Short‐term changes in cortical physiological arousal measured by electroencephalography during thalamic centromedian deep brain stimulation von Martin, Reese A., Cukiert, Arthur, Blumenfeld, Hal

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The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool von Flygare, Steven, Hernandez, Edgar Javier, Phan, Lon, Moore, Barry, Li, Man, Fejes, Anthony, Hu, Hao, Eilbeck, Karen, Huff, Chad, Jorde, Lynn, G Reese, Martin, Yandell, Mark

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Phevor Combines Multiple Biomedical Ontologies for Accurate Identification of Disease-Causing Alleles in Single Individuals and Small Nuclear Families von Singleton, Marc V., Guthery, Stephen L., Voelkerding, Karl V., Chen, Karin, Kennedy, Brett, Margraf, Rebecca L., Durtschi, Jacob, Eilbeck, Karen, Reese, Martin G., Jorde, Lynn B., Huff, Chad D., Yandell, Mark

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VAAST 2.0: Improved Variant Classification and Disease-Gene Identification Using a Conservation-Controlled Amino Acid Substitution Matrix von Hu, Hao, Huff, Chad D., Moore, Barry, Flygare, Steven, Reese, Martin G., Yandell, Mark

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An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases von Owen, Mallory J., Lefebvre, Sebastien, Hansen, Christian, Kunard, Chris M., Dimmock, David P., Smith, Laurie D., Scharer, Gunter, Mardach, Rebecca, Willis, Mary J., Feigenbaum, Annette, Niemi, Anna-Kaisa, Ding, Yan, Van Der Kraan, Luca, Ellsworth, Katarzyna, Guidugli, Lucia, Lajoie, Bryan R., McPhail, Timothy K., Mehtalia, Shyamal S., Chau, Kevin K., Kwon, Yong H., Zhu, Zhanyang, Batalov, Sergey, Chowdhury, Shimul, Rego, Seema, Perry, James, Speziale, Mark, Nespeca, Mark, Wright, Meredith S., Reese, Martin G., De La Vega, Francisco M., Azure, Joe, Frise, Erwin, Rigby, Charlene Son, White, Sandy, Hobbs, Charlotte A., Gilmer, Sheldon, Knight, Gail, Oriol, Albert, Lenberg, Jerica, Nahas, Shareef A., Perofsky, Kate, Kim, Kyu, Carroll, Jeanne, Coufal, Nicole G., Sanford, Erica, Wigby, Kristen, Weir, Jacqueline, Thomson, Vicki S., Fraser, Louise, Lazare, Seka S., Shin, Yoon H., Grunenwald, Haiying, Lee, Richard, Jones, David, Tran, Duke, Gross, Andrew, Daigle, Patrick, Case, Anne, Lue, Marisa, Richardson, James A., Reynders, John, Defay, Thomas, Hall, Kevin P., Veeraraghavan, Narayanan, Kingsmore, Stephen F.

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Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding von McKernan, Kevin Judd, Peckham, Heather E, Costa, Gina L, McLaughlin, Stephen F, Fu, Yutao, Tsung, Eric F, Clouser, Christopher R, Duncan, Cisyla, Ichikawa, Jeffrey K, Lee, Clarence C, Zhang, Zheng, Ranade, Swati S, Dimalanta, Eileen T, Hyland, Fiona C, Sokolsky, Tanya D, Zhang, Lei, Sheridan, Andrew, Fu, Haoning, Hendrickson, Cynthia L, Li, Bin, Kotler, Lev, Stuart, Jeremy R, Malek, Joel A, Manning, Jonathan M, Antipova, Alena A, Perez, Damon S, Moore, Michael P, Hayashibara, Kathleen C, Lyons, Michael R, Beaudoin, Robert E, Coleman, Brittany E, Laptewicz, Michael W, Sannicandro, Adam E, Rhodes, Michael D, Gottimukkala, Rajesh K, Yang, Shan, Bafna, Vineet, Bashir, Ali, MacBride, Andrew, Alkan, Can, Kidd, Jeffrey M, Eichler, Evan E, Reese, Martin G, De La Vega, Francisco M, Blanchard, Alan P

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Development of DNA Confirmatory and High-Risk Diagnostic Testing for Newborns Using Targeted Next-Generation DNA Sequencing von Bhattacharjee, Arindam, Sokolsky, Tanya, Wyman, Stacia K., Reese, Martin G., Puffenberger, Erik, Strauss, Kevin, Morton, Holmes, Parad, Richard B., Naylor, Edwin W.

