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The discernible and hidden effects of clonality on the genotypic and genetic states of populations: improving our estimation of clonal ratesuse asterix (*) to get italics
Solenn Stoeckel, Barbara Porro, Sophie Arnaud-HaondPlease use the format "First name initials family name" as in "Marie S. Curie, Niels H. D. Bohr, Albert Einstein, John R. R. Tolkien, Donna T. Strickland"
2019
<p>Partial clonality is widespread across the tree of life, but most population genetics models are conceived for exclusively clonal or sexual organisms. This gap hampers our understanding of the influence of clonality on evolutionary trajectories and the interpretation of population genetics data. We performed forward simulations of diploid populations at increasing rates of clonality (c), analysed their relationships with genotypic and genetic indices, and tested predictions of c from population genetics data through supervised machine learning. Two complementary behaviours emerged from the probability distributions of genotypic and genetic indices with increasing c. While the impact of c on genotypic descriptors (R and β) was easily described by simple mathematical equations, its effects on genetic indices (FIS and linkage disequilibrium) were noticeable only at the highest levels (c&gt;0.95). Consequently, genotypic richness allowed reliable estimates of c, while genetic descriptors led to poorer performances when c&lt;0.95. These results provide clear baseline expectations for genotypic and genetic diversities and dynamics under partial clonality. Worryingly, however, the use of realistic sample sizes to acquire empirical data systematically led to gross underestimates (often of one to two orders of magnitude) of c, calling for a reappraisal of many interpretations hitherto proposed in the literature, mostly based on genotypic richness. We propose future avenues through which to derive realistic confidence intervals for c and show that, although still approximate, a supervised learning method would greatly improve the estimation of c from population genetics data.</p>
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rates of clonality, population genetics, genotypic diversity, F-statistics, sampling
NonePlease indicate the methods that may require specialised expertise during the peer review process (use a comma to separate various required expertises).
Population Genetics / Genomics, Reproduction and Sex
No need for them to be recommenders of PCIEvolBiol. Please do not suggest reviewers for whom there might be a conflict of interest. Reviewers are not allowed to review preprints written by close colleagues (with whom they have published in the last four years, with whom they have received joint funding in the last four years, or with whom they are currently writing a manuscript, or submitting a grant proposal), or by family members, friends, or anyone for whom bias might affect the nature of the review - see the code of conduct
e.g. John Doe [john@doe.com]
2019-02-28 10:10:56
Myriam Heuertz