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Right here, we describe refinements that expand the number of patient samples which can be prepared at one time, increasing the utility with this technology for quickly responding to growing infectious diseases. We utilized dengue virus (DENV) as a model system since much has already been understood about the antibody response. Sera from main DENV-infected patients (n = 28) were used to pan an MS2 bacteriophage VLP library showing all feasible 10-amino-acid peptides from the DENV polypeptide. Selected VLPs ha
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