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phdthesis's Introduction

Tim CD Lucas

I am a lecturer in the Dept. of Health Sciences at the University of Leicester. My interests encompass statistical methods and mathematical models for studying disease. In particular I’m interested in studying methods that account for multiple temporal or spatial scales. For example, disease progression or diagnosis is typically quite a slow process, but we are exposed to environmental factors such as air pollution every second. Depending on our movement patterns, we can have very different exposures from one minute to the next.

I have a continuing interest in infectious disease models and statistical methods for ecology. Recently this has involved developing models of contact tracing to help guide COVID-19 policy. Previously, I worked as a Research Fellow at Imperial College. Before that I worked with Deirdre Hollingsworth and the Malaria Atlas Project at the Big Data Institute, University of Oxford on neglected tropical diseases and malaria.

Please feel free to email me to discuss stats, modelling, R or anything else. If you are a student looking for opportunities such as masters or PhD projects please email to say hello. There are studentships or pre-doctoral fellowships we could develop a project for. My address is tim.lucas — at — le.ac.uk. Or you can say hello on twitter @timcdlucas or @StatsForBios.

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phdthesis's Issues

Group size vs population structure

There's more lit on group size that I should discuss and discuss why group size and population structure are not the same.

tag +social in jabref

Extra refs

vogwill2009dispersal: our findings suggest that dispersal and natural enemies can interact to drive spatially synchronous population fluctuations that decrease stability

Mechanisms and global change

Depending on the mechanism by which structure affects richness, global change might predict increased richness in the majority of species. Or more new pathogens. Or more virulent paths.

Useful for intro to +ch2.

See discussion of ch3.

Rabies paper

Bioecological Drivers of Rabies Virus Circulation in a Neotropical Bat Community

Cross species: "Positive animals were recorded in 14 out of the 30 species analysed"
monospecific colonies favoured infection?

"the high number of apparently healthy and seropositive bats indicates that, at least in a large number of cases, the clinical expression of the virus, if any, is undetectable"

More actual discussion of reuslts

WHY do I think there was no effect.

\subsubsection{Dispersal does not affect pathogen richness}

Irrespective of the network topology used, at very high dispersal rates a population will be well mixed.

\subsubsection{Network connectedness does not affect pathogen richness}

This is in direct contrast to \cite{campos2006pathogen}.
However, the model in \cite{campos2006pathogen} is a contact network, so increasing the connectedness increases the chance of succesful transmission events for the first few transmission generations.
This lends support to the idea that I found no affect of connectedness due to the dominance of local dynamics.

Is not enough.

Stuff to sort

Reinclude line explain why distrRange is worse than random. Wasn't working with rinline.

On average (mean
weighted by Akaiki weights) there is a negative relationship between gene flow and
viral richness (β = − 0.27, variance = 0.06) despite the apparent positive relationship
in Figure 3.

Add the actual bivariate result for this.

Virus taxonomy

Need to use a proper virus taxonomy.
With a definition of virus species

mass is negative!

FSst anaylsis gives negative coefficient for mass. Needs discussing.

fstmtDNA conversion function

fstmtDNA <- fstallozyme <- function(fst){
  Nm <- 0.5 * (1 / fst - 1)
}

At the moment this is just a guess. I haven't really seen fst mtDNA equations. Bit confused.

All mammals for population structure intro

Do all mammals for Chapter 3 general intro (previous studies). State that I am looking at mammals. Later state that my analysis is on bats (and mention that it's all bats that I could find data for.)

I had a brief look and didn't find many others.

Do I want to include group size?

Density vs abundance

Active debate in disease ecology centers on which measure is preferable for species with various social systems or for different scales of measurement, and on the consequences for modeling disease transmission 16, 17, 18, 19, 20 and 21;

A clarification of transmission terms in host-microparasite models: numbers, densities and areas
How does transmission of infection depend on population size?
A generalized model of parasitoid, venereal and vector-based transmission processes
Modelling transmission: mass action and beyond

Issues in Burns

Miniopterus natalensis: can't match 0.241 value to anything in paper (not mean of pairwise.)
This is from miller2003strong

There's another Miniopterus natalensis record, so ignore.

Randomly seeded colonies.

In each simulation the population was seeded with 10 sets of 200 infected indi-
viduals of disease 1. There groups were seeded into randomly selected colonies with
replacement.

Don't think randomly selected anymore.

Useful refs

Not out but worth watching out for.

Colizza dog paper
Colizza bat paper

Olival. Richness does predict zoonotic potential.

Fig 5.5 colours

More work I did that I lost. Probably can find.

Colours in fig 5.5 need to match 5.4 and 5.6

Variance of coeficients

Currently simply calculating variance of coefficients. But I think a lot of models are identical (i.e. without bootstrapped var.) How should I deal with this?

Bat clocks rocks missing species

Both nSpecies and fst analyses have species not in the bat clocks rocks phylogeny.

For now I am only using species in the phylogeny for nSpecies and will manually add species for fst. The species are all in genera that are represented in the three, so I will make these polytomys I guess.

Bat viruses long lasting

to directly estimate infection durations in wild populations. But it seems that these
infections might be long lasting ().

Check all p values

Check particularly p values but also other values for 10^-50 type silly numbers.

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