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Jeffrey M. Weiss

Researcher at University of Washington

Publications -  13
Citations -  869

Jeffrey M. Weiss is an academic researcher from University of Washington. The author has contributed to research in topics: Gene & Simian immunodeficiency virus. The author has an hindex of 9, co-authored 13 publications receiving 729 citations.

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Pathogenic Influenza Viruses and Coronaviruses Utilize Similar and Contrasting Approaches To Control Interferon-Stimulated Gene Responses

TL;DR: Compared models of the human airway, transcriptomics and proteomics datasets were used to compare ISG response patterns following highly pathogenic H5N1 avian influenza (HPAI) A virus, 2009 pandemic H1N1, severe acute respiratory syndrome coronavirus, and Middle East respiratory syndrome CoV infection, revealing similarities and differences in strategies to control the interferon and innate immune response.
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Tissue-specific transcriptome sequencing analysis expands the non-human primate reference transcriptome resource (NHPRTR)

TL;DR: A major expansion of NHPRTR is described by adding 10.1 billion fragments of tissue-specific RNA-seq data, such that 88% of the reads align to human reference sequences, allowing the full list of expression abundance across all tissues for each species to be computed.
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The non-human primate reference transcriptome resource (NHPRTR) for comparative functional genomics

TL;DR: A large-scale RNA-Seq data and analysis infrastructure is described, the NHP reference transcriptome resource, which presently hosts data from 12 species of primates and is to be expanded to 15 species/subspecies spanning great apes, old world monkeys, new world monkeys and prosimians.
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Next-Generation Sequencing Reveals HIV-1-Mediated Suppression of T Cell Activation and RNA Processing and Regulation of Noncoding RNA Expression in a CD4+ T Cell Line

TL;DR: The first application to the authors' knowledge of next-generation sequencing to the analysis of RNA from a CD4+ T cell line infected with intact HIV is reported, providing insights into alternative viral RNA splice events and the expression of noncoding RNAs, including microRNA host genes.