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Title: Simulation: Software Methods and Biological Processes


1
SimulationSoftware Methods and Biological
Processes
  • Marco AntoniottiNYU Courant Bioinformatics Group

2
Outline
  • Simulation fundamentals
  • Modeling
  • Modeling Tools
  • Mathematical Tools (Differential Equations, Timed
    Systems)
  • Languages
  • Software infrastructure and implementations
  • Models of computations
  • Numerics

3
Outline (continued)
  • Tools
  • General
  • Matlab, Mathematica, Maple, Macsyma
  • Specialized
  • Discrete Event with Extensions
  • Hybrid System Simulators
  • Biological Simulations
  • E-CELL, VirtualCell

4
Modeling
  • There are several frameworks that can be used for
    modeling
  • Differential Equations (continuous)
  • Discrete Systems
  • Finite State Automata
  • Petri Nets
  • Dataflow Diagrams

5
Time
  • The main issue behind all of these modeling
    frameworks is Time
  • Consequences
  • What constitues progress
  • How do we implement simulators for systems that
    assume a different notion of time'

6
Differential Equations
  • Ordinary Differential Equations (ODE's) are a
    standard tool used to model physical, biological
    and engineering systems y'(t) F(y(t),
    t) y(0) k
  • Time t is continuous'

7
Discrete Models
  • Finite State Machines
  • Petri Nets
  • Discrete Event Systems
  • A queue of events' generated by some sources'
    and processed by components'
  • Time is a usually a derived notion (e.g. by
    observing the sequence of events or a Wall Clock)

8
ODE Repressilator System
  • The repressilator system (Elowizt, Leibler 2000)
    comprises three proteins, LacI, CI, and TetR
    controlling each other.

TetR
CI
LacI
9
ODE Repressilator System
  • The repressilator system (Elowizt, Leibler 2000)
    is simply described as an ODE system
    (deterministic version)(i,j) (lacI,cI) or
    (tetR,lacI) or (cI,tetR)

10
Stem Cell Population Model
  • There are different kinds of (Adult) Stem Cells
  • Hematopoietic, Neuronal, Muscle, Epithelial
  • A Stem Cell differentiates into Committed
    Progenitor Cells, which in turn differentiate
    into Regular Cells (T-cells, Red Blood Cells,
    Skin Cells)

11
Stem Cell Differentiation and Proliferation
  • Stem Cell Division/Proliferation
  • Asymmetric
  • Symmetric
  • Environmentally Asymmetric

12
Stem Cell FSA
Asymmetric Division
Ns n. of Stem Cells Np n. of Progenitor Cells
Np Np 1
Ns Ns -1
Symmetric Division 2S
die
quiescent
Ns Ns 1
Np Np 2 Ns Ns -1
SymmetricDivision 2P
13
Stem Cells Population ODE Model
14
Simulation Traces
  • Running a simulation (numerically solving a set
    of differential equations) produces a trace
  • A trace is a sequence of vectors of values,
    possibly symbolic
  • E.g. for the FSA Stem Cell Model we havelt(100,
    1e5), (101, 1e5), ... (98, 1e5)gt

15
Discrete Event Systems
  • The notion of trace gives rise to a more low
    level notion of system.
  • Discrete Event Simulators are defined in terms of
    the underlying timed traces and of their
    generators

16
Simulator Template Architecture
System Specification
Simulation Results (Traces)
Trace Inspection Synchronous GUI Plotter Math
Analysis
Simulation Engine
17
Implementing a Simulator
  • The engine of a simulator is essentially a
    loop loop for i from start to finish do
    (evaluate next(i))
  • The nature of (evaluate next(i)) determines the
    type of simulator we are using

18
Simulator Runtime
  • The simulator runtime can be
  • stopped
  • when stopped, one or more individual components
    can be instantiated (or retrieved) and activated
  • restarted
  • when restarted, the simulation will proceed with
    the individual components behaving as if part of
    the overall simulation (this may be considered as
    a lens effect)

19
Implementing a Discrete Event Simulator
  • SpecificationSources, Computing Units and Sinks
  • Sources square wave generators
  • Units down samplers, logical operation
  • Engine
  • A queue of pairs lttime, valuegt
  • Evaluators for the units
  • Each unit can sense if it has inputs

