Join us for the webinar

Validation of Error-Corrected Sequencing for Hematological Malignancies

presented by Drs. Sarah Rapisardo and Catherine Rehder

at Duke University

 October 11, 2018 at 11:00pm Hong Kong Time / October 11, 2018 at 11:00am EDT

Drs. Rapisardo and Rehder will discuss a validation study for the Archer® VariantPlex® Myeloid assay for hematological malignancies. They will also discuss their work to expand testing with a custom Archer FusionPlex® assay to detect known and novel fusions, with a focus on Ph-like ALL fusions.

This webinar broadcast is sponsored by ArcherDX and hosted by GenomeWeb.

Date and time: Thursday, October 11, 2018 11:00 pm 
China Time (Hong Kong/Beijing, GMT+08:00) 
  Thursday, October 11, 2018 8:00 am 
Pacific Daylight Time (San Francisco, GMT-07:00)
  Thursday, October 11, 2018 5:00 pm
Europe Summer Time (Paris, GMT+02:00)
Duration: 1 hour
Description:

This webinar will discuss a validation study for a next-generation sequencing (NGS) assay for hematological malignancies (e.g., acute myeloid leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, and myeloproliferative neoplasms).

Diagnostic and prognostic testing methodologies in hematological malignancies are evolving beyond traditional chromosome analysis, fluorescent in situ hybridization, and single-analyte molecular testing toward NGS because it enables the detection of multiple molecular driver mutations and oncogenic fusions in a single assay. However, most NGS approaches are limited in their ability to detect fusions, or to detect known pathogenic variants in specific genes such as CEBPA and FLT3 without using additional molecular methodologies. The ability to quickly and accurately identify specific translocation partners and the presence of specific pathogenic variants is critical in the era of increasingly personalized treatment plans.

In this webinar, Drs. Catherine Rehder and Sarah Rapisardo at Duke University will describe their efforts to validate the Archer VariantPlex Myeloid assay. They will also discuss their work to expand testing with a custom Archer FusionPlex assay to detect known and novel fusions, with a focus on Ph-like ALL fusions.

Drs. Rehder and Rapisardo will detail their initial proof-of-principle studies, which have demonstrated 100 percent concordance with their current assays, with superior coverage of previously problematic regions and significant improvements in library complexity.

Speakers:
Sarah Rapisardo, PhD, DABMGG
Assistant Director, Clinical Cytogenetics and Molecular Diagnostics Laboratories
Duke University Health System

Dr. Sarah Rapisardo graduated with a PhD in Molecular Cancer Biology from Duke University. After completing ABMGG postdoctoral fellowships in Clinical Cytogenetics and Clinical Molecular Genetics at Duke, she started as an Assistant Professor in the Department of Pathology at Duke. In her current position as Assistant Director of the Clinical Cytogenetics and Molecular Diagnostics Laboratories, she is involved in a broad range of clinical cytogenetic and molecular testing and assay development, including postnatal germline analysis and the evaluation of acquired neoplastic abnormalities.

Dr. Rapisardo is especially interested in implementing next-generation sequencing for testing in hematological malignancies and has led the validation work for the myeloid NGS panel.

Catherine Rehder, PhD, FACMG
Director, Duke Cytogenetics Laboratory
Associate Director, Duke Molecular Diagnostics Laboratory
Duke University Health System

Dr. Catherine Rehder graduated with a PhD in human genetics from Virginia Commonwealth University. After completing American Board of Medical Genetics and Genomics (ABMGG) Clinical Cytogenetics and Clinical Molecular Genetics fellowships at Duke University in 2007, she became an Assistant Professor of Pathology at Duke. Dr. Rehder spent six years as a member of the ACMG Laboratory Quality Assurance Committee, serving as Chair for two years. She was also elected to the ACMG Board of Directors in 2017.

Dr. Rehder is active in the genetics community in North Carolina, serving as a co-investigator on NICHD-funded newborn screening pilot studies for mucopolysaccharidosis I and X-linked adrenoleukodystrophy. She is also an advisor to the Early Check voluntary newborn screening program. Her primary areas of interest include reporting practices of genomic testing, Pompe disease and other glycogen storage diseases, as well as newborn screening and cancer cytogenetics.

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