The detection of cancer in the body, particularly early in its progression, can provide life-saving information for subsequent treatment. Researchers are now demonstrating that increases in the speed, accuracy, and resolution of next-generation sequencing (NGS) have made it possible to sequence minute amounts of DNA from scarce and rare samples, such as circulating cancer cells from liquid biopsies or archival tissue in formalin-fixed paraffin embedded (FFPE) samples. Taking this to the next level, NGS panels enable targeted sequencing of a small number of cancer-specific genes that can aid in quickly identifying and categorizing a particular cancer. This seminar will focus on the development and use of cancer detection panels for FFPE/liquid biopsy samples. Relying on their experience in both research and clinical settings, our panelists will discuss the challenges of designing, developing, analytically validating, and employing targeted NGS panels in translational research laboratories. The dramatic potential for future applications of NGS panels in a clinical setting will also be discussed.
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