit using the model embodied in Eq. 4 to 6. In practice there is often an issue of identifiability. Hence, assumptions are made to reduce the number of parameters to estimate. One assumption is that the equilibrium concentration ratio between plasma and tissue free space is the same in the reference region and target tissue:
 
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">k1<sub>tt</sub>/  k2<sub>tt</sub>= k1<sub>rr</sub> /k2<sub>rr</sub></td>
 
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    <td width="105">Eq 8 </td>
 
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  </tr>
 
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</table>
 
  
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this implies
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== User-contributed Examples ==
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">k1<sub>tt</sub>/k1<sub>rr</sub> =  k2<sub>tt</sub>/k2<sub>rr</sub></td>
 
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    <td width="105">Eq 9 </td>
 
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  </tr>
 
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</table>
 
  
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and this ratio may be denoted by R1
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* [http://comkat.case.edu/index.php?title=Support:Documents:Examples:Instructions_for_Adding_Your_Own_Example Instructions for Adding Your Own Example]
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">R1 = k1<sub>tt</sub>/k1<sub>rr</sub> =  k2<sub>tt</sub>/k2<sub>rr</sub></td>
 
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    <td width="105">Eq 10 </td>
 
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  </tr>
 
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</table>
 
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Making the substitution into Eq 6 we obtain
 
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">dF<sub>tt</sub>/dt = R1 Cpn &#8211; (k2<sub>tt</sub>+k3<sub>tt</sub>)F<sub>tt</sub> + k4<sub>tt</sub> B<sub>tt</sub> </td>
 
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    <td width="105">Eq 11 </td>
 
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  </tr>
 
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</table>
 
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This equation could be solved simultaneously with Eq. 7 to obtain time-courses of free and bound radioligand. Analytic solutions derived for more general conditions (Eq 1 and 2) are given in the appendix in the document thad describes validation of the COMKAT implementation of the FDG model. Solutions for Ftt and B tt would then be summed to obtain the total concentration in the target tissue which is the quantity measured in an imaging study
 
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="52">C<sub>t</sub><sub></sub> = F<sub>tt</sub>+B<sub>tt</sub> </td>
 
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    <td width="105">Eq 12 </td>
 
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  </tr>
 
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</table>
 
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In general, the solution Ctt is a weighted sum of two exponential terms. For ligands in which the association and dissociation of ligand from the receptor is much faster than the transport of ligand between the vascular and extravascular space, two exponentials are not evident from the data. That is, a single exponential model adequaltey describes the data because the two compartments exchange so quickly that they look like a single compartment. (Mathematically one of the eigenvalues or exponential coefficients is very large in magnitude.) The differential equation for such a single-exponential model is
 
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="45">dC<sub>tt</sub> /dt = k1<sub>tt </sub>Cp &#8211;k2<sup>a</sup><sub>tt</sub> C <sub>tt</sub> </td>
 
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    <td width="105">Eq 13 </td>
 
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  </tr>
 
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</table>
 
−
 
 
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where k2att is the the apparent k2tt and is related to the the other parameters as
 
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<table width="622" border="0">
 
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  <tr>
 
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    <td width="507" height="45">k2<sup>a</sup><sub>tt</sub> = k2<sub>tt </sub>/(1+BP)<sub></sub> </td>
 
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    <td width="105">Eq 14 </td>
 
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  </tr>
 
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</table>
 
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where BP = k3tt/k4tt is the binding potential. Expressing the input in terms of Cpn, this is equivalent to the one-tissue compartment model depicted below
 
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Simplified Model Figure
 
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[[Image:SimplifiedModelFigure.png]]
 
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== COMKAT Implementation ==
 
−
 
 
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comkat\examples\dasbSRTM.m
 
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Step 1 To set this up in MATLAB, create an input function that implements Eq. 5 [Cpn = (dFrr/dt + k2rr Frr)]. In this k2rr is a parameter to estimate amd Frris taken as experimentally measured reference region concentration. To obtain Frr at arbitrary times requires interpolation. For this a smoothing spline is used. Its piecewise-polynomial coefficients are easily obtained
 
