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Lillian K. Padgitt-Cobb

Researcher at Oregon State University

Publications -  9
Citations -  71

Lillian K. Padgitt-Cobb is an academic researcher from Oregon State University. The author has contributed to research in topics: Humulus lupulus & Hop (networking). The author has an hindex of 4, co-authored 8 publications receiving 35 citations.

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A draft phased assembly of the diploid Cascade hop (Humulus lupulus) genome.

TL;DR: In this paper, a draft haplotype-phased assembly of the Cascade cultivar genome is presented, which is the most extensive representation of the hop genome to date and provides insight into selective pressures that have driven evolution in hop.
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A phased, diploid assembly of the Cascade hop (Humulus lupulus) genome reveals patterns of selection and haplotype variation

TL;DR: The approaches developed to analyze a phased, diploid assembly of a large plant genome serve to deepen the understanding of the genomic landscape of hop and may have broader applicability to the study of other large, complex genomes.
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Involving community in genes and pathway curation

TL;DR: In two pathway curations jamborees, Plant Reactome curators tested strategies for introducing researchers to pathway curation tools, harnessing biologists’ expertise in curating plant pathways and developing a network of community biocurators.
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Gene expression for secondary metabolite biosynthesis in hop (Humulus lupulus L.) leaf lupulin glands exposed to heat and low-water stress

TL;DR: In this paper, physiological traits and differential gene expression in leaf, stem, and root tissue from hop (Humulus lupulus) cv. USDA Cascade in plants exposed to high temperature stress, low water stress, and a compound treatment of both high temperature and low-water stress for six weeks.
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Genomic analysis of powdery mildew resistance in a hop ( Humulus lupulus L.) bi-parental population segregating for “R6-locus”

TL;DR: Genetic response in hop to fungal pathogen infection has been evaluated at the chromosomal level through QTL analyses but very little information exists on the expression of genes during infection periods, which will prove valuable information for development of precise markers located either within or next to genes responsible for race v4/v6 PM resistance.