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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Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial von Kingsmore, Stephen F., Wright, Meredith, Olsen, Lauren, Schultz, Brandan, Protopsaltis, Liana, Averbuj, Dan, Blincow, Eric, Carroll, Jeanne, Caylor, Sara, Defay, Thomas, Ellsworth, Katarzyna, Feigenbaum, Annette, Gover, Mia, Guidugli, Lucia, Hansen, Christian, Van Der Kraan, Lucita, Kunard, Chris M., Kwon, Hugh, Madhavrao, Lakshminarasimha, Leipzig, Jeremy, Liang, Yupu, Mardach, Rebecca, Mowrey, William R., Nguyen, Hung, Niemi, Anna-Kaisa, Oh, Danny, Saad, Muhammed, Scharer, Gunter, Schleit, Jennifer, Mehtalia, Shyamal S., Sanford, Erica, Smith, Laurie D., Willis, Mary J., Wigby, Kristen, Reimers, Rebecca

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Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection von Kingsmore, Stephen F., Wright, Meredith, Smith, Laurie D., Liang, Yupu, Mowrey, William R., Protopsaltis, Liana, Bainbridge, Matthew, Baker, Mei, Batalov, Sergey, Blincow, Eric, Cao, Bryant, Caylor, Sara, Chambers, Christina, Ellsworth, Katarzyna, Feigenbaum, Annette, Frise, Erwin, Guidugli, Lucia, Hall, Kevin P., Hansen, Christian, Kiel, Mark, Van Der Kraan, Lucita, Krilow, Chad, Kwon, Hugh, Madhavrao, Lakshminarasimha, Lefebvre, Sebastien, Leipzig, Jeremy, Mardach, Rebecca, Moore, Barry, Oh, Danny, Olsen, Lauren, Ontiveros, Eric, Owen, Mallory J., Reimers, Rebecca, Scharer, Gunter, Schleit, Jennifer, Shelnutt, Seth, Mehtalia, Shyamal S., Oriol, Albert, Sanford, Erica, Schwartz, Steve, Wigby, Kristen, Willis, Mary J., Yandell, Mark, Kunard, Chris M., Defay, Thomas

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