This course is meant to provide students in applied mathematics with the broad skill-set needed to optimize model parameters to relevant biological or epidemic data. The course will almost entirely be based on material posted on this website. Continue reading →
The file hare_lynx.txt contains data on the number of arctic hare and lynx pelts collected by the Hudson’s Bay company in Canada over the course of many years (data obtained from this website). Do you think the Lotka-Volterra model is an appropriate model to fit to these data?
ASU students in the spring semester of AML610 should have already applied for and received an account on the Saguaro system (per the instructions of last month’s email describing how to apply for an account).
Saguaro allows you to simultaneously run multiple jobs in batch, directing standard output to a log file. For this course, we will be using Saguaro to solve a system of ODE’s under a hypothesis for the parameters and initial conditions values (either chosen in a parameter sweep, or randomly chosen within some range); the output of the ODE’s will then be compared to a data set, and a best-fit statistic (like Least Squares, Pearson chi-squared, or Maximum likelihood) computed. The parameter values and best-fit statistics are then printed to standard output.
Access to cloud computing resources, and knowledge of how to utilize those resources, has many different potential applications in modelling. Learning how to use Saguaro as a tool in solving problems related to this course can thus potentially open up many further avenues of future research to you.
Homework #5, due Thus April 18th, 2013 at 6pm. Data for the homework can be found here.
Some (potentially) useful utilities for random number generation and manipulating vectors in C++
I’ve written some C++ code mainly related to vectors; calculating the weighted mean, running sum, extracting every nth element, etc). There are also utilities related to random number generation from various probability distributions, and methods to calculate the CDF of various probability distributions.
The file UsefulUtils.h and UsefulUtils.cpp contain source code of a class that contains these utilities that can be useful when performing compartmental modelling in C++. These utilities will be used extensively in the examples that will be presented in this, and later, modules. The file example_useful_utils.cpp gives examples of the use of the class. It can be compiled with the makefile makefile_use with the command
make -f makefile_use example_useful_utils
Homework #4, due April 3rd, 2013 at 6pm. The data for the homework can be found here.
After going through this module, students will be familiar with the Euler and Runge-Kutta methods for numerical solution of systems of ordinary differential equations. Examples are provided to show students how complementary R scripts can be written to help debug Runge-Kutta methods implemented in C++.
After going through this module, students should be familiar with basic skills in C++ programming, including the structure of a basic program, variable types, scope, functions (and function overloading), control structures, and the standard template library.
So far in this course we have used R to explore methods related to fitting model parameters to data (in particular, we explored the Simplex method for parameter estimation). As we’ve shown, parameter estimation can be a very computationally intensive process.
When you use R, it gives you a prompt, and waits for you to input commands, either directly through the command line, or through an R script that you source. Because R is a non-compiled language, and instead interprets code step-by-step, it does not have the ability to optimize calculations by pre-processing the code.
In contrast, compiled programming languages like C, java, or C++ (to name just a few) use a compiler to process the code, and optimize the computational algorithms. In fact, most compilers have optional arguments related to the level of optimization you desire (with the downside that the optimization process can be computationally intensive). Optimized code runs faster than non-optimized code.
In this module students will compare the performance of several fitting methods (Least squares, Pearson chi-squared, and likelihood fitting methods) in estimating the rate of exponential rise in initial epidemic incidence data. Students will learn about the properties of good estimators (bias and efficiency).
[After reading this module, students should understand the Least Squares goodness-of-fit statistic. Students will be able to read an influenza data set from a comma delimited file into R, and understand the basic steps involved in the graphical Monte Carlo method to fit an SIR model to the data to estimate the R0 of the influenza strain by minimizing the Least Squares statistic. Students will be aware that parameter estimates have uncertainties associated with them due to stochasticity (randomness) in the data.]
When a new virus starts circulating in the population, one of the first questions that epidemiologists and public health officials want answered is the value of the reproduction number of the spread of the disease in the population (see, for instance, here and here).
The length of the infectious period can roughly be estimated from observational studies of infected people, but the reproduction number can only be estimated by examination of the spread of the disease in the population. When early data in an epidemic is being used to estimate the reproduction number, I usually refer to this as “real-time” parameter estimation (ie; the epidemic is still ongoing at the time of estimation).
[After reading this module, students should be familiar with probability distributions most important to modelling in the life and social sciences; Uniform, Normal, Poisson, Exponential, Gamma, Negative Binomial, and Binomial.]
There are various probability distributions that are important to be familiar with if one wants to model the spread of disease or biological populations (especially with stochastic models). In addition, a good understanding of these various probability distributions is needed if one wants to fit model parameters to data, because the data always have underlying stochasticity, and that stochasticity feeds into uncertainties in the model parameters. It is important to understand what kind of probability distributions typically underlie the stochasticity in epidemic or biological data. Continue reading →
In the Arizona State University AML610 course “Computational and Statistical Methods in Applied Mathematics”, we will be ultimately be using super computing resources at ASU and the NSF XSEDE initiative to fit the parameters of a biological model to data. To do this, it is necessary to know basic Unix commands to copy, rename, and delete files and directories, and how to list directories and locate files. We will also be compiling all our C++ programs from the Unix shell, and in the command line directing the output of our programs to files. Continue reading →
[After going through this module, students will be familiar with time-dependent transmission rates in a compartmental SIR model, will have explored some of the complex dynamics that can be created when the transmission is not constant, and will understand applications to the modelling of influenza pandemics.]