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ppCref = csaps(tref, Cref, 0.01);
 
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where tref and Cref are the sample times and concentrations from the reference region. With Frr expressed in this form, the polynomials may be analytically differentiated once to obtain the piecewise polynomial coefficients of dFrr/dt
 
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ppdCrefdt = fnder(ppCref, 1);
 
−
 
 
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The input Cpn may be evaluated as Cpn(t) = k2rr x ppval(ppCref. t) + ppval(ppdCrefdt.t) with the complete function given in comkat\examples\refInput.m
 
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function [Cpn, dCpndk2ref] = refInput(k2ref, t, pxtra)
 
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  ppCref = pxtra{1};
 
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  ppdCrefdt = pxtra{2};
 
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  if (nargout > 0),
 
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    Cpn = k2ref * ppval(ppCref, t) + ppval(ppdCrefdt,t);
 
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    idx = find(Cpn < 0);
 
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    Cpn(idx) = 0;
 
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    if (nargout > 1),
 
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      dCpndk2ref = ppval(ppCref, t);
 
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      dCpndk2ref(idx) = 0;
 
−
    end
 
−
  end
 
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return
 
−
 
 
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For the sake of estimating the value of k2rr, this function must provide the derivative of Cpn with respect to k2rr when two output arguments are requested.
 
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This input function is included in the compartment model by using these commands
 
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sa = 1; % specific activity
 
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dk = 0; % decay constant (=0 since data are decay corrected)
 
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xparm = { ppCref, ppdCrefdt };
 
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cm = addInput(cm, 'Cpn', sa, dk, 'refInput', 'k2ref', xparm);
 
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Step 2 Create a model. To simultaneously fit three regions – midrbain, amygdala, and thalamus – create a model that has the compartments and links depicted as shown. Three Region Model
 
−
 
 
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[[Image:ThreeROIFigureSRTM.PNG]]
 
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The commands are
 
−
 
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% specify compartments
 
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cm = addCompartment(cm, 'Cmid');
 
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cm = addCompartment(cm, 'Camy');
 
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cm = addCompartment(cm, 'Ctha');
 
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cm = addCompartment(cm, 'Sink'); % comkat requires closed system
 
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% specify links
 
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cm = addLink(cm, 'L', 'Cpn',  'Cmid',  'R1mid');  % connect input to
 
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cm = addLink(cm, 'K', 'Cmid', 'Sink',  'k2ppmid');
 
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cm = addLink(cm, 'L', 'Cpn',  'Camy',  'R1amy');
 
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cm = addLink(cm, 'K', 'Camy', 'Sink',  'k2ppamy');
 
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cm = addLink(cm, 'L', 'Cpn',  'Ctha',  'R1tha');
 
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cm = addLink(cm, 'K', 'Ctha', 'Sink',  'k2pptha');
 
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% specify outputs (neglect vascular contrib) 
 
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% for simultaneously fitting target tissues
 
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cm = addOutput(cm, 'Mid', {'Cmid', 'PV'}, { } );
 
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cm = addOutput(cm, 'Amy', {'Camy', 'PV'}, { } );
 
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cm = addOutput(cm, 'Tha', {'Ctha', 'PV'}, { } );
 
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% specify parameters and values
 
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cm = addParameter(cm, 'PV',    1);
 
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cm = addParameter(cm, 'k2ref', 0.05);
 
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cm = addParameter(cm, 'R1mid', 0.8);
 
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cm = addParameter(cm, 'R1amy', 1.0);
 
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cm = addParameter(cm, 'R1tha', 1.2);
 
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cm = addParameter(cm, 'BPmid', 0.5);
 
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cm = addParameter(cm, 'BPamy', 1.0);
 
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cm = addParameter(cm, 'BPtha', 1.5);
 
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cm = addParameter(cm, 'k2ppmid', 'k2ref*R1mid/(1+BPmid)');
 
