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This is a recording of a session from AMP Europe 2018 meeting in Rotterdam. Purchase the entire AMP Europe 2018 Recordings for a significant discount!
In 2017, AMP partnered with various stakeholders to develop and publish two related published guideline manuscripts in The Journal for Molecular Diagnostics: 1) Guidelines for Validation of Next Generation Sequencing (NGS)-based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists and 2) Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. This session will be a discussion of how the guidelines were developed and will provide practical case-based implementation advice for laboratories both currently performing somatic NGS and those considering bringing these technologies into their laboratories.
Practice Guidelines for Validation, Interpretation and Reporting of NGS-Based Oncology Tests
Marina N. Nikiforova, MD (Pittsburgh, USA)
Objectives:
- Discuss key points of the guideline for validation of NGS-based oncology tests.
- Discuss key points of the guideline for the classification, interpretation, and reporting of somatic sequence variants in NGS-based oncology panels.
- Evaluate utility of these guidelines for development, validation, interpretation and reporting of the laboratory developed NGS tests using clinical case scenarios.
Duration: 0.75 hr
Recording Date: May 1, 2018
Last day to purchase: December 31, 2021
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