Webinars and Sponsored Roundtables — Register Now

Wednesday, September 23, 2026. 12 PM-1 PM ET
Roundtable presenters Dr. David Sacks MB, ChB, FRCPath, Chairman, Steering Committee National Glycohemoglobin Standardization Program (NGSP), and Priya Sivaraman, PhD, Senior Technical Product Manager, Tosoh Bioscience.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Thursday, September 24, 2026 11 AM-12 PM CT
This session explores the evolving role of RAS in precision oncology, from the biology of RAS mutations to the expanding landscape of targeted therapies. Through expert presentations, real-world case discussions, and interactive audience polling, participants will examine best practices for RAS biomarker testing across solid tumors, including lung, colorectal, and pancreatic cancers. The session will highlight practical considerations for tissue and liquid biopsy, strategies to address testing gaps, and the importance of multidisciplinary collaboration to ensure timely identification of patients who may benefit from RAS-targeted therapies.

Webinar presenters David Braxton, MD, Chief of Molecular Pathology Services, Hoag Family Cancer Institute & Hoag Memorial Hospital Presbyterian, and Carlos Becerra, MD, Research Director for Medical Oncology, Margaret Given Larkin Endowed Chair for Developmental Cancer Therapeutics, Hoag Memorial Hospital Presbyterian.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Wednesday, September 30, 2026. 1 PM-1:30 PM ET
Roundtable presenters John Longshore, PhD, Head of Scientific Affairs, Global Oncology Diagnostics, AstraZeneca, and Flora Berisha, MS, Executive Director, Global Head of Diagnostic Partnering and Development, Johnson & Johnson Innovative Medicine, and Mark D. Ewalt, MD, Associate Medical Director for Laboratory Operations, Diagnostic Molecular Pathology, Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, and Isabel Preeshagul, DO, MBS, Thoracic Medical Oncologist, Memorial Sloan Kettering Cancer Center.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Tuesday, October 20, 2026 11 AM-12 PM ET
Hear experts review the biological and clinical significance of the HER2 expression continuum in breast tissue, providing a clearer understanding of how these variations might impact diagnosis, and discuss the emerging importance of documenting HER2-low and HER2-ultralow categories using a validated IHC assay.

Webinar presenters Keith Wharton, MD, PhD, Global Medical Affairs Leader–Pathology,
Roche Diagnostics Solutions, and Hannah Y. Wen, MD, PhD, Director, Breast Pathology Fellowship, Associate Team Leader, Breast Pathology Team, Attending Pathologist, Memorial Sloan Kettering Cancer Center.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Next-Generation Sequencing Systems Product Guide, 2023



 

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The outlook for in-house next-generation sequencing

Bringing next-generation sequencing in-house was at the center of a March 27 roundtable led by CAP TODAY publisher Bob McGonnagle, with costs, reimbursement, equity, and the electronic health record part of the conversation. Jeremy Segal, MD, PhD, of the University of Chicago, explains why the Genomics Organization for Academic Laboratories was formed. “By lowering barriers and encouraging cooperation,” he said, “we’ve seen our labs increase the pace of development and the quality of the assays they’re bringing on.”

There’s increasing interest in bringing next-generation sequencing in-house as opposed to sending it to a reference laboratory. While there are costs associated with bringing it in-house, if you look at total cost of the test and turnaround time, it’s an even horse race or slightly preferable to bring it in-house. Luca Quagliata, would you agree with that?

Luca Quagliata, BCMAS, PhD, VP and global head of medical affairs, Thermo Fisher Scientific: I do agree. Cost is an important component of being able to bring these tests in-house. We often think cost is driven only by reagents, but it’s not the component that most impacts overall expenditure. Cost of personnel to perform the analysis is equally important. With solutions that are going toward fully automated or semiautomated systems, you can free hands, better utilize the lab workforce, and effectively maximize budget.

The other part of the equation is the cost of treatment. A long turnaround time to results usually means placing the patient on any available treatment, which is not necessarily the best option. If a suboptimal treatment decision is made and subsequently a treatment change needs to be forced, the patient will pay for it in terms of outcomes. The health care system will probably also bear additional costs because those patients usually experience more side effects, which means rehospitalization costs and a prolonged process.

Fiona Nohilly, can you comment on the movement to in-house and how you look at the total cost of performing the test for the benefit of patients?

Fiona Nohilly, senior manager, product marketing, Americas regional marketing, Illumina: We are thinking about the total cost of ownership from sample and library preparation through sequencing and analysis. Since we last met for this roundtable, we have launched three new platforms.

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