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cm = addParameter(cm, 'k2ppamy', 'k2ref*R1amy/(1+BPamy)');
 
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cm = addParameter(cm, 'k2pptha', 'k2ref*R1tha/(1+BPtha)');
 
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The rest of the details are quite straightforward and are all contained in the example file comkat\examples\dasbSRTM.m. The only thing slightly unusual is that multiple time-activity curves must be specified so they can be simultaneously fit. To do this, just use
 
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cm = set(cm, 'ExperimentalData', PETdata(:, [1 2 3]));
 
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where columns [1 2 3] contain 'Mid', 'Amy', and 'Tha' data [the same order as the adddOutput() commands] and the rows of PETdata correspond to different frames.
 
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= Glucose minimal model =
 
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This example shows a COMKAT implementation of the glucose minimal model (GMM) which describes the interaction between glucose and insulin in vivo. One model compartment represents interstitial insulin concentration which is denoted by X. Another model compartment represents plasma glucose concentration which is denoted by G. This model was presented in Bergman RN, Ider YZ, Bowden CR, Cobelli C. "Quantitative estimation of insulin sensitivity," Am. J. Physiol., vol. 236, no. 6, pp. E667-E677, June 1979.
 
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== Background ==
 
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Of particular note is that this model has an unusual nonlinear kinetic rule that is different from the nonlinear receptor-ligand and enzyme-substrate kinetic rules. Implementing this GMM in COMKAT required definition of a custom kinetic rule as this example demonstrates. This example also demonstrates COMKAT's ability to solve sensitivity functions (and hence estimate the value of) a parameter which is an initial condition to the differential equations.
 
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Model Equations
 
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<P>dX/dt = -p<SUB>2</SUB> X + p<SUB>3</SUB>(I - I<SUB>b</SUB>)</P>
 
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<P>dG/dt = -GX + p<SUB>1</SUB>(G<SUB>b</SUB> - G)</P>
 
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<P>with initial conditions X = 0, G = p<SUB>4</SUB> at time zero.</P>
 
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X is interstitial insulin concentration. G is plasma glucose concentration. I is plasma insulin concentration. Ib and Gb are basal insulin and glucose concentrations. p1 to p4 are model mathematical parameters. They are related to the physiologically meaningful parameters as follows
 
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* Glucose effectiveness, SG = p1, a measure of the fractional ability of glucose to enhance its own clearance independent of insulin
 
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* Insulin sensitivity, SI = p3/p2, a measure of the dependence of fractional glucose disposal on changes of plasma insulin
 
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* Initial glucose concentration, G(0) = p4
 
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== COMKAT Implementation ==
 
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To implement the unusual non-linear kinetics present for glucose in COMKAT, the glucose state equation is rearranged to obtain
 
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<P>dG/dt = -G(X + p<SUB>1</SUB>) + p<SUB>1</SUB>G<SUB>b</SUB></P>
 
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<P>and the expression (X + p<SUB>1</SUB>) is considered as a rate "constant".
 
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Otherwise, the COMKAT implementation is straighforward and the diagram is depicted below.
 
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Model Diagram
 
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[[Image:ModelFigure_1.PNG]]
 
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Since COMKAT requires a closed system, two junk or sink compartments were created (J1 and J2) so that the efflux from X and G would have a destination.
 
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The complete example is given in comkat\examples\comkatGMM.m.
 
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As the glucose minimal model is used to analze blood sample data (and not an image-based data set) for which people usually assume blood samples represent instantaneous (and not the time-averaged) concentration, this example only considers compartment concentrations (and not the output equations). Accordingly, the plots here are based on solutions to the compartment concentrations which are placed in comp when the model is solved using this command:
 
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[out, outIndex, comp, compIndex] = solve(cm);
 
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<br>Plots of G and X versus time are shown here:
 
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<br>[[Image:compartmentConcentrations.png]]
 
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<br>Compartment Concentrations and plots of compartment sensitivity functions, derivatives of X and G with respect to the model parameters, are shown below
 
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<br>[[Image:GSensitivities.png]]
 
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<br>[[Image:XSensitivities.png]]
 
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<br>Notice that the plots of the sensitivity functions suggest variable X is independent of parameters p1 and p4 as d(X)/d(p1) and d(X)/d(p4) are zero (within the numerical precision). This is expected because a) the state equation for X has neither p1 nor p4 terms and b) G, which appears on the right hand side of the state equation for X, is independent of p1 and p4.
 
