Guy Baele

Dr. Guy Baele

Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, 3000 Leuven, Belgium
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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 April 2018 in Systematic Biology
Verified
Journal Article
Open access
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ARAndrew Rambaut
Andrew Rambaut
ADAlexei J Drummond
Alexei J Drummond
DXDong Xie
Dong Xie
GBGuy Baele
Guy Baele
MSMarc A Suchard
Marc A Suchard
Bayesian inference of phylogeny using Markov chain Monte Carlo (MCMC) plays a central role in understanding evolutionary history from molecular sequence data. Visualizing and analyzing the MCMC-generated samples from the posterior distribution is a key step in any non-trivial Bayesian inference. We present the software package Tracer (version 1.7) for visualizing and analyzing the MCMC trace files generated through Bayesian phylogenetic inference. Tracer provides kernel density estimation, multivariate visualization, demographic trajectory reconstruction, conditional posterior distribution summary, and more. Tracer is open-source and available at http://beast.community/tracer.

1 January 2018 in Virus Evolution
Verified
Journal Article
Open access
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MSMarc A Suchard
Marc A Suchard
PLPhilippe Lemey
Philippe Lemey
GBGuy Baele
Guy Baele
DADaniel L Ayres
Daniel L Ayres
ADAlexei J Drummond
Alexei J Drummond
ARAndrew Rambaut
Andrew Rambaut
The Bayesian Evolutionary Analysis by Sampling Trees (BEAST) software package has become a primary tool for Bayesian phylogenetic and phylodynamic inference from genetic sequence data. BEAST unifies molecular phylogenetic reconstruction with complex discrete and continuous trait evolution, divergence-time dating, and coalescent demographic models in an efficient statistical inference engine using Markov chain Monte Carlo integration. A convenient, cross-platform, graphical user interface allows the flexible construction of complex evolutionary analyses.

7 March 2012 in Molecular Biology and Evolution
Verified
Journal Article
Closed access
GBGuy Baele
Guy Baele
PLPhilippe Lemey
Philippe Lemey
TBTrevor Bedford
Trevor Bedford
ARAndrew Rambaut
Andrew Rambaut
MSMarc A. Suchard
Marc A. Suchard
AAAlexander Alekseyenko
Alexander Alekseyenko
Recent developments in marginal likelihood estimation for model selection in the field of Bayesian phylogenetics and molecular evolution have emphasized the poor performance of the harmonic mean estimator (HME). Although these studies have shown the merits of new approaches applied to standard normally distributed examples and small real-world data sets, not much is currently known concerning the performance and computational issues of these methods when fitting complex evolutionary and population genetic models to empirical real-world data sets. Further, these approaches have not yet seen widespread application in the field due to the lack of implementations of these computationally demanding techniques in commonly used phylogenetic packages. We here investigate the performance of some of these new marginal likelihood estimators, specifically, path sampling (PS) and stepping-stone (SS) sampling for comparing models of demographic change and relaxed molecular clocks, using synthetic data and real-world examples for which unexpected inferences were made using the HME. Given the drastically increased computational demands of PS and SS sampling, we also investigate a posterior simulation-based analogue of Akaike's information criterion (AIC) through Markov chain Monte Carlo (MCMC), a model comparison approach that shares with the HME the appealing feature of having a low computational overhead over the original MCMC analysis. We confirm that the HME systematically overestimates the marginal likelihood and fails to yield reliable model classification and show that the AICM performs better and may be a useful initial evaluation of model choice but that it is also, to a lesser degree, unreliable. We show that PS and SS sampling substantially outperform these estimators and adjust the conclusions made concerning previous analyses for the three real-world data sets that we reanalyzed. The methods used in this article are now available in BEAST, a powerful user-friendly software package to perform Bayesian evolutionary analyses.

23 November 2011 in Nature
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Journal Article
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MGMiodrag Grbic
Miodrag Grbic
TLThomas Van Leeuwen
Thomas Van Leeuwen
RCRichard M. Clark
Richard M. Clark
SRStephane Rombauts
Stephane Rombauts
PRPierre Rouzé
Pierre Rouzé
YPYves Van de Peer
Yves Van de Peer
The spider mite Tetranychus urticae is a cosmopolitan agricultural pest with an extensive host plant range and an extreme record of pesticide resistance. Here we present the completely sequenced and annotated spider mite genome, representing the first complete chelicerate genome. At 90 megabases T. urticae has the smallest sequenced arthropod genome. Compared with other arthropods, the spider mite genome shows unique changes in the hormonal environment and organization of the Hox complex, and also reveals evolutionary innovation of silk production. We find strong signatures of polyphagy and detoxification in gene families associated with feeding on different hosts and in new gene families acquired by lateral gene transfer. Deep transcriptome analysis of mites feeding on different plants shows how this pest responds to a changing host environment. The T. urticae genome thus offers new insights into arthropod evolution and plant–herbivore interactions, and provides unique opportunities for developing novel plant protection strategies.

3 October 2014 in Science
Verified
Journal Article
Closed access
PDF file
NFNuno Rodrigues Faria
Nuno Rodrigues Faria
ARAndrew Rambaut
Andrew Rambaut
MSMarc A. Suchard
Marc A. Suchard
GBGuy Baele
Guy Baele
TBTrevor Bedford
Trevor Bedford
PLPhilippe Lemey
Philippe Lemey
The hidden history of the HIV pandemic: Rail and river transport in 1960s Congo, combined with the sexual revolution and changes in health care practices, primed the HIV pandemic. Fariaet al.unpick the circumstances surrounding the ascendancy of HIV from its origins before 1920 in chimpanzee hunters in the Cameroon to amplification in Kinshasa. Around 1960, rail links promoted the spread of the virus to mining areas in southeastern Congo and beyond. Ultimately, HIV crossed the Atlantic in Haitian teachers returning home. From those early events, a pandemic was born.Science, this issue p.56

1 September 2016 in Cell
Verified
Journal Article
Open access
BGBrigida Gallone
Brigida Gallone
JSJan Steensels
Jan Steensels
TPTroels Prahl
Troels Prahl
LSLeah Soriaga
Leah Soriaga
VSVeerle Saels
Veerle Saels
KVKevin Verstrepen
Kevin Verstrepen
Whereas domestication of livestock, pets, and crops is well documented, it is still unclear to what extent microbes associated with the production of food have also undergone human selection and where the plethora of industrial strains originates from. Here, we present the genomes and phenomes of 157 industrial Saccharomyces cerevisiae yeasts. Our analyses reveal that today's industrial yeasts can be divided into five sublineages that are genetically and phenotypically separated from wild strains and originate from only a few ancestors through complex patterns of domestication and local divergence. Large-scale phenotyping and genome analysis further show strong industry-specific selection for stress tolerance, sugar utilization, and flavor production, while the sexual cycle and other phenotypes related to survival in nature show decay, particularly in beer yeasts. Together, these results shed light on the origins, evolutionary history, and phenotypic diversity of industrial yeasts and provide a resource for further selection of superior strains. PAPERCLIP.