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Response to Grosse et al von Kingsmore, Stephen F, Smith, Laurie D, Kunard, Chris M, Bainbridge, Matthew, Batalov, Sergey, Benson, Wendy, Blincow, Eric, Caylor, Sara, Chambers, Christina, Del Angel, Guillermo, Dimmock, David P, Ding, Yan, Ellsworth, Katarzyna, Feigenbaum, Annette, Frise, Erwin, Green, Robert C, Guidugli, Lucia, Hall, Kevin P, Hansen, Christian, Hobbs, Charlotte A, Kahn, Scott D, Kiel, Mark, Van Der Kraan, Lucita, Krilow, Chad, Kwon, Yong H, Madhavrao, Lakshminarasimha, Le, Jennie, Lefebvre, Sebastien, Mardach, Rebecca, Mowrey, William R, Oh, Danny, Owen, Mallory J, Powley, George, Scharer, Gunter, Shelnutt, Seth, Tokita, Mari, Mehtalia, Shyamal S, Oriol, Albert, Papadopoulos, Stavros, Perry, James, Rosales, Edwin, Sanford, Erica, Schwartz, Steve, Tran, Duke, Reese, Martin G, Wright, Meredith, Veeraraghavan, Narayanan, Wigby, Kristen, Willis, Mary J, Wolen, Aaron R, Defay, Thomas

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Population Genetic Inference from Personal Genome Data: Impact of Ancestry and Admixture on Human Genomic Variation von KIDD, Jeffrey M, GRAVEL, Simon, MCLAUGHLIN, Stephen F, PECKHAM, Heather E, OMBERG, Larsson, BORMANN CHUNG, Christina A, STANLEY, Sarah, PEARLSTEIN, Kevin, LEVANDOWSKY, Elizabeth, ACEVEDO-ACEVEDO, Suehelay, AUTON, Adam, KEINAN, Alon, BYRNES, Jake, ACUNA-ALONZO, Victor, BARQUERA-LOZANO, Rodrigo, CANIZALES-QUINTEROS, Samuel, ENG, Celeste, BURCHARD, Esteban G, RUSSELL, Archie, REYNOLDS, Andy, CLARK, Andrew G, REESE, Martin G, LINCOLN, Stephen E, MORENO-ESTRADA, Andres, BUTTE, Atul J, DE LA VEGA, Francisco M, BUSTAMANTE, Carlos D, MUSHAROFF, Shaila, BRYC, Katarzyna, DEGENHARDT, Jeremiah D, BRISBIN, Abra, SHETH, Vrunda, RONG CHEN

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A standard variation file format for human genome sequences von Reese, Martin G, Moore, Barry, Batchelor, Colin, Salas, Fidel, Cunningham, Fiona, Marth, Gabor T, Stein, Lincoln, Flicek, Paul, Yandell, Mark, Eilbeck, Karen

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Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins von Yandell, Mark, Moore, Barry, Salas, Fidel, Mungall, Chris, MacBride, Andrew, White, Charles, Reese, Martin G

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Using VAAST to Identify Disease‐Associated Variants in Next‐Generation Sequencing Data von Kennedy, Brett, Kronenberg, Zev, Hu, Hao, Moore, Barry, Flygare, Steven, Reese, Martin G., Jorde, Lynn B., Yandell, Mark, Huff, Chad

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P238: Discovery of the phenotypic landscape and mechanistic understanding of NAA10-related and NAA15-related neurodevelopmental syndromes, using mouse models and iPSCs von Lyon, Gholson, Vedaie, Marall, Beisheim, Travis, Park, Agnes, Marchi, Elaine, Gottlieb, Leah, Starr, Lois, Sandomirsky, Katherine, Cheng, Hanyin, Preddy, Isabelle, Tseng, Marcellus, Li, Quan, Wang, Kai, Gavin, Maureen, Amble, Karen, Marmorstein, Ronen, Herr-Israel, Ellen, Harpell, Randie, Nashat, Melissa, Ma, Ning, Belbachir, Nadjet, Wu, Joseph, Hsieh, Tzung-Chien, Krawitz, Peter, Rope, Alan, Monsma, Frederick, Wesely, Josephine, Chen, Yu-Ren, Hunter, Christopher, Bauer, Lauren, Rusielewicz, Tom, Kneeland, Stephen, Lutz, Cat, Snow, Kathy, Murray, Steve, Gropman, Andrea, Whitehead, Matthew, Garcia, Andrew, Inusa, Fatima, Longo, Joseph, Fleischer, Nicole, Bolton, David, Reese, Martin, Hu, Yu

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Dual nature of strongly correlated 5f electrons von Zwicknagl, Gertrud, Reese, Martin

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EGASP: collaboration through competition to find human genes von Guigó, Roderic, Reese, Martin G

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EGASP: the human ENCODE Genome Annotation Assessment Project von Guigó, Roderic, Flicek, Paul, Abril, Josep F, Reymond, Alexandre, Lagarde, Julien, Denoeud, France, Antonarakis, Stylianos, Ashburner, Michael, Bajic, Vladimir B, Birney, Ewan, Castelo, Robert, Eyras, Eduardo, Ucla, Catherine, Gingeras, Thomas R, Harrow, Jennifer, Hubbard, Tim, Lewis, Suzanna E, Reese, Martin G

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Annotating eukaryote genomes von Lewis, Suzanna, Ashburner, Michael, Reese, Martin G

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Natural Language Processing with Java: Techniques for Building Machine Learning and Neural Network Models for NLP von M. Reese, Richard, Bhatia, AshishSingh

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EGASP: Introduction von Reese, Martin G, Guigó, Roderic

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Java for data science: examine the techniques and Java tools supporting the growing field of data science von Reese, Richard M, Reese, Jennifer L

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