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PyRoss is a numerical library that offers an integrated platform for inference, forecasts and non-pharmaceutical interventions in structured epidemiological compartment models.
Compartment models of arbitrary complexity can be user-defined through Python dictionaries. The most common epidemiological models, and several less common ones, come pre-defined with the library. Models can include stages to allow for non-exponentially distributed compartmental residence times. Currently, pre-defined models include ones with multiple disease states (exposed, asymptomatic, symptomatic, etc) and may be further divided by age, and by objective medical states (hospitalized, in ICU, etc). The compartment framework supports models for disease surveillance and quarantine and a variety of other processes of epidemiological relevance.
Generative processes can be formulated stochastically (as Markov population processes) or deterministically (as systems of differential equations). Population processes are sampled exactly by the Doob-Gillespie algorithm or approximately by the tau-leaping algorithm while differential equations are integrated by both fixed and adaptive time-stepping. A hybrid algorithm transits dynamically between these depending on the magnitude of the compartmental fluctuations.
Bayesian inference on pre-defined or user-defined models is performed using model-adapted Gaussian processes derived from functional limit theorems for Markov population process. Generative models are fitted to data through the surveillance model allowing for possibily unobserved compartments. The MAP estimates of parameters and their standard errors can be obtained rapidly by optimising, obviating the need for expensive Markov chain Monte Carlo. This enables the fast evaluation of the model evidence, through which competing models may be objectively compared and their forecasts combined by Bayesian model averaging. Forecasts of disease progression, then, can be fully Bayesian, convolving uncertainties in data, parameters and models. The sensitivity of these forecasts is estimated through the Fisher information matrix.
Non-pharmaceutical interventions are implemented as modifications of the contact structures of the model. Optimised control of these structures, given cost functions, is possible.
PyRossGeo is a companion library that supports spatially resolved compartment models with explicit commuting networks.
The libraries are named after Sir Ronald Ross, doctor, mathematician and poet. In 1898 he made "the great discovery" in his laboratory in Calcutta "that malaria is conveyed by the bite of a mosquito". He won the Nobel Prize in 1902 and laid the foundations of the mathematical modelling of infectious diseases.
The library was developed as a part of The Rapid Assistance in Modelling the Pandemic (RAMP) taskforce at the University of Cambridge. In alphabetical order, the authors are: Ronojoy Adhikari, Austen Bolitho, Erik Brorson, Fernando Caballero, Michael Cates, Jakub Dolezal, Tim Ekeh, Jules Guioth, Robert Jack, Julian Kappler, Lukas Kikuchi, Hideki Kobayashi, Irene Li, Joseph Peterson, Patrick Pietzonka, Benjamin Remez, Paul Rohrbach, Rajesh Singh, and Günther Turk. PyRoss development was also partially supported by a Microsoft Research Award for "Building an open platform for pandemic modelling".
Please read the PyRoss paper and PyRoss Wiki before you use PyRoss for your research. Open an issue, in preference to emailing us with queries. Join our Slack channel for discussion. Please follow the Contributor Covenant in all PyRoss fora. Thank you!
You can take PyRoss for a spin without installation: 
This is the recommended way as it downloads a whole suite of examples along with the package.
>> git clone https://github.com/rajeshrinet/pyross.git
>> cd pyross
>> pip install -r requirements.txt
>> python setup.py installInstall PyRoss and an extended list of dependencies, via Anaconda, in an environment named pyross:
>> git clone https://github.com/rajeshrinet/pyross.git
>> cd pyross
>> make env
>> conda activate pyross
>> makeInstall the latest PyPI version
>> pip install pyrossShort test of initialisation and running
>> make testLong test of all example notebooks. Optionally can specify path and recursion to test a certain subset of notebooks
>> make nbtest -e path=examples/deterministic/PyRoss has model-agnostic, formulation-agnostic intuitive interface. Once a model is instantiated, stochastic, deterministic and hybrid simulations can be performed through the same interface. The example below shows how to set up a deterministic SIR simulation with three age-groups.
