Norman J. Wickett

Norman J. Wickett

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Norman J. Wickett

Department of Botany and Biodiversity Research University of Vienna Vienna Austria

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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10 April 2011 in Nature
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Journal Article
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YJYuannian Jiao
Yuannian Jiao
NWNorman J. Wickett
Norman J. Wickett
SASaravanaraj Ayyampalayam
Saravanaraj Ayyampalayam
ACAndré S. Chanderbali
André S. Chanderbali
LLLena Landherr
Lena Landherr
CDClaude W. Depamphilis
Claude W. Depamphilis

29 October 2014 in Proceedings of the National Academy of Sciences
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Journal Article
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NWNorman J. Wickett
Norman J. Wickett
SMSiavash Mirarab
Siavash Mirarab
NNNam Nguyen
Nam Nguyen
TWTandy Warnow
Tandy Warnow
ECEric Carpenter
Eric Carpenter
JLJames Leebens-Mack
James Leebens-Mack
Significance: Early branching events in the diversification of land plants and closely related algal lineages remain fundamental and unresolved questions in plant evolutionary biology. Accurate reconstructions of these relationships are critical for testing hypotheses of character evolution: for example, the origins of the embryo, vascular tissue, seeds, and flowers. We investigated relationships among streptophyte algae and land plants using the largest set of nuclear genes that has been applied to this problem to date. Hypothesized relationships were rigorously tested through a series of analyses to assess systematic errors in phylogenetic inference caused by sampling artifacts and model misspecification. Results support some generally accepted phylogenetic hypotheses, while rejecting others. This work provides a new framework for studies of land plant evolution.

12 July 2016 in Applications in Plant Sciences
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MJMatthew G. Johnson
Matthew G. Johnson
EGElliot M. Gardner
Elliot M. Gardner
Yang LiuYang Liu
Yang Liu
RMRafael Medina
Rafael Medina
BGBernard Goffinet
Bernard Goffinet
NWNorman J. Wickett
Norman J. Wickett
Premise of the study: Using sequence data generated via target enrichment for phylogenetics requires reassembly of high‐throughput sequence reads into loci, presenting a number of bioinformatics challenges. We developed HybPiper as a user‐friendly platform for assembly of gene regions, extraction of exon and intron sequences, and identification of paralogous gene copies. We test HybPiper using baits designed to target 333 phylogenetic markers and 125 genes of functional significance in Artocarpus (Moraceae).Methods and Results: HybPiper implements parallel execution of sequence assembly in three phases: read mapping, contig assembly, and target sequence extraction. The pipeline was able to recover nearly complete gene sequences for all genes in 22 species of Artocarpus. HybPiper also recovered more than 500 bp of nontargeted intron sequence in over half of the phylogenetic markers and identified paralogous gene copies in Artocarpus.Conclusions: HybPiper was designed for Linux and Mac OS X and is freely available at https://github.com/mossmatters/HybPiper.

27 October 2014 in GigaScience
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NMNaim Matasci
Naim Matasci
LHLing-Hong Hung
Ling-Hong Hung
ZYZhixiang Yan
Zhixiang Yan
ECEric J Carpenter
Eric J Carpenter
NWNorman J Wickett
Norman J Wickett
GWGane Ka-Shu Wong
Gane Ka-Shu Wong
The 1,000 plants (1KP) project is an international multi-disciplinary consortium that has generated transcriptome data from over 1,000 plant species,

26 January 2012 in Genome Biology
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Journal Article
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YJYuannian Jiao
Yuannian Jiao
JLJames Leebens-Mack
James Leebens-Mack
SASaravanaraj Ayyampalayam
Saravanaraj Ayyampalayam
JBJohn Bowers
John Bowers
MMMichael R McKain
Michael R McKain
CDClaude W Depamphilis
Claude W Depamphilis
Background: Although it is agreed that a major polyploidy event, gamma, occurred within the eudicots, the phylogenetic placement of the event remains unclear. Results: To determine when this polyploidization occurred relative to speciation events in angiosperm history, we employed a phylogenomic approach to investigate the timing of gene set duplications located on syntenic gamma blocks. We populated 769 putative gene families with large sets of homologs obtained from public transcriptomes of basal angiosperms, magnoliids, asterids, and more than 91.8 gigabases of new next-generation transcriptome sequences of non-grass monocots and basal eudicots. The overwhelming majority (95%) of well-resolved gamma duplications was placed before the separation of rosids and asterids and after the split of monocots and eudicots, providing strong evidence that the gamma polyploidy event occurred early in eudicot evolution. Further, the majority of gene duplications was placed after the divergence of the Ranunculales and core eudicots, indicating that the gamma appears to be restricted to core eudicots. Molecular dating estimates indicate that the duplication events were intensely concentrated around 117 million years ago. Conclusions: The rapid radiation of core eudicot lineages that gave rise to nearly 75% of angiosperm species appears to have occurred coincidentally or shortly following the gamma triplication event. Reconciliation of gene trees with a species phylogeny can elucidate the timing of major events in genome evolution, even when genome sequences are only available for a subset of species represented in the gene trees. Comprehensive transcriptome datasets are valuable complements to genome sequences for high-resolution phylogenomic analysis.

24 April 2024 in Nature
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Journal Article
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AZAlexandre R. Zuntini
Alexandre R. Zuntini
TCTom Carruthers
Tom Carruthers
OMOlivier Maurin
Olivier Maurin
PBPaul C. Bailey
Paul C. Bailey
KLKevin Leempoel
Kevin Leempoel
WBWilliam J. Baker
William J. Baker
Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins5–7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes8. This 15-fold increase in genus-level sampling relative to comparable nuclear studies9 provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.