Cargando…

Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies

Phylogenetic dating is one of the most powerful and commonly used methods of drawing epidemiological interpretations from pathogen genomic data. Building such trees requires considering a molecular clock model which represents the rate at which substitutions accumulate on genomes. When the molecular...

Descripción completa

Detalles Bibliográficos
Autores principales: Didelot, Xavier, Siveroni, Igor, Volz, Erik M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480190/
https://www.ncbi.nlm.nih.gov/pubmed/32722797
http://dx.doi.org/10.1093/molbev/msaa193
_version_ 1784576419363291136
author Didelot, Xavier
Siveroni, Igor
Volz, Erik M
author_facet Didelot, Xavier
Siveroni, Igor
Volz, Erik M
author_sort Didelot, Xavier
collection PubMed
description Phylogenetic dating is one of the most powerful and commonly used methods of drawing epidemiological interpretations from pathogen genomic data. Building such trees requires considering a molecular clock model which represents the rate at which substitutions accumulate on genomes. When the molecular clock rate is constant throughout the tree then the clock is said to be strict, but this is often not an acceptable assumption. Alternatively, relaxed clock models consider variations in the clock rate, often based on a distribution of rates for each branch. However, we show here that the distributions of rates across branches in commonly used relaxed clock models are incompatible with the biological expectation that the sum of the numbers of substitutions on two neighboring branches should be distributed as the substitution number on a single branch of equivalent length. We call this expectation the additivity property. We further show how assumptions of commonly used relaxed clock models can lead to estimates of evolutionary rates and dates with low precision and biased confidence intervals. We therefore propose a new additive relaxed clock model where the additivity property is satisfied. We illustrate the use of our new additive relaxed clock model on a range of simulated and real data sets, and we show that using this new model leads to more accurate estimates of mean evolutionary rates and ancestral dates.
format Online
Article
Text
id pubmed-8480190
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-84801902021-09-30 Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies Didelot, Xavier Siveroni, Igor Volz, Erik M Mol Biol Evol Methods Phylogenetic dating is one of the most powerful and commonly used methods of drawing epidemiological interpretations from pathogen genomic data. Building such trees requires considering a molecular clock model which represents the rate at which substitutions accumulate on genomes. When the molecular clock rate is constant throughout the tree then the clock is said to be strict, but this is often not an acceptable assumption. Alternatively, relaxed clock models consider variations in the clock rate, often based on a distribution of rates for each branch. However, we show here that the distributions of rates across branches in commonly used relaxed clock models are incompatible with the biological expectation that the sum of the numbers of substitutions on two neighboring branches should be distributed as the substitution number on a single branch of equivalent length. We call this expectation the additivity property. We further show how assumptions of commonly used relaxed clock models can lead to estimates of evolutionary rates and dates with low precision and biased confidence intervals. We therefore propose a new additive relaxed clock model where the additivity property is satisfied. We illustrate the use of our new additive relaxed clock model on a range of simulated and real data sets, and we show that using this new model leads to more accurate estimates of mean evolutionary rates and ancestral dates. Oxford University Press 2020-07-28 /pmc/articles/PMC8480190/ /pubmed/32722797 http://dx.doi.org/10.1093/molbev/msaa193 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods
Didelot, Xavier
Siveroni, Igor
Volz, Erik M
Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title_full Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title_fullStr Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title_full_unstemmed Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title_short Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
title_sort additive uncorrelated relaxed clock models for the dating of genomic epidemiology phylogenies
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480190/
https://www.ncbi.nlm.nih.gov/pubmed/32722797
http://dx.doi.org/10.1093/molbev/msaa193
work_keys_str_mv AT didelotxavier additiveuncorrelatedrelaxedclockmodelsforthedatingofgenomicepidemiologyphylogenies
AT siveroniigor additiveuncorrelatedrelaxedclockmodelsforthedatingofgenomicepidemiologyphylogenies
AT volzerikm additiveuncorrelatedrelaxedclockmodelsforthedatingofgenomicepidemiologyphylogenies