# SIR with three age-groups (M=3)
import numpy as np
import pyross
import matplotlib.pyplot as plt
model_spec = { "classes" : ["S", "I"],
"S" : {"infection" : [ ["I","S", "-beta"] ]}, ## the I class passes infection to S class
"I" : { "linear" : [ ["I", "-gamma"] ], ## this is recovery process for I class
"infection" : [ ["I", "S", "beta"]]}
## the recovered class R is internally determined by number conservation
}
parameters = {'beta' : 0.1,
'gamma' : 0.1,
}
M=3; Ni=1000*np.ones(M); N=np.sum(Ni)
# Initial conditions as an array
x0 = np.array([
980, 980, 980, # S
20, 20, 20, # I
])
# Or initial conditions as a dictionary
x0 = {'S': [n-20 for n in Ni], 'I': [20, 20, 20] }
CM = np.array( [[1, 0.5, 0.1],
[0.5, 1, 0.5],
[0.1, 0.5, 1 ]], dtype=float)
def contactMatrix(t):
return CM
# duration of simulation and data file
Tf = 160; Nf=Tf+1;
det_model = pyross.deterministic.Model(model_spec, parameters, M, Ni)
# simulate model
data = det_model.simulate(x0, contactMatrix, Tf, Nf)
# plot the data and obtain the epidemic curve
S = np.sum(det_model.model_class_data('S', data), axis=1)
I = np.sum(det_model.model_class_data('I', data), axis=1)
R = np.sum(det_model.model_class_data('R', data), axis=1)
t = data['t']
fig = plt.figure(num=None, figsize=(10, 8), dpi=80, facecolor='w', edgecolor='k')
plt.rcParams.update({'font.size': 22})
plt.fill_between(t, 0, S/N, color="#348ABD", alpha=0.3)
plt.plot(t, S, '-', color="#348ABD", label='$S$', lw=4)
plt.fill_between(t, 0, I/N, color='#A60628', alpha=0.3)
plt.plot(t, I, '-', color='#A60628', label='$I$', lw=4)
plt.fill_between(t, 0, R/N, color="dimgrey", alpha=0.3)
plt.plot(t, R, '-', color="dimgrey", label='$R$', lw=4)
plt.legend(fontsize=26); plt.grid()
plt.autoscale(enable=True, axis='x', tight=True)
plt.ylabel('Compartment value')
plt.xlabel('Days');Read more in the examples folders.
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Bayesian inference across multiple models suggests a strong increase in lethality of COVID-19 in late 2020 in the UK. Patrick Pietzonka, Erik Brorson, William Bankes, Michael E. Cates, Robert L. Jack, R. Adhikari medRxiv, 2021
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Efficient Bayesian inference of fully stochastic epidemiological models with applications to COVID-19. Yuting I. Li, Günther Turk, Paul B. Rohrbach, Patrick Pietzonka, Julian Kappler, Rajesh Singh, Jakub Dolezal, Timothy Ekeh, Lukas Kikuchi, Joseph D. Peterson, Hideki Kobayashi, Michael E. Cates, R. Adhikari, Robert L. Jack, arXiv:2010.11783, 2020 | ResearchGate
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Efficient and flexible methods for time since infection models, Joseph D. Peterson, R. Adhikari, arXiv:2010.10955, 2020
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Inference, prediction and optimization of non-pharmaceutical interventions using compartment models: the PyRoss library. R. Adhikari, Austen Bolitho, Fernando Caballero, Michael E. Cates, Jakub Dolezal, Timothy Ekeh, Jules Guioth, Robert L. Jack, Julian Kappler, Lukas Kikuchi, Hideki Kobayashi, Yuting I. Li, Joseph D. Peterson, Patrick Pietzonka, Benjamin Remez, Paul B. Rohrbach, Rajesh Singh, and Günther Turk, arXiv:2005.09625, 2020 | ResearchGate.
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Age-structured impact of social distancing on the COVID-19 epidemic in India. Rajesh Singh and R. Adhikari, arXiv:2003.12055, 2020 | ResearchGate.
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