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NOTE: GMM is also implemented as part of the validation suite wherein solutions to a COMKAT and an independent implementation are compared.
 
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= Enzyme-substrate (Michaelis-Menten) kinetics =
 
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This example demonstrates COMKAT implementation of enzyme substrate (Michaelis Menten) kinetics. This is a type of kinetic rule in which reaction velocity is saturable. As such, this example demonstrates use of a user-specified custom kinetic rule.
 
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== Background ==
 
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Enzymes act as catalysts speeding up reactions wherein a substrate is converted to product without the enzymes themselves being consumed in the process. When the amount of enzyme is much less than the amount of substrate, the effective rate constant k is not actually a constant but rather depends on the substrate concentration
 
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k = Vmax / (Km + [S])
 
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This relationship is described and derived here and requires a couple of approximations.
 
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A COMKAT implementaion of a model that includes such kinetics is given below. The complete model that avoids the two approximations could also be implemented in COMKAT and will be left as an exercise for the student ;-).
 
−
 
 
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== COMKAT Implementation ==
 
−
 
 
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Model figure
 
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<br>[[Image:ModelFigure_2.png]]
 
−
<br>This example demonstrates how to implement in COMKAT a model that incorporates the Enzyme-Substrate kinetics using a rate "constant" with a value that depends on substrate concentration. In the interest of simplicity, this example only includes only two compartments and one link. Of course more complicated models could be constructed, yet this example is sufficent to demonstrate the concept.
 
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Step 1 To set this up in MATLAB for simulation, create the following function that defines the rate "constant" for this kinetic rule:
 
−
 
 
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function varargout = kinMM(t, c, ncomp, nsens, pName, pValue, pSensIdx, cm, xtra)
 
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  % Michaelis Menten kinetics
 
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  % flux = C * Vmax/(Km + C) so that effective
 
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  % rate constant k = Vmax/(Km + C)
 
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  VmName = pName{1};
 
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  KmName = pName{2};
 
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  VmValue = pValue{1};
 
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  KmValue = pValue{2};
 
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  VmSensIndex = pSensIdx{1};
 
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  KmSensIndex = pSensIdx{2};
 
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  substrateCompartmentIndex = xtra{1};
 
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  if (nargout > 0), % return effective rate constant
 
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    varargout{1} = VmValue / (KmValue + c(substrateCompartmentIndex));
 
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    if (nargout > 1),  % return dk/dc
 
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        dkdc = zeros([1 ncomp]);
 
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        dkdc(substrateCompartmentIndex) = VmValue / (KmValue + c(substrateCompartmentIndex)).^2;
 
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        varargout{2} = dkdc; 
 
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        if (nargout > 2), % return dk/dp
 
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            dkdp = zeros([1 nsens]);
 
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            dkdp(VmSensIndex) = 1 / (KmValue + c(substrateCompartmentIndex));
 
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            dkdp(KmSensIndex) = VmValue / (KmValue + c(substrateCompartmentIndex)).^2;
 
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            varargout{3} = dkdp; % dkdp
 
−
        end
 
−
    end
 
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  end;
 
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  return;
 
−
 
 
−
As for all custom kinetic rules, this function must adhere to the call signature with 8 (or optionally 9) input arguments whether or not all inputs are used. The inputs are
 
−
t       time
 
−
c     Vector of compartment concentrations
 
−
ncomp       Number of compartments in the model
 
−
nsens   Number of parameters for which sensitivity functions are requested (e.g. the number of parameters being estimated_
 
−
pName       Cell array of character strings. E.g. pName{1} = 'Vm', pName{2} = 'Km'
 
−
pValue Cell array with pValue{i} being the value of pName{i}
 
−
pSensIdx    Cell array containing indicies (locations) of pName{i} in the sensitivityName [addSensitivity()] parameters.
 
