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Charles Boone

Researcher at University of Toronto

Publications -  314
Citations -  46014

Charles Boone is an academic researcher from University of Toronto. The author has contributed to research in topics: Gene & Synthetic genetic array. The author has an hindex of 100, co-authored 294 publications receiving 42217 citations. Previous affiliations of Charles Boone include Canadian Institute for Advanced Research & Queen's University.

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Global Genetic Networks and the Genotype-to-Phenotype Relationship

TL;DR: It is emphasized how information gained from work in yeast translates to other systems, and how a global genetic network not only annotates gene function but also provides new insights into the genotype-to-phenotype relationship.
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Exploring genetic suppression interactions on a global scale

TL;DR: A large-scale study in yeast reveals how defects associated with a mutation in one gene can be compensated for by a second mutation in a suppressor gene, and assembled a global network of genetic suppression interactions, which highlights the major potential for systematic studies of suppression to map cellular function.
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Mode of selection and experimental evolution of antifungal drug resistance in Saccharomyces cerevisiae.

TL;DR: It is shown that mode of selection, degree of dominance of mutations, and ploidy are determining factors in the evolution of resistance to the antifungal drug fluconazole in yeast.
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Systematic yeast synthetic lethal and synthetic dosage lethal screens identify genes required for chromosome segregation

TL;DR: This study shows that systematic genetic screens are a powerful means to discover roles for uncharacterized genes and genes with alternative functions in chromosome maintenance that may not be discovered by using proteomics approaches.
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Bringing order to protein disorder through comparative genomics and genetic interactions

TL;DR: The clear and distinct functional association of flexible and constrained disorder will allow for new approaches and more specific algorithms for disorder detection in a functional context and demonstrate clear evolutionary selection of protein disorder with little selection on primary structure.