P579: Multidimensional utility of genomic autopsy for infant mortality by Monica Wojcik, Casie Genetti, Malika Sud, Jill Madden, Kathleen Garvey, Ikeoluwa Osei-Owusu, Nicole Groussis, Sundos Al-Husayni, Pankaj Agrawal, Richard Goldstein, Heidi Rehm, Anne O'Donnell-Luria, Alan Beggs, Ingrid Holm

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P647: Improving rare disease diagnosis: Performance of an automated pipeline for genomic reanalysis by Christina Tse, Kaileigh Ahlquist, Matthew Welland, Paul de Fazio, Cas Simons, Lynn Pais, Giles Hall, Jeremiah Wander, Greg Smith, Laura Gauthier, Anne O'Donnell-Luria, Daniel MacArthur, Zornitza Stark, Heidi Rehm, Kaitlin Samocha

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P630: ClinGen curation of ClinVar: Improving a critical community resource* by Heidi Rehm, Julie Ratliff, Pamela Robertson, Danielle Azzariti, Larry Babb, Anabella Popiel, Audrey O’Neill, Vanessa Gitau, Ryan Webb, Eric Coleman, Kyle Ferriter, Terry O’Neill, Kuljeet Kaur, Shanmuga Chitipiralla, Chao Chen, Baoshan Gu, Jinpeng Yang, Steven Harrison, Erin Riggs, Marina DiStefano, Melissa Landrum

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O28: GREGoR: Accelerating genomics for rare diseases by Moez Dawood, Ben Heavner, Marsha Wheeler, Rachel Ungar, Jonathan LoTempio, Laurens Wiel, Seth Berger, Jonathan Bernstein, Jessica Chong, Emmanuèle Délot, Evan Eichler, Richard Gibbs, James Lupski, Ali Shojaie, Michael Talkowski, Chia-Lin Wei, Matthew Wheeler, Eric Vilain, Fritz Sedlazeck, Danny Miller, Casey Gifford, Susanne May, Heidi Rehm, Anne O'Donnell-Luria, Jennifer Posey, Lisa Chadwick, Michael Bamshad, Stephen Montgomery

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