AUG 20, 2014 08:30 AM PDT
Actionable mutation detection with multiplex pcr-based targeted enrichment approach for next generation sequencing (NGS)
Presented at the Genetics and Genomics Virtual Event
CONTINUING EDUCATION (CME/CE/CEU) CREDITS: CE | CEU
16 48 2047

Speakers:
  • Director, Head of Biological research content, Qiagen, Inc.
    Biography
      Dr. Devgan is the head of the Biological Research Content, QIAGEN. He received his Ph.D. in molecular biology and conducted post-doctoral research at Harvard Medical School before moving to the biotechnology industry. He received his MBA from the University of Wurzburg in Germany and has spent many years as a scientist in developing new technologies and products clinical and translational research.

    Abstract:
    Next-generation sequencing (NGS) has revolutionized extraction of genomic information, facilitating rapid advances in the fields of clinical research and molecular diagnostics. However, certain bottlenecks still pose challenges in implementing NGS for clinical research. To meet these challenges, QIAGEN introduced 14 panels for targeted enrichment of up to 570 clinically-relevant genes, the largest portfolio of panels for assessing cancer genes in a clinical research setting. GeneRead DNAseq Gene Panel V2 integrates with bioinformatics solutions, allowing customization of assays and streamlined data analysis and interpretation for fast generation of valuable insights. This webinar will discuss the utilization of these panels highlighting their analytical performance and applicability in a clinical research setting.

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