DISSEQT—DIStribution-based modeling of SEQuence space Time dynamics†

Author:

Henningsson R1234,Moratorio G25,Bordería A V3,Vignuzzi M2,Fontes M3678

Affiliation:

1. The Centre for Mathematical Sciences, Lund University, Sweden

2. Viral Populations and Pathogenesis Unit, Institut Pasteur, Paris, France

3. The International Group for Data Analysis, Institut Pasteur, Paris, France

4. Division of Clinical Genetics, Lund University, Sweden

5. Laboratorio de Virología Molecular, Universidad de la República, Montevideo, Uruguay

6. Department of Cancer Immunology, Genentech, South San Francisco, CA, USA

7. The Center for Genomic Medicine, Rigshospitalet, Copenhagen, Denmark

8. Persimune, The Centre of Excellence for Personalized Medicine, Copenhagen, Denmark

Abstract

Abstract Rapidly evolving microbes are a challenge to model because of the volatile, complex, and dynamic nature of their populations. We developed the DISSEQT pipeline (DIStribution-based SEQuence space Time dynamics) for analyzing, visualizing, and predicting the evolution of heterogeneous biological populations in multidimensional genetic space, suited for population-based modeling of deep sequencing and high-throughput data. The pipeline is openly available on GitHub (https://github.com/rasmushenningsson/DISSEQT.jl, accessed 23 June 2019) and Synapse (https://www.synapse.org/#!Synapse: syn11425758, accessed 23 June 2019), covering the entire workflow from read alignment to visualization of results. Our pipeline is centered around robust dimension and model reduction algorithms for analysis of genotypic data with additional capabilities for including phenotypic features to explore dynamic genotype–phenotype maps. We illustrate its utility and capacity with examples from evolving RNA virus populations, which present one of the highest degrees of genetic heterogeneity within a given population found in nature. Using our pipeline, we empirically reconstruct the evolutionary trajectories of evolving populations in sequence space and genotype–phenotype fitness landscapes. We show that while sequence space is vastly multidimensional, the relevant genetic space of evolving microbial populations is of intrinsically low dimension. In addition, evolutionary trajectories of these populations can be faithfully monitored to identify the key minority genotypes contributing most to evolution. Finally, we show that empirical fitness landscapes, when reconstructed to include minority variants, can predict phenotype from genotype with high accuracy.

Funder

Defense Advanced Research Projects Agency

DARPA

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

Reference50 articles.

1. Mutational and Fitness Landscapes of an RNA Virus Revealed through Population Sequencing;Acevedo;Nature,2014

2. Design and Computational Analysis of Single-Cell RNA-Sequencing Experiments;Bacher;Genome Biology,2016

3. Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency;Beaucourt;Journal of Visualized Experiments,2011

4. Challenges and Opportunities in Estimating Viral Genetic Diversity from Next-Generation Sequencing Data;Beerenwinkel;Frontiers in Microbiology,2012

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