Bent Petersen

Dr. Bent Petersen

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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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12 December 2014 in Science
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EJErich D. Jarvis
Erich D. Jarvis
SMSiavash Mirarab
Siavash Mirarab
AAAndre J. Aberer
Andre J. Aberer
BLBo Li
Bo Li
PHPeter Houde
Peter Houde
GZGuojie Zhang
Guojie Zhang
To better determine the history of modern birds, we performed a genome-scale phylogenetic analysis of 48 species representing all orders of Neoaves using phylogenomic methods created to handle genome-scale data. We recovered a highly resolved tree that confirms previously controversial sister or close relationships. We identified the first divergence in Neoaves, two groups we named Passerea and Columbea, representing independent lineages of diverse and convergently evolved land and water bird species. Among Passerea, we infer the common ancestor of core landbirds to have been an apex predator and confirm independent gains of vocal learning. Among Columbea, we identify pigeons and flamingoes as belonging to sister clades. Even with whole genomes, some of the earliest branches in Neoaves proved challenging to resolve, which was best explained by massive protein-coding sequence convergence and high levels of incomplete lineage sorting that occurred during a rapid radiation after the Cretaceous-Paleogene mass extinction event about 66 million years ago.

8 March 2019 in Nature Communications
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RHRene S. Hendriksen
Rene S. Hendriksen
PMPatrick Munk
Patrick Munk
PNPatrick Murigu Kamau Njage
Patrick Murigu Kamau Njage
BBBram Van Bunnik
Bram Van Bunnik
LMLuke McNally
Luke McNally
FAFrank Møller Aarestrup
Frank Møller Aarestrup
Antimicrobial resistance (AMR) is a serious threat to global public health, but obtaining representative data on AMR for healthy human populations is difficult. Here, we use metagenomic analysis of untreated sewage to characterize the bacterial resistome from 79 sites in 60 countries. We find systematic differences in abundance and diversity of AMR genes between Europe/North-America/Oceania and Africa/Asia/South-America. Antimicrobial use data and bacterial taxonomy only explains a minor part of the AMR variation that we observe. We find no evidence for cross-selection between antimicrobial classes, or for effect of air travel between sites. However, AMR gene abundance strongly correlates with socio-economic, health and environmental factors, which we use to predict AMR gene abundances in all countries in the world. Our findings suggest that global AMR gene diversity and abundance vary by region, and that improving sanitation and health could potentially limit the global burden of AMR. We propose metagenomic analysis of sewage as an ethically acceptable and economically feasible approach for continuous global surveillance and prediction of AMR.

26 June 2013 in Nature
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LOLudovic Orlando
Ludovic Orlando
AGAurélien Ginolhac
Aurélien Ginolhac
GZGuojie Zhang
Guojie Zhang
DFDuane Froese
Duane Froese
AAAnders Albrechtsen
Anders Albrechtsen
EWEske Willerslev
Eske Willerslev

20 February 2019 in Proteins: Structure, Function, and Bioinformatics
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MKMichael Schantz Klausen
Michael Schantz Klausen
MJMartin Closter Jespersen
Martin Closter Jespersen
HNHenrik Nielsen
Henrik Nielsen
KJKamilla Kjærgaard Jensen
Kamilla Kjærgaard Jensen
VJVanessa Isabell Jurtz
Vanessa Isabell Jurtz
PMPaolo Marcatili
Paolo Marcatili

31 July 2009 in BMC Structural Biology
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BPBent Petersen
Bent Petersen
TPThomas Nordahl Petersen
Thomas Nordahl Petersen
PAPernille Andersen
Pernille Andersen
MNMorten Nielsen
Morten Nielsen
CLClaus Lundegaard
Claus Lundegaard
Background: Estimation of the reliability of specific real value predictions is nontrivial and the efficacy of this is often questionable. It is important to know if you can trust a given prediction and therefore the best methods associate a prediction with a reliability score or index. For discrete qualitative predictions, the reliability is conventionally estimated as the difference between output scores of selected classes. Such an approach is not feasible for methods that predict a biological feature as a single real value rather than a classification. As a solution to this challenge, we have implemented a method that predicts the relative surface accessibility of an amino acid and simultaneously predicts the reliability for each prediction, in the form of a Z-score. Results: An ensemble of artificial neural networks has been trained on a set of experimentally solved protein structures to predict the relative exposure of the amino acids. The method assigns a reliability score to each surface accessibility prediction as an inherent part of the training process. This is in contrast to the most commonly used procedures where reliabilities are obtained by post-processing the output. Conclusion: The performance of the neural networks was evaluated on a commonly used set of sequences known as the CB513 set. An overall Pearson's correlation coefficient of 0.72 was obtained, which is comparable to the performance of the currently best public available method, Real-SPINE. Both methods associate a reliability score with the individual predictions. However, our implementation of reliability scores in the form of a Z-score is shown to be the more informative measure for discriminating good predictions from bad ones in the entire range from completely buried to fully exposed amino acids. This is evident when comparing the Pearson's correlation coefficient for the upper 20% of predictions sorted according to reliability. For this subset, values of 0.79 and 0.74 are obtained using our and the compared method, respectively. This tendency is true for any selected subset.

11 November 2020 in Nature
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SFShaohong Feng
Shaohong Feng
JSJosefin Stiller
Josefin Stiller
YDYuan Deng
Yuan Deng
JAJoel Armstrong
Joel Armstrong
QFQi Fang
Qi Fang
GZGuojie Zhang
Guojie Zhang
Whole-genome sequencing projects are increasingly populating the tree of life and characterizing biodiversity1,2,3,4. Sparse taxon sampling has previously been proposed to confound phylogenetic inference5, and captures only a fraction of the genomic diversity. Here we report a substantial step towards the dense representation of avian phylogenetic and molecular diversity, by analysing 363 genomes from 92.4% of bird families—including 267 newly sequenced genomes produced for phase II of the Bird 10,000 Genomes (B10K) Project. We use this comparative genome dataset in combination with a pipeline that leverages a reference-free whole-genome alignment to identify orthologous regions in greater numbers than has previously been possible and to recognize genomic novelties in particular bird lineages. The densely sampled alignment provides a single-base-pair map of selection, has more than doubled the fraction of bases that are confidently predicted to be under conservation and reveals extensive patterns of weak selection in predominantly non-coding DNA. Our results demonstrate that increasing the diversity of genomes used in comparative studies can reveal more shared and lineage-specific variation, and improve the investigation of genomic characteristics. We anticipate that this genomic resource will offer new perspectives on evolutionary processes in cross-species comparative analyses and assist in efforts to conserve species.