P485: Evaluating novel dosage sensitivity predictors for inclusion in the classification of recurrent copy number variants by John Herriges, Cassandra Runke, Zoe Lewis, Lucilla Pizzo, Bradley Coe, Laura Conlin, Benjamin Hilton, Brynn Levy, Andrea Vaags, Shulin Zhang, Christa Martin, Erica Andersen

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P576: Recalibration of scoring metrics to assess the pathogenicity of constitutional copy number variants (CNVs)* by Emily Spector, Erica Andersen, John Herriges, Anne Higgins, Brynn Levy, Ludmila Matyakhina, Christa Martin, Daniel Pineda-Alvarez, Lina Shao, Shashirekha Shetty, Andrea Vaags, Erik Thorland, Sung-Hae Kang, Chelsea Lowther, Dominic McMullan, Erin Riggs

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P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN) by Lauren Hughes, Kirsten Farncombe, Michelle Brazas, Melyssa Aronson, Kathleen Bell, Brandon Chan, Andrea Eisen, Harriet Feilotter, Bailey Gallinger, Jordan Lerner-Ellis, David Malkin, Ellen MacDougall, Steven Narod, Karen Panabaker, Trevor Pugh, Sarah Sawyer, Alison Rusnak, Andrea Vaags, Laszlo Radvanyi, Lincoln Stein, Raymond Kim

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A Pan-Canadian Validation Study for the Detection of EGFR T790M Mutation Using Circulating Tumor DNA From Peripheral Blood by Shamini Selvarajah, PhD, Sophie Plante, MSc, Marsha Speevak, PhD, Andrea Vaags, PhD, Darren Hamelinck, MSc, Martin Butcher, MSc, Elizabeth McCready, PhD, Daria Grafodatskaya, PhD, Normand Blais, MD, Danh Tran-Thanh, MD, Xiaoduan Weng, MD, Rami Nassabein, MD, Wenda Greer, PhD, Ryan N. Walton, MPH, Bryan Lo, MD, Doug Demetrick, MD, Stephanie Santos, BSc, Bekim Sadikovic, PhD, Xiao Zhang, BSc, MSc, Tong Zhang, MD, Tara Spence, PhD, Tracy Stockley, PhD, Harriet Feilotter, PhD, Philippe Joubert, MD, PhD

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