I have diverse research interests, including genome evolution and function, fungal pathogenicity, phylogenomics, and software engineering for the life sciences. For example, I aim to unravel the evolutionary modes and molecular mechanisms that contribute to fungal pathogenicity. This work has implications for the development of new strategies for identifying, preventing, and combatting fungal infections.

In addition to my research, I am deeply committed to promoting diversity, equity, and inclusion in science. I am involved in efforts that aim to increase the representation of underrepresented groups in STEM fields. I am also passionate about science communication and outreach and regularly participate in community engagement events to share research and foster a dialogue between scientists and the public.

To this end, I write a broadly accessible newsletter titled Genomely: where genomics and evolution converge. Genomely’s blog is to exploring the world of genomics, with a special focus on evolutionary and comparative studies. Subscribe for free!

Research Interests

Genome Evolution and Function

about_images/diversity_of_yeasts.jpg Determining the principles of genome function and evolution is a major goal in evolutionary biology. The Saccharomycotina subphylum of yeasts are a remarkably diverse group of organisms. In fact, budding yeast diversity is roughly on par with the animal and plant kingdoms (see figure from Shen et al. 2018, Cell). As part of the Y1000+ initiative, sequencing and analysis of 1,000+ budding yeast species is underway. To date, numerous insights into the tempo and mode of genome evolution across approximately 400 million years have been made. For example, a genetic network inferred from evolutionary information captured conserved cellular structure and genome function (Steenwyk et al. 2022, Science Advances). Discoveries have also been made among specific lineages; for example, budding yeast from the genus Hanseniaspora have lost numerous cell cycle and DNA repair genes (Steenwyk et al. 2019, PLOS Biology). This discovery is in conflict with current wisdom, which suggests these genes are important to all life and therefore evolutionarily 'resistant' to change. These and other studies highlight conservation and flexibility in dynamics of genome evolution.

Representative publications:
Steenwyk et al. (2022) Science Advances
Steenwyk et al. (2019) PLOS Biology
Steenwyk & Rokas (2016) G3

Fungal Pathogenicity

about_images/hybrids_graphical_abstract.jpg Filamentous fungi including species from the genera Aspergillus and Candida are of medical and technologic importance. Some species pose threats to human or plant health while others produce mainstay pharmaceuticals like penicillin. Studies unraveling the evolutionary history of these genera will help uncover the molecular processes that contribute to some microbes being harmful to humans while others are helpful. In one study, we investigated the evolutionary history of globally distributed clinical isolates of Aspergillus latus, which led to the discovery that A. latus originated from allodiploid hybridization wherein the genome content of both parental species is maintained (see figure from Steenwyk, Lind et al. 2020, Current Biology). Aspergillus hybrids exhibited phenotypic heterogeneity and were distinct from closely related species including their parents and their close relatives. These results suggest that allodiploid hybridization contributes to the evolution of filamentous fungal pathogens. In a separate study, genomic and phenotypic analysis revealed the genomes of nonpathogenic Aspergillus fungi encoded genes known to impact virulence and have similar phenotypic profiles compared to pathogenic species (Steenwyk et al. 2020, Genetics). These findings raise the question of "what makes a pathogen?"

Representative publications:
Steenwyk et al. (2023) PLOS Pathogens
Steenwyk, Lind et al. (2020) Current Biology
Steenwyk et al. (2020) Genetics


about_images/about_images/clipkit_performance.jpg Phylogenomics aims to elucidate the evolutionary history of species, genes, and other biological entities. Several projects aim to determine the evolutionary history among lineages such as fungi (e.g., see figure from Li et al. 2021, Current Biology) and other projects aim to develop novel methods in phylogenomics (e.g., Shen et al. 2021, Systematic Biology). These studies help provide the necessary backbone to study the evolution of traits, genes, and other biological entities. Moreover, divergence time analysis has also placed the evolutionary history of some lineages in geologic time, enabling insights to when certain lineages arose (Steenwyk et al. 2019, mBio) These and other studies have revealed many aspects of evolutionary histories, including the prominence of incongruence — that is, conflicting phylogenetic hypotheses. Together with a rich history of literature, we recently synthesized incongruence, methods to ameliorate it, and identified avenues for future research (Steenwyk et al. 2023, Nature Reviews Genetics), capturing the maturation of the field.

Representative publications:
Steenwyk et al. (2023) Nature Reviews Genetics
Shen et al. (2021) Systematic Biology
Li et al. (2021) Current Biology
Steenwyk et al. (2019) mBio

Development of Computational Tools

about_images/about_images/clipkit_performance.jpg Research in the biological sciences — such as evolutionary biology, molecular biology, and others — often relies on computational tools. To equip bioinformaticians with the necessary computational tools, I have developed multiple software. For example, ClipKIT an alignment trimming algorithm that retains phylogenetically informative sites and removes the rest, outperformed other alignment trimming methods across a total of ~140 thousand alignments (see figure from Steenwyk et al. 2020, PLOS Biology; browser application). PhyKIT, a Swiss-army knife toolkit for processing and analyzing multiple sequence alignments and phylogenies, facilitates determining information content in phylogenomic data matrices, conduct evolution-based screens of gene function, and identify putative signatures of rapid radiation events among other things (Steenwyk et al. 2021, Bioinformatics). A complete list of software I have developed can be found on the software page.

Representative publications:
Steenwyk et al. (2022) PLOS Biology
Steenwyk et al. (2021) Bioinformatics
Steenwyk et al. (2020) PLOS Biology


These research aims have been enabled by collaborative efforts. A non-exhaustive list of collaborator/friend labs include the following: Rokas, Shen, Hittinger, Oberlies, and the Goldman laboratories. I am always interested in collaboration because what we can achieve together is far greater than what we can achieve alone - please feel free to get in touch.

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