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dc.contributor.authorBarata, Carolina De Castro Barbosa Rodrigues
dc.contributor.authorBorges, Rui
dc.contributor.authorKosiol, Carolin
dc.date.accessioned2022-12-22T10:30:06Z
dc.date.available2022-12-22T10:30:06Z
dc.date.issued2023-01-09
dc.identifier272668076
dc.identifierc97214e0-776b-4dfa-a56e-e65cb29dfb50
dc.identifier85144905694
dc.identifier36544394
dc.identifier000901580800001
dc.identifier.citationBarata , C D C B R , Borges , R & Kosiol , C 2023 , ' Bait-ER : a Bayesian method to detect targets of selection in Evolve-and-Resequence experiments ' , Journal of Evolutionary Biology , vol. 36 , no. 1 , pp. 29-44 . https://doi.org/10.1111/jeb.14134en
dc.identifier.issn1010-061X
dc.identifier.otherORCID: /0000-0002-4086-1636/work/125303076
dc.identifier.urihttps://hdl.handle.net/10023/26644
dc.descriptionfunding: This research was funded in part, by the Vienna Science and Technology Fund (WWTF) [MA16-061], the Biotechnology and Biological Sciences Research Council (BBSRC) [BB/W000768/1], and the Austrian Science Fund (FWF) [P34524-B]. CK received funding from the Royal Society (RG170315) and Carnegie Trust (RIG007474). The computational results presented have been partly achieved using the St Andrews Bioinformatics Unit (StABU), which is funded by a Wellcome Trust ISSF award (grant 105621/Z/14/Z).en
dc.description.abstractFor over a decade, experimental evolution has been combined with high-throughput sequencing techniques. In so-called Evolve-and-Resequence (E&R) experiments, populations are kept in the laboratory under controlled experimental conditions where their genomes are sampled and allele frequencies monitored. However, identifying signatures of adaptation in E&R datasets is far from trivial, and it is still necessary to develop more efficient and statistically sound methods for detecting selection in genome-wide data. Here, we present Bait-ER – a fully Bayesian approach based on the Moran model of allele evolution to estimate selection coefficients from E&R experiments. The model has overlapping generations, a feature that describes several experimental designs found in the literature. We tested our method under several different demographic and experimental conditions to assess its accuracy and precision, and it performs well in most scenarios. Nevertheless, some care must be taken when analysing trajectories where drift largely dominates and starting frequencies are low. We compare our method with other available software and report that ours has generally high accuracy even for trajectories whose complexity goes beyond a classical sweep model. Furthermore, our approach avoids the computational burden of simulating an empirical null distribution, outperforming available software in terms of computational time and facilitating its use on genome-wide data. We implemented and released our method in a new open-source software package that can be accessed at https://doi.org/10.5281/zenodo.7351736.
dc.format.extent16
dc.format.extent2927553
dc.language.isoeng
dc.relation.ispartofJournal of Evolutionary Biologyen
dc.subjectBayesian inferenceen
dc.subjectSelection coefficientsen
dc.subjectTargets of selectionen
dc.subjectE&Ren
dc.subjectMoran modelen
dc.subjectPool-seqen
dc.subjectQA75 Electronic computers. Computer scienceen
dc.subjectQH301 Biologyen
dc.subjectQH426 Geneticsen
dc.subject3rd-DASen
dc.subjectMCCen
dc.subject.lccQA75en
dc.subject.lccQH301en
dc.subject.lccQH426en
dc.titleBait-ER : a Bayesian method to detect targets of selection in Evolve-and-Resequence experimentsen
dc.typeJournal articleen
dc.contributor.sponsorBBSRCen
dc.contributor.sponsorVienna Science and Technology Funden
dc.contributor.sponsorThe Royal Societyen
dc.contributor.sponsorCarnegie Trusten
dc.contributor.sponsorThe Wellcome Trusten
dc.contributor.sponsorAustrian Science Fund FWFen
dc.contributor.institutionUniversity of St Andrews. Centre for Biological Diversityen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.identifier.doi10.1111/jeb.14134
dc.description.statusPeer revieweden
dc.identifier.urlhttps://doi.org/10.1101/2020.12.15.422880en
dc.identifier.grantnumberBB/W000768/1en
dc.identifier.grantnumberMA16-061en
dc.identifier.grantnumberRG170315en
dc.identifier.grantnumberRIG007474en
dc.identifier.grantnumber105621/Z/14/Zen
dc.identifier.grantnumberN/Aen


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