Influenza is a seasonal disease in temperate climates, usually peaking in the winter. This implies that the transmission of influenza is greater in the winter (whether this is due to increased crowding and higher contact rates in winter, and/or due to higher transmissibility of the virus due to favorable environmental conditions in the winter is still being discussed in the literature). What is very interesting about influenza is that sometimes summer epidemic waves can be seen with pandemic strains (followed by a larger autumn wave). An SIR model with a constant transmission rate simply cannot replicate the annual dual wave nature of an influenza pandemic.
[After reading through this module, students should have an understanding of contact dynamics in a population with age structure (eg; kids and adults). You should understand how population age structure can affect the spread of infectious disease. You should be able to write down the differential equations of a simple SIR disease model with age structure, and you will learn in this module how to solve those differential equations in R to obtain the model estimate of the epidemic curve]
In a previous module I discussed epidemic modelling with a simple Susceptible, Infected, Recovered (SIR) compartmental model. The model presented had only a single age class (ie; it was homogenous with respect to age). But in reality, when we consider disease transmission, age likely does matter because kids usually make more contacts during the day than adults. The differences in contact patterns between age groups can have quite a profound impact on the model estimate of the epidemic curve, and also have implications for development of optimal disease intervention strategies (like age-targeted vaccination, social distancing, or closing schools). Continue reading →
[After reading through this module you should have an intuitive understanding of how infectious disease spreads in the population, and how that process can be described using a compartmental model with flow between the compartments. You should be able to write down the differential equations of a simple disease model, and you will learn in this module how to numerically solve those differential equations in R to obtain the model estimate of the epidemic curve]
Models of disease spread can yield insights into the mechanisms and dynamics most important to the spread of disease (especially when the models are compared to epidemic data). With this improved understanding, more effective disease intervention strategies can potentially be developed. Sometimes disease models are also used to forecast the course of an epidemic, and doing exactly that for the 2009 pandemic was my introduction to the field of computational epidemiology.
There are lots of different ways to model epidemics, and there are several modules on this site on the topic, but let’s begin with one of the simplest epidemic models for an infectious disease like influenza: the Susceptible, Infected, Recovered (SIR) model.
[After you have read through this module, and have downloaded and worked through the provided R examples, you should be proficient enough in R to be able to download and run other R scripts that will be provided in other posts on this site. You should understand the basics of good programming practices (in any language, not just R). You will also have learned how to read data in a file into a table in R, and produce a plot.]
I have programmed in many different computing and scripting languages, but the ones I most commonly use on a day to day basis are C++, Fortran, Perl, and R (with some Python, Java, and Ruby on the side). In particular, I use R every day because it is not only a programming language, but also has graphics and a very large suite of statistical tools. Connecting models to data is a process that requires statistical tools, and R provides those tools, plus a lot more.
Unlike SAS, Stata, SPSS, and Matlab, R is free and open source (it is hard to beat a package that is more comprehensive than pretty much any other product out there and is free!).
[In this module we discuss methods for finding free sources of online data. We present examples of climate, population, and socio-economic data from a variety of online sources. Other sources of potentially useful data are also discussed. The data sources described here are by no means an exhaustive list of free online data that might be useful to use in a computational, statistical, or mathematical modeling study.]Continue reading →
Connecting mathematical models to predicting reality usually involves comparing your model to data, and finding model parameters that make the model most closely match observations in data. And of course statistical models are wholly developed using sources of data.
Becoming adept at finding sources of data relevant to a model you are studying is a learned skill, but unfortunately one that isn’t taught in any textbook!
One thing to keep in mind is that any data that appears in a journal publication is fair game to use, even if it appears in graphical format only. If the data is in graphical format, there are freeprograms, such as DataThief, that can be used to extract the data into a numerical file.
Google Scholar is search engine that indexes the scholarly literature across an array of publishing formats and disciplines. It provides a very powerful means to find literature associated with pretty much any research topic you can think of.
The final write-ups for final group projects are due Monday, December 1st, 2014. On Dec 2nd and 3rd students will meet with Prof Towers to receive feedback on their project and writeup.
Each of the project groups will perform an in-class 20 min presentation on Monday, Dec 8th, 2014 and Wed, Dec 10th, 2014. By Dec 9th, all group members are to submit to Prof Towers a confidential email, detailing their contribution to the group project, and detailing the contributions of the other group members.
The list of modules for the Fall 2014 course in computational and statistical methods for mathematical biologists and epidemiologists: