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Decoding the Fundamental Drivers of Phylodynamic Inference
被引:2
|作者:
Featherstone, Leo A.
[1
]
Duchene, Sebastian
[1
]
Vaughan, Timothy G.
[2
,3
]
机构:
[1] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Vic, Australia
[2] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Basel, Switzerland
[3] Swiss Inst Bioinformat, Lausanne, Switzerland
基金:
英国医学研究理事会;
澳大利亚研究理事会;
关键词:
phylodynamics;
birth-death model;
Bayesian phylogenetics;
D O I:
10.1093/molbev/msad132
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Despite its increasing role in the understanding of infectious disease transmission at the applied and theoretical levels, phylodynamics lacks a well-defined notion of ideal data and optimal sampling. We introduce a method to visualize and quantify the relative impact of pathogen genome sequence and sampling times-two fundamental sources of data for phylodynamics under birth-death-sampling models-to understand how each drives phylodynamic inference. Applying our method to simulated data and real-world SARS-CoV-2 and H1N1 Influenza data, we use this insight to elucidate fundamental trade-offs and guidelines for phylodynamic analyses to draw the most from sequence data. Phylodynamics promises to be a staple of future responses to infectious disease threats globally. Continuing research into the inherent requirements and trade-offs of phylodynamic data and inference will help ensure phylodynamic tools are wielded in ever more targeted and efficient ways.
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