Evidence map›Paper›PMID 36544394›Full record

ArticleJournal of evolutionary biology2023

Bait-ER: A Bayesian method to detect targets of selection in Evolve-and-Resequence experiments.

Carolina Barata, Rui Borges, Carolin Kosiol

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Article in Journal of evolutionary biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Carolina BarataCentre for Biological Diversity, University of St Andrews, St Andrews, UK.ORCID 0000-0003-1945-2245
Rui BorgesInstitute of Population Genetics, Wien, Austria.ORCID 0000-0002-5905-3778
Carolin KosiolCentre for Biological Diversity, University of St Andrews, St Andrews, UK.ORCID 0000-0002-3219-6648

Funding

Biotechnology and Biological Sciences Research Council BB/W000768/1Wellcome Trust 105621/Z/14/Z
6 · The paper itself

Abstract

For 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.

Indexed as

Selection, GeneticSoftwareAdaptation, PhysiologicalBayes TheoremGene FrequencyBayesian inferenceE&RMoran modelpool-seqselection coefficientstargets of selection

Identifiers

PMID36544394
PMCPMC10108205

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.