Barriers to care for women with low-grade endometrial cancer and morbid obesity: a qualitative study by Angela Han, Robin Hayeems, Deborah Robertson, Sari L Kives, Abheha Satkunaratnam, Sarah E Ferguson

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P383: The clinician-reported genetic testing utility InDEx in the NICU (C-GUIDETM-NICU): Quantifying genome-wide sequencing utility in neonatal critical care by Lena Dolman, Elise Poole, Joyce Yan, Stephanie Luca, Wendy Ungar, Lauren Chad, Martin Offringa, Robin Hayeems

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O54: Reimagining genetics service delivery: Genetics providers’ perspectives on the integration of digital tools into clinical practice by Whiwon Lee, Daena Hirjikaka, Sonya Grewal, Marc Clausen, Stephanie Luca, Angela Shaw, Yvonne Bombard, Robin Hayeems

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P479: The Clinician-reported Genetic testing Utility InDEx: A revised tool to quantify genome-wide sequencing utility in neonatal intensive care (C-GUIDE NICU) by Lena Dolman, Elise Poole, Joyce Yan, Stephanie Luca, Bowen Xiao, Wendy Ungar, Lauren Chad, Martin Offringa, Robin Hayeems

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P482: The clinical utility of genome-wide sequencing for rare disease: A multidimensional map by Robin Hayeems, Viji Venkataramanan, Katharine Fooks, Karen MacDonald, Trevor Seeger, Taila Hartley, Francois Bernier, Kym Boycott, Deborah Marshall

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P477: Barriers and facilitators to implementing genomic medicine: A scoping review of the global landscape* by Whiwon Lee, Joyce Yan, Katharine Fooks, Abby Tafler, Pooja Banglorewala, Melanie Barwick, Mark Dobrow, Jan Friedman, Christian Marshall, Robin Hayeems

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P543: Design and early findings from a mixed-methods study exploring the genomics era role of the medical geneticist in Canada by Michael Mackley, Kym Boycott, Shaimaa Helal, Lauren Chad, Gregory Costain, Ronald Cohn, Hanna Faghfoury, Aspasia Karalis, Roberto Mendoza-Londono, Robin Hayeems

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P373: Patients’ and parents’ perspectives on the use of digital tools to deliver genetic services by Daniel Assamad, Saumeh Saeedi, Sonya Grewal, Vedika Jha, Stephanie Luca, Marc Clausen, Angela Shaw, Whiwon Lee, Yvonne Bombard, Robin Hayeems, Genetics Navigator Study Team

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P547: The clinician-reported Genetic testing Utility InDEX (C-GUIDE): Establishing content validity for a new measure for sequencing-based newborn screening by Stephanie Luca, Katharine Fooks, Elise Poole, Amanda Pichini, Joanna Ziff, Katrina Stone, Bowen Xiao, Salma Shickh, David Bick, Pranesh Chakraborty, Wendy Ungar, Robin Hayeems

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P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape by Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, Wendy Ungar, James Stavropoulos, Lijia Huang, Viji Venkataramanan, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Robin Hayeems, Martin Somerville, Kym Boycott, Taila Hartley

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P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study by Vedika Jha, Saumeh Saeedi, Daniel Assamad, Sonya Grewal, Daena Hirjikaka, Whiwon Lee, Stephanie Luca, Angela Shaw, Robin Hayeems, Marc Clausen, Yvonne Bombard, Genetics Navigator Study Team

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P823: Insights and strategies for inclusive adolescent and young adult participation in genetics research by Tasha Wainstein, Courtney Cook, Daniel Assamad, Julia Heaton, Manraj Randhawa, David Yeung, Lauren Jennings, Robin Hayeems, Harpreet Chhina, Anthony Cooper, GenCOUNSEL. Study, Jehannine Austin, Alison Elliott

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Access to novel drugs and therapeutics for children and youth: Eliciting citizens' values to inform public funding decisions by Cindy L. Gauvreau, Lisa Wight, Mathushan Subasri, Antonia Palmer, Robin Hayeems, Alysha Croker, Julia Abelson, Brent Fraser, Yvonne Bombard, Charlotte Moore Hepburn, Michael G. Wilson, Avram Denburg

