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Benchmarking software tools for detecting and quantifying selection in evolve and resequencing studies

BACKGROUND: The combination of experimental evolution with whole-genome resequencing of pooled individuals, also called evolve and resequence (E&R) is a powerful approach to study the selection processes and to infer the architecture of adaptive variation. Given the large potential of this metho...

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Detalles Bibliográficos
Autores principales: Vlachos, Christos, Burny, Claire, Pelizzola, Marta, Borges, Rui, Futschik, Andreas, Kofler, Robert, Schlötterer, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694636/
https://www.ncbi.nlm.nih.gov/pubmed/31416462
http://dx.doi.org/10.1186/s13059-019-1770-8
Descripción
Sumario:BACKGROUND: The combination of experimental evolution with whole-genome resequencing of pooled individuals, also called evolve and resequence (E&R) is a powerful approach to study the selection processes and to infer the architecture of adaptive variation. Given the large potential of this method, a range of software tools were developed to identify selected SNPs and to measure their selection coefficients. RESULTS: In this benchmarking study, we compare 15 test statistics implemented in 10 software tools using three different scenarios. We demonstrate that the power of the methods differs among the scenarios, but some consistently outperform others. LRT-1, CLEAR, and the CMH test perform best despite LRT-1 and the CMH test not requiring time series data. CLEAR provides the most accurate estimates of selection coefficients. CONCLUSION: This benchmark study will not only facilitate the analysis of already existing data, but also affect the design of future data collections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1770-8) contains supplementary material, which is available to authorized users.