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Molecular Diagnostic Quality Assurance

Summary

  • Universal sample requirements for molecular diagnostics

  • Strategies to deal with common challenges

  • Challenges unique to PCR assays

  • Challenges unique to DNA fluorescent assays

  • Challenges unique to NGS assays

  • Challenges unique to newer molecular technologies

Overview

Since the beginning of the PCR revolution in the 1980s, molecular diagnostics have proven to be a useful tool for the clinical laboratory.  The ability to analyze a variety of samples for DNA and RNA content have proven to be useful for a large number of clinical conditions using a number of different technologies.  However, each technology has its pitfalls with how to handle samples for optimal results.  In addition, different technologies have different challenges as to what can inhibit optimal results, and each technology has a unique solution to these pitfalls.

Who should attend?

  • Quality control

  • Assay Development

  • Assay validation

  • Research and Development

  • Clinical Diagnostics

Todd Graham

Expert

Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics.

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