New tools for the rapid analysis of Poliovirus genomic surveillance data
Lead Research Organisation:
Imperial College London
Department Name: School of Public Health
Abstract
This project aims to apply a range of phylogeographic models to quantify the geographic spread
of poliovirus. This analysis aims to produce a protocol which can be implemented downstream
of standard sanger sequencing and next generation sequencing methods being trialled within
the vaccine epidemiology research group and will include tree construction and visualisation
methods.
-To improve on current phylogenetic methods used to infer phylogenies for wild poliovirus
10
in Pakistan and Afghanistan.
- Analyses based on new epidemiological blocks of transmission with genetically
related poliovirus and connected human demography.
- Discrete trait analysis fitting to infer geographic location of internal nodes in the
phylogeny and determine movement of virus between epidemiological blocks.
- Extension of discrete trait methods to quantify the influence of incomplete sampling
on the movement rates inferred.
- Application of coalescent approximations to better understand the influence of
incomplete sampling. This may not be possible on the full data set provided for
endemic countries as the number of states and lineages to be considered is too large.
- To provide visualisations of genetic data for poliovirus with more coherent and relevant
information for policymakers.
- Simple workflow from phylogenetic output to visualisation in R.
- Inclusion of information deemed to be of importance by policymakers.
- Form code in to an R package or code notebook to provide the visualisation
functionality for use on other datasets.
of poliovirus. This analysis aims to produce a protocol which can be implemented downstream
of standard sanger sequencing and next generation sequencing methods being trialled within
the vaccine epidemiology research group and will include tree construction and visualisation
methods.
-To improve on current phylogenetic methods used to infer phylogenies for wild poliovirus
10
in Pakistan and Afghanistan.
- Analyses based on new epidemiological blocks of transmission with genetically
related poliovirus and connected human demography.
- Discrete trait analysis fitting to infer geographic location of internal nodes in the
phylogeny and determine movement of virus between epidemiological blocks.
- Extension of discrete trait methods to quantify the influence of incomplete sampling
on the movement rates inferred.
- Application of coalescent approximations to better understand the influence of
incomplete sampling. This may not be possible on the full data set provided for
endemic countries as the number of states and lineages to be considered is too large.
- To provide visualisations of genetic data for poliovirus with more coherent and relevant
information for policymakers.
- Simple workflow from phylogenetic output to visualisation in R.
- Inclusion of information deemed to be of importance by policymakers.
- Form code in to an R package or code notebook to provide the visualisation
functionality for use on other datasets.
Organisations
People |
ORCID iD |
Nicholas Grassly (Primary Supervisor) | |
David Jorgensen (Student) |
Studentship Projects
Project Reference | Relationship | Related To | Start | End | Student Name |
---|---|---|---|---|---|
EP/N509486/1 | 30/09/2016 | 30/03/2022 | |||
2683235 | Studentship | EP/N509486/1 | 02/01/2019 | 31/10/2022 | David Jorgensen |
EP/R513052/1 | 30/09/2018 | 29/09/2023 | |||
2683235 | Studentship | EP/R513052/1 | 02/01/2019 | 31/10/2022 | David Jorgensen |