20
Implementing a FSA Simulator
  • Specification
  • A set of Finite Automata
  • Two possibilities
  • Construct a product automata and then simulate
  • Keep Automata separate and make simulation
    slightly more complex
  • Engine
  • check the set of all enabled transitions from the
    current state and produce the next state

21
Implementing an ODE Simulator/Solver
  • Specification
  • A set of ODE's
  • Engine
  • Evaluate at discrete time steps the value of the
    function and of its derivative
  • Several different methods are available
  • Euler
  • Runke-Kutta

22
Implementing an ODE Simulator/Solver (contd)
  • Euler Method (unrecommended)
  • Runge-Kutta 4

23
Implementing an ODE Simulator (contd.)
  • Complete formulation of midpoint computations in
    Runge-Kutta 4

24
Stem Cell Population Octave (Matlab) Code
  • The ODE formulation isfunction dn f(N,
    t) alphap 0.01 alphas 0.01 beta 5
    gamma 0.2 theta 0.2 kappa 0.5 Ks
    1000 Kp 10000 dn(1) (beta (Ks -
    N(1))/Ks - theta (Kp - N(2))/Kp - alphas)
    N(1) dn(2) (Kp - N(2))/Kp ((gamma 2
    theta) N(1) kappa N(2))
    - alphap N(2)endfunctionN0
    50 1000 t linspace(0, 15, 100)'N
    lsode("f", N0, t)

25
Running the code
26
A Finite Automata LanguageEsterel
  • Consider the following example

?B
?A
?R
?R
?A?B!O
?R
?B!O
?A!O
27
Esterel Rendition
  • The previous automata is rendered as module
    ABRO input A, B output O loop await A
    await B emit O each R end
  • Each transition happens at each tick

28
Putting it all together
  • How do we reconcile a high level modeling view
    with a low level continuous time based
    simulation?
  • Hybrid Systems are one of the latest developments
    mixing Finite State Automata and Continuous
    Systems

29
Hybrid Systems
  • A Hybrid System is a computational tool that
    switches among different sets of ODE's accoding
    to a some conditions

k1 gt k2
y gt k1
dy/dt 3
dy/dt -1.5
y lt k2
30
A Hybrid System Implementation
  • The main loop of a Hybrid System simulation
    engine becomeslet h ltsome valuegtloop for i
    from start to finish do evaluate the current set
    of ODE's for one step h if (any transition
    becomes enabled) do switch ODE set

31
Stem Cells PopulationHybrid System Formulation
  • The Stem Cell ODE formulation is a deterministic
    and continuous approximation of the real (?!?)
    model
  • An Hybrid System formulation can be made closer
    to the discrete and stochastic counting nature of
    the model

32
Stem Cells PopulationHybrid System (contd)
  • We model the Stem Cell Population as a Hybrid
    System with only one differential (continuous)
    variable time (time)
  • Our system will therefore integrate d time / dt
    1

33
Stem Cells PopulationHybrid System (contd)
  • We associate to each transition an exponential
    decay rate
  • The exponential decay rate represents the rate'
    of an event in the population model (asymmetric
    division, apoptosis)

quiescent
Ns Ns -1
d(time)/dt 1r(die) random()
die
- ln(r(die)) lt alpha Ns time
34
Stem Cells PopulationHybrid System (contd)
  • One language that can be used to this end is
    l-Shift (Simsek 2000, UC Berkeley)(defhybrid
    SC-behavior () ... (discrete
    ('quiescent flow ((d/dt time)

    (random 1.0)))) (transitions ('quiescent 'die
    when (lt (- (log r) ( alpha n_s time)))
    do ((time 0)
    (n_s
    (decf n_s)))) ))

35
Problems with HS
  • There are several Numerical problems
  • Guard Crossings

36
Conclusions
  • Simulations are a good tool for Modeling several
    systems, hence Biological Systems as well
  • We saw different kinds of simulation paradigms
  • continous
  • discrete
  • hybrid

37
Conclusions (2)
  • A simulation tool must be fitted to the problem
    at hand
  • Proper modeling is always a prerequisite to
    produce data that can be analyzed by matching it
    with laboratory experimental results

38
The ModelCell Differentiation
  • Cell Differention (e.g. multipotent HSCs,
    Metcalfe et al. 1997)

M
V
G2
G1
R
C
S
G0
Apoptosis
39
The ModelCell Differentiation
  • Cell Differention (e.g. multipotent HSCs,
    Metcalfe et al. 1997)

Macrophages
GM-Progenitors
Granulocytes
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