P156: Genomic disease contribution for unknown causes of infant mortality via genome sequencing of newborn dried blood spots and semiautomated interpretation von Ontiveros, Eric, Protopsaltis, Liana, Baer, Rebecca, Bainbridge, Matthew, Cao, Bryant, Ding, Yan, Ellsworth, Katarzyna (Kasia), Forero, Laura, Frise, Erwin, Guidugli, Lucia, Kwon, YongHyun, Le, Jennie, Oltman, Scott, Owen, Mallory, Kobayashi, Erica Sanford, Van Der Kraan, Lucita, Wright, Meredith, Yandell, Mark, Jelliffe-Pawlowski, Laura, Bandoli, Gretchen, Chambers, Christina, Kingsmore, Stephen

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P146: BeginNGS, an artificial intelligence-enabled genome sequencing system for newborn screening of 409 childhood genetic disorders von Schleit, Jennifer, Wright, Meredith, Olsen, Lauren, Blincow, Eric, Caylor, Sara, Chambers, Christina, Angel, Guillermo del, Ellsworth, Katarzyna (Kasia), Feigenbaum, Annette, Frise, Erwin, Guidugli, Lucia, Hall, Kevin, Hansen, Christian, Hobbs, Charlotte, Kiel, Mark, Krilow, Chad, Kunard, Chris, Kwon, YongHyun, Madhavrao, Rao, Mehtalia, Shyamal, Mowrey, William, Le, Jennie, Leipzig, Jeremy, Liang, Yupu, Mardach, Rebecca, Oh, Danny, Owen, Mallory, Protopsaltis, Liana, Kobayashi, Erica Sanford, Scharer, Gunter, Schultz, Brandon, Shelnutt, Seth, Smith, Laurie, Tran, Duke, Van Der Kraan, Lucita, Wigby, Kristen, Willis, Mary, Wolen, Aaron, Yandell, Mark, Defay, Thomas, Kingsmore, Stephen

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OP039: Best practices for the interpretation and reporting of clinical genome sequencing von Austin-Tse, Chrissy, Jobanputra, Vaidehi, Perry, Denise, Bick, David, Taft, Ryan, Venner, Eric, Gibbs, Richard, Young, Ted, Barnett, Sarah, Belmont, John, Boczek, Nicole, Chowdhury, Shimul, Ellsworth, Katarzyna (Kasia), Guha, Saurav, Kulkarni, Shashikant, Marcou, Cherisse, Meng, Linyan, Murdock, David, Rehman, Atteeq, Spiteri, Elizabeth, Thomas-Wilson, Amanda, Kearney, Hutton, Rehm, Heidi

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