Epidemic inverse problems: geometry and sampling
Lead Research Organisation:
University of Warwick
Department Name: Mathematics
Abstract
Imagine an epidemic is doubling in size every six days soon after the first
cases are announced. If you know cases are all infectious for six days then a
back-of-the envelope calculation tells you that each case infects on average a
further three before recovering and vaccine coverage of 67% or greater is
needed to contain the outbreak. But if you don't know anything about how long
people with the disease are contagious for, then this simple calculation cannot
be made without additional information.
This project aims to quantify that uncertainty, so that when a measurement of
the duration of infectiousness is made then we will be able to assess how
infectious the disease associated with a particular outbreak is likely to be.
Also, when you have a cold then it is is convenient to describe your disease
state 'categorically', which is to say that you will say "I'm coming down with
a cold", "I'm in the middle of a cold", or "I'm just getting better from a
cold", rather than "my viral titre is probably 3 on a logarithmic scale". It
is also often convenient for scientific epidemiologists to take a categorical
approach to disease state, and this project proposes to find a reliable method
for deciding what the relevant categories should be.
cases are announced. If you know cases are all infectious for six days then a
back-of-the envelope calculation tells you that each case infects on average a
further three before recovering and vaccine coverage of 67% or greater is
needed to contain the outbreak. But if you don't know anything about how long
people with the disease are contagious for, then this simple calculation cannot
be made without additional information.
This project aims to quantify that uncertainty, so that when a measurement of
the duration of infectiousness is made then we will be able to assess how
infectious the disease associated with a particular outbreak is likely to be.
Also, when you have a cold then it is is convenient to describe your disease
state 'categorically', which is to say that you will say "I'm coming down with
a cold", "I'm in the middle of a cold", or "I'm just getting better from a
cold", rather than "my viral titre is probably 3 on a logarithmic scale". It
is also often convenient for scientific epidemiologists to take a categorical
approach to disease state, and this project proposes to find a reliable method
for deciding what the relevant categories should be.
Planned Impact
The following non-academics have been identified as benificiaries of the
research:
1. The public through enhanced understanding of infectious disease
epidemiology;
2. Non-academic biostatisticians and epidemiologists who will be able to use
the methods developed.
research:
1. The public through enhanced understanding of infectious disease
epidemiology;
2. Non-academic biostatisticians and epidemiologists who will be able to use
the methods developed.
Publications

Ball F
(2016)
Reproduction numbers for epidemic models with households and other social structures II: Comparisons and implications for vaccination.
in Mathematical biosciences

De Angelis D
(2015)
Four key challenges in infectious disease modelling using data from multiple sources.
in Epidemics

Heesterbeek H
(2015)
Modeling infectious disease dynamics in the complex landscape of global health
in Science

House T
(2015)
For principled model fitting in mathematical biology.
in Journal of mathematical biology

House T
(2015)
Testing the hypothesis of preferential attachment in social network formation.
in EPJ data science

House T
(2016)
Bayesian uncertainty quantification for transmissibility of influenza, norovirus and Ebola using information geometry.
in Journal of the Royal Society, Interface

Pellis L
(2015)
Real-time growth rate for general stochastic SIR epidemics on unclustered networks.
in Mathematical biosciences

Pellis L
(2015)
Eight challenges for network epidemic models.
in Epidemics

Pellis L
(2015)
Exact and approximate moment closures for non-Markovian network epidemics.
in Journal of theoretical biology
Description | 1) That we have better models for understanding the dynamics of an epidemic which can use data which repeatedly samples who is shedding virus, in particular influenza (via nasal swab), norovirus (via stool sample) and ebola (via blood titre). Previously analysing this data using our standard models was challenging, and more complex models are less amenable to analysis. In this project we have developed methods to fit standard models using this type of data. (2) That we have better methods for large-scale multiple imputation to inform epidemiological models. This was a particularly challenging, as it is difficult to weight the different data sources correctly, but we have overcome this by developing new methodologies. |
Exploitation Route | This grant has developed two types of findings which can be brought forward. The analysis of respiratory syncytial virus will be used to inform control policy for this potentially deadly disease. In addition, the novel methodologies for analysing the data will inform both other modelling studies and epidemiological study design. |
Sectors | Healthcare |