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ccfDNA In the Lab: Optimizing Purification for Sequencing

ccfDNA Webinar Series: The Basics and Beyond

Circulating cell-free DNA (ccfDNA) can be used to monitor tumor burden and monitor disease progress.

In this part 3 of 3 ccfDNA webinars, Dr. Gulley discusses variables important to isolating high-quality ccfDNA from plasma samples including anticoagulant, plasma volume and storage length and conditions.

Review Part 1 & 2

Part 1 - ccfDNA 101: Emerging Trends in Oncology Research
Part 2 - ccfDNA Workflows: Honing in on the Target

Circulating cell-free DNA assays serve to monitor tumor burden and to track clonal evolution, including emerging drug resistance clones. Among the pre-analytic variables important for assuring high quality sequencing results on plasma DNA are choice of anticoagulant, input plasma volume, extraction chemistry, and the duration and storage conditions of blood before blood is processed to separate plasma. Interfering substances or processes may include hemolysis, leukocyte lysis, and nucleases. Assay validation resources can help in assay design and experimental design to optimize sensitivity, specificity, linearity and reproducibility of sequencing results. Controls, calibrators, and quality checks are valuable tools to demonstrate assays perform as expected. The adverse impact of tumor heterogeneity on tissue-based genomic profiles may be overcome, in part, by testing plasma that may yield a more global or systemic portrait of tumor clones and emerging subclones. Monitoring patients in serial plasma tests performed over time may be more informative than test results at a single timepoint. Ongoing research continues to reveal the utility of plasma DNA as a tool to enhance early diagnosis, tumor classification, and patient response to therapeutic interventions.

Click here to register for 12pm CDT / 1pm EDT / 10am PDT

Click here to register for 2:30pm London / 3:30pm Amsterdam

Click here to register for 12pm Singapore / 2pm Sydney / 1pm Seoul

12 June 2018

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