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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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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 |
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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 |
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