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P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing by Marc Clausen, Stephanie Luca, Emma Reble, Rita Kodida, Saumeh Saeedi, Daena Hirjikaka, Lauren Chad, Gregory Costain, Hanna Faghfoury, Josh Silver, Serena Shastri-Estrada, Maureen Smith, Robin Hayeems, Yvonne Bombard

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P873: “If you look for a problem, you’ll find one”: A qualitative study to understand why parents/adult patients decline secondary findings by Abigail Hansen, Stephanie Luca, Olivia Moran, Riyana Babul-Hirji, Joyce Yan, Katharine Fooks, Viji Venkataramanan, Wendy Ungar, Robin Hayeems, Secondary Findings Study Team, Elise Poole, Daniel Assamad, Pooja Banglorewala, Lydia Vermeer, Christian Marshall, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Olga Jarinova, Lynette Lau, Whiwon Lee, Lauren Badalato, Tugce Balci, Lauren Chad, Cara Inglese, Virginie Ladouceur, Michael Mackley, Chantal Morel, Julie Richer, Mark Tarnopolsky, Anita Villani, Laura Zahavich, Sarah Sawyer, Roberto Mendoza-Londono, Martin Somerville, Kym Boycott, Wendy Ungar, Robin Hayeems

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O05: A micro-costing and cost-effectiveness analysis of genome sequencing vs exome sequencing in pediatric rare diseases by Wendy Ungar, Vercancy Wu, Christian Marshall, Jackie Hwang, Robin Hayeems, Kate Tsiplova, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, Dimitri Stavropoulos, Viji Venkataramanan, Bowen Xiao, Sheena Li, Gregory Costain, Melanie Beaulieu Bergeron, Sarah Sawyer, Lynette Lau, Lijia Huang, Roberto Mendoza-Londono, Brian Smith, Edward Higginbotham, Martin Somerville, Kym Boycott

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P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study by Nicole Si Yan Liang, Gregory Costain, Alissa D'Gama, Amy McTague, Katherine Howell, Vann Chau, Sarah Mulhern, Annapurna Poduri, Ingrid Scheffer, Beth Sheidley, Meredith Curtis, Edward Higginbotham, Tayyaba Khan, Lyndsey McRae, Kimberly Wiltrout, Robin Hayeems, Puneet Jain, Sebastian Lunke, Christian Marshall, Lyn Chitty, Shira Rockowitz, Zornitza Stark, Susan White

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P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service by Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Taila Hartley, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Anna Pan, Jennifer Keating, Diana Matviychuk, Tamara Braid, Niri Carroll, Martin Somerville, Kym Boycott

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P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts by Elise Poole, Stephanie Luca, Daniel Assamad, Bowen Xiao, Joyce Yan, Pooja Banglorewala, Cheryl Xia, Wendy Ungar, Lesleigh Abbott, Linlea Armstrong, Patricia Birch, Kym Boycott, June Carroll, Lauren Chad, David Chitayat, Avram Denburg, Rebecca Deyell, Alison Elliott, Catherine Goudie, Anne-Marie Laberge, Melissa Maio, Iskra Peltekova, Becky Quinlan, Sarah Sawyer, Rachel Silver, Maureen Smith, Ronni Teitelbaum, Anita Villani, Tasha Wainstein, Robin Hayeems

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P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing by Katharine Fooks, Lydia Vermeer, Elise Poole, Stephanie Luca, Riyana Babul-Hirji, Lauren Chad, David Chitayat, Michael Mackley, Marci Schwartz, Wendy Ungar, Robin Hayeems, Secondary Findings Study Team, Joyce Yan, Abigail Hansen, Viji Venkataramanan, Daniel Assamad, Christian Marshall, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Olga Jarinova, Lynette Lau, Whiwon Lee, Lauren Badalato, Tugce Balci, Cara Inglese, Virginie Beausejour Ladouceur, Chantal Morel, Julie Richer, Mark Tarnopolsky, Anita Villani, Laura Zahavich, Olivia Moran, Sarah Sawyer, Roberto Mendoza-Londono, Martin Somerville, Kym Boycott

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