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Emily A. Vetter

Researcher at Mayo Clinic

Publications -  34
Citations -  2988

Emily A. Vetter is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Becton dickinson & Chocolate agar. The author has an hindex of 25, co-authored 34 publications receiving 2796 citations.

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Real-Time PCR in Clinical Microbiology: Applications for Routine Laboratory Testing

TL;DR: Real-time PCR assays provide sensitivity and specificity equivalent to that of conventional PCR combined with Southern blot analysis, and since amplification and detection steps are performed in the same closed vessel, the risk of releasing amplified nucleic acids into the environment is negligible.
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Culture with BACTEC Peds Plus/F Bottle Compared with Conventional Methods for Detection of Bacteria in Synovial Fluid

TL;DR: Results indicate the superior performance of the BACTEC Peds Plus/F bottle over the conventional agar plate method for the detection of clinically significant microorganisms from synovial fluid specimens.
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Analysis of 281,797 Consecutive Blood Cultures Performed over an Eight-Year Period: Trends in Microorganisms Isolated and the Value of Anaerobic Culture of Blood

TL;DR: The value of the NVTSB anaerobic blood culture was demonstrated for diagnosing bloodstream infections caused by certain facultatively anaerilic bacteria in addition to obligately anaerobia bacteria and supported the inclusion of theNVTSB a standard part of the three-component blood culture set used at this institution.
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Comparison of LightCycler PCR, Rapid Antigen Immunoassay, and Culture for Detection of Group A Streptococci from Throat Swabs

TL;DR: The LightCycler PCR is a suitable stand-alone method for the detection of GAS from throat swabs and requires less than half the personnel time and the procedure can be completed in considerably less time than the standard approach.
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Three-Hour Molecular Detection of Campylobacter, Salmonella, Yersinia, and Shigella Species in Feces with Accuracy as High as That of Culture

TL;DR: A panel of rapid PCR assays for the detection and identification of C. jejuni, C. coli, Salmonella, and Yersinia species and Shigella and enteroinvasive E. coli in stool samples has a sensitivity and specificity equivalent to that of culture for stools in Cary Blair transport medium.