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Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking

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  • Miller, Craig R.
  • Van Leuven, James T.
  • Wichman, Holly A.
  • Joyce, Paul

Abstract

Fitness landscapes map genotypes to organismal fitness. Their topographies depend on how mutational effects interact – epistasis – andare important for understanding evolutionary processes such as speciation, the rate of adaptation, the advantage of recombination, and the predictability versus stochasticity of evolution. The growing amount of data has made it possible to better test landscape models empirically. We argue that this endeavor will benefit from the development and use of meaningful basic models against which to compare more complex models. Here we develop statistical and computational methods for fitting fitness data from mutation combinatorial networks to three simple models: additive, multiplicative and stickbreaking. We employ a Bayesian framework for doing model selection. Using simulations, we demonstrate that our methods work and we explore their statistical performance: bias, error, and the power to discriminate among models. We then illustrate our approach and its flexibility by analyzing several previously published datasets. An R-package that implements our methods is available in the CRAN repository under the name Stickbreaker.

Suggested Citation

  • Miller, Craig R. & Van Leuven, James T. & Wichman, Holly A. & Joyce, Paul, 2018. "Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking," Theoretical Population Biology, Elsevier, vol. 122(C), pages 97-109.
  • Handle: RePEc:eee:thpobi:v:122:y:2018:i:c:p:97-109
    DOI: 10.1016/j.tpb.2017.10.006
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    References listed on IDEAS

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    4. Sasha F. Levy & Jamie R. Blundell & Sandeep Venkataram & Dmitri A. Petrov & Daniel S. Fisher & Gavin Sherlock, 2015. "Quantitative evolutionary dynamics using high-resolution lineage tracking," Nature, Nature, vol. 519(7542), pages 181-186, March.
    5. Jeremy R. Dettman & Caroline Sirjusingh & Linda M. Kohn & James B. Anderson, 2007. "Incipient speciation by divergent adaptation and antagonistic epistasis in yeast," Nature, Nature, vol. 447(7144), pages 585-588, May.
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    Cited by:

    1. Patrick Mellacher, 2022. "Endogenous viral mutations, evolutionary selection, and containment policy design," Journal of Economic Interaction and Coordination, Springer;Society for Economic Science with Heterogeneous Interacting Agents, vol. 17(3), pages 801-825, July.

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