Publications by authors named "B Strope"

Article Synopsis
  • Xenograft models simulate human tumor biology, allowing researchers to manipulate the tumor microenvironment and examine drug responses.
  • Spatially resolved transcriptomics (SRT) is a technique that helps analyze the spatial organization of these models but lacks specialized processing pipelines.
  • Xenomake is a new standalone pipeline designed to automate the handling of spatial xenograft reads, improving data processing, alignment, and analysis while ensuring biological relevance.
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The increased feasibility of whole-genome sequencing has generated significant interest in using such molecular diagnostic approaches to characterize difficult-to-treat, antimicrobial-resistant (AMR) infections. Nevertheless, there are current limitations in the accurate prediction of AMR phenotypes based on existing AMR gene database approaches, which primarily correlate a phenotype with the presence/absence of a single AMR gene. Our study utilized a large cohort of cephalosporin-susceptible bacteremia samples to determine how increasing the dosage of narrow-spectrum β-lactamase-encoding genes in conjunction with other diverse β-lactam/β-lactamase inhibitor (BL/BLI) genetic determinants contributes to progressively more severe BL/BLI phenotypes.

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Xenograft models are attractive models that mimic human tumor biology and permit one to perturb the tumor microenvironment and study its drug response. Spatially resolved transcriptomics (SRT) provide a powerful way to study the organization of xenograft models, but currently there is a lack of specialized pipeline for processing xenograft reads originated from SRT experiments. Xenomake is a standalone pipeline for the automated handling of spatial xenograft reads.

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Extended-spectrum cephalosporin-resistant (ESC-R-) is an urgent public health threat with sequence type clonal complex 131 (STc131), phylogroup B2 strains being particularly concerning as the dominant cause of ESC-R- infections. To address the paucity of recent ESC-R- molecular epidemiology data in the United States, we used whole-genome sequencing (WGS) to fully characterize a large cohort of invasive ESC-R- at a tertiary care cancer center in Houston, Texas, collected from 2016 to 2020. During the study time frame, there were 1,154 index bloodstream infections (BSIs) of which 389 (33.

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Unlabelled: Extended-spectrum cephalosporin resistant (ESC-R- ) is an urgent public health threat with sequence type clonal complex 131 (STc131), phylogroup B2 strains being particularly concerning as the dominant cause of ESC-R- infections. To address the paucity of recent ESC-R- molecular epidemiology data in the United States, we used whole genome sequencing (WGS) to fully characterize a large cohort of invasive ESC-R- at a tertiary care cancer center in Houston, Texas collected from 2016-2020. During the study timeframe, there were 1154 index bloodstream infections (BSIs) of which 389 (33.

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