−
cm   The compartmentModel object
 
−
xtra   Any extra information that the user would like to be passed to the function [this input is optional]
 
−
   
 
−
The kinMM function is bit complicated because it was written to be general. The compartments that are the source and destination of the link are not hardcoded but rather determined based on the value of the input arguments. Likewise, the names of the parameters that are used to identify what are traditionally described as Km and Vmax are also be specified. Not only does this allow a user call the parameter whatever suits his or her fancy (e.g. the Km value could be specified by a parameter called 'Fred'), it also facilitates models with more than one link that is described by enzyme-substrate kinetics. Writing the function to be general in this fashion obviates having to write a separate kinetic rule function for each model. (The newest verion of the function above is available in comkat\examples\kinMM.m).
 
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−
One thing to notice about the function above is that the line
 
−
 
 
−
varargout{1} = VmValue / (KmValue + c(substrateCompartmentIndex));
 
−
 
 
−
corresponds to the equation given in Background.The substrate concentration [S] is taken as the concentration in the source compartment.
 
−
 
 
−
Another thing to notice is that the function should return 0, 1 or more values depending nargout. The first return value would be the value of the rate "constant". The second return value would be the derivaive of the rate constant with respect to the concentration vector. The third return value would be the derivative of the rate constant with respect to the sensitivity parameters. These latter two are used in calculating the derivative of model output with respective to sensitivity parameters which is important in data fitting.
 
−
 
 
−
Step 2 Create the model.
 
−
 
 
−
conc = 10; % initial substrate concentration
 
−
 
−
cm = compartmentModel;
 
−
cm = addCompartment(cm, 'Substrate');
 
−
cm = addCompartment(cm, 'Product');
 
−
cm = addParameter(cm, 'Km', 10);
 
−
cm = addParameter(cm, 'Vm', 0.5);
 
−
cm = addParameter(cm, 'dk', 0); % specific activity
 
−
cm = addParameter(cm, 'sa', 1); % decay constant
 
−
 
−
 
−
% define the time
 
−
tmin = 0;
 
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tmax = 120;
 
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t = [0:1:tmax]';
 
−
scanTime = [t t+0.01];
 
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cm = set(cm, 'ScanTime', scanTime);
 
−
 
 
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% details needed for MM kinetics link
 
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substrateCompartmentIndex = { 1 };
 
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pName = {'Vm', 'Km'};          % Vm and Vm parameter names
 
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cm = addLink(cm, 'KSpecial', 'Substrate', 'Product', 'Kmm', 'kinMM', pName, substrateCompartmentIndex);
 
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% set initial concentration and TIME
 
−
IC.time = 0;
 
−
IC.compartment = [conc; 0];  % all substrate, no product
 
−
cm = set(cm, 'InitialConditions', IC);
 
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−
% run the model
 
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[cAvg, cAvgIdx, c1, cIdx]  = solve(cm);
 
−
 
 
−
 
−
% repeat experiment with more substrate
 
−
IC.compartment = [4*conc; 0];  % all substrate, no product
 
−
cm = set(cm, 'InitialConditions', IC);
 
−
[cAvg, cAvgIdx, c2, cIdx]  = solve(cm);
 
−
 
−
% plot results
 
−
plot(c1(:,1), c1(:,[2 3]), c2(:,1), c2(:,[2 3]));
 
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legend('Substrate, Exp 1', 'Product, Exp 1', 'Substrate, Exp 2', 'Product, Exp 2')
 
−
 
−
The plot looks like this.
 
−
 
 
−
Model Output Plot
 
−
<br>[[Image:ModelOutputPlot.png]]
 
−
<br>A slightly more elaborate version of this example can be found in comkat\examples\tutorialMichaelisMenten.m
 

Latest revision as of 20:48, 7 August 2012

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