Gradients Do Grow on Trees: A Linear-Time O(N)-Dimensional Gradient for Statistical Phylogenetics

Author:

Ji Xiang12ORCID,Zhang Zhenyu3,Holbrook Andrew3,Nishimura Akihiko4,Baele Guy5,Rambaut Andrew6,Lemey Philippe5,Suchard Marc A137

Affiliation:

1. Department of Biomathematics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA

2. Department of Mathematics, School of Science & Engineering, Tulane University, New Orleans, LA

3. Department of Biostatistics, Fielding School of Public Health, University of California Los Angeles, Los Angeles, CA

4. Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD

5. Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium

6. Institute of Evolutionary Biology, Centre for Immunology, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom

7. Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA

Abstract

Abstract Calculation of the log-likelihood stands as the computational bottleneck for many statistical phylogenetic algorithms. Even worse is its gradient evaluation, often used to target regions of high probability. Order O(N)-dimensional gradient calculations based on the standard pruning algorithm require O(N2) operations, where N is the number of sampled molecular sequences. With the advent of high-throughput sequencing, recent phylogenetic studies have analyzed hundreds to thousands of sequences, with an apparent trend toward even larger data sets as a result of advancing technology. Such large-scale analyses challenge phylogenetic reconstruction by requiring inference on larger sets of process parameters to model the increasing data heterogeneity. To make these analyses tractable, we present a linear-time algorithm for O(N)-dimensional gradient evaluation and apply it to general continuous-time Markov processes of sequence substitution on a phylogenetic tree without a need to assume either stationarity or reversibility. We apply this approach to learn the branch-specific evolutionary rates of three pathogenic viruses: West Nile virus, Dengue virus, and Lassa virus. Our proposed algorithm significantly improves inference efficiency with a 126- to 234-fold increase in maximum-likelihood optimization and a 16- to 33-fold computational performance increase in a Bayesian framework.

Funder

European Research Council under the European Union’s Horizon 2020

Wellcome Trust

NSF

NIH-NIAID

Interne Fondsen KU Leuven/Internal Funds KU Leuven

Research Foundation—Flanders

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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