Maximum likelihood pandemic-scale phylogenetics

Summary

Phylogenetics plays a crucial role in the interpretation of genomic data¹. Phylogenetic analyses of SARS-CoV-2 genomes have allowed the detailed study of the virus’s origins², of its international^3,4 and local^4–9 spread, and of the emergence¹⁰ and reproductive success¹¹ of new variants, among many applications. These analyses have been enabled by the unparalleled volumes of genome sequence data generated and employed to study and help contain the pandemic¹². However, preferred model-based phylogenetic approaches including maximum likelihood and Bayesian methods, mostly based on Felsenstein’s ‘pruning’ algorithm^13,14, cannot scale to the size of the datasets from the current pandemic^4,15, hampering our understanding of the virus’s evolution and transmission¹⁶. We present new approaches, based on reworking Felsenstein’s algorithm, for likelihood-based phylogenetic analysis of epidemiological genomic datasets at unprecedented scales. We exploit near-certainty regarding ancestral genomes, and the similarities between closely related and densely sampled genomes, to greatly reduce computational demands for memory and time. Combined with new methods for searching amongst candidate evolutionary trees, this results in our MAPLE (‘MAximum Parsimonious Likelihood Estimation’) software giving better results than popular approaches such as FastTree 2¹⁷, IQ-TREE 2¹⁸, RAxML-NG¹⁹ and UShER¹⁵. Our approach therefore allows complex and accurate proba-bilistic phylogenetic analyses of millions of microbial genomes, extending the reach of genomic epidemiology. Future epidemiological datasets are likely to be even larger than those currently associated with COVID-19, and other disciplines such as metagenomics and biodiversity science are also generating huge numbers of genome sequences^20–22. Our methods will permit continued use of preferred likelihood-based phylogenetic analyses.