Výsledky vyhledávání - McLean, Cory Y

Reducing Pervasive False-Positive Identical-by-Descent Segments Detected by Large-Scale Pedigree Analysis Autor Durand, Eric Y., Eriksson, Nicholas, McLean, Cory Y.

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GenomeWarp: an alignment-based variant coordinate transformation Autor McLean, Cory Y, Hwang, Yeongwoo, Poplin, Ryan, DePristo, Mark A

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Sequential regulatory activity prediction across chromosomes with convolutional neural networks Autor Kelley, David R., Reshef, Yakir A., Bileschi, Maxwell, Belanger, David, McLean, Cory Y., Snoek, Jasper

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Accurate, scalable cohort variant calls using DeepVariant and GLnexus Autor Yun, Taedong, Li, Helen, Chang, Pi-Chuan, Lin, Michael F, Carroll, Andrew, McLean, Cory Y

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PRISM offers a comprehensive genomic approach to transcription factor function prediction Autor Wenger, Aaron M., Clarke, Shoa L., Guturu, Harendra, Chen, Jenny, Schaar, Bruce T., McLean, Cory Y., Bejerano, Gill

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A Penile Spine/Vibrissa Enhancer Sequence Is Missing in Modern and Extinct Humans but Is Retained in Multiple Primates with Penile Spines and Sensory Vibrissae Autor Reno, Philip L., McLean, Cory Y., Hines, Jasmine E., Capellini, Terence D., Bejerano, Gill, Kingsley, David M.

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GREAT improves functional interpretation of cis-regulatory regions Autor McLean, Cory Y, Bristor, Dave, Hiller, Michael, Clarke, Shoa L, Schaar, Bruce T, Lowe, Craig B, Wenger, Aaron M, Bejerano, Gill

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DeepNull models non-linear covariate effects to improve phenotypic prediction and association power Autor McCaw, Zachary R., Colthurst, Thomas, Yun, Taedong, Furlotte, Nicholas A., Carroll, Andrew, Alipanahi, Babak, McLean, Cory Y., Hormozdiari, Farhad

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A population-specific reference panel for improved genotype imputation in African Americans Autor O’Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H., Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y.

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Human-specific loss of regulatory DNA and the evolution of human-specific traits Autor McLean, Cory Y., Reno, Philip L., Pollen, Alex A., Bassan, Abraham I., Capellini, Terence D., Guenther, Catherine, Indjeian, Vahan B., Lim, Xinhong, Menke, Douglas B., Schaar, Bruce T., Wenger, Aaron M., Bejerano, Gill, Kingsley, David M.

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An open resource for accurately benchmarking small variant and reference calls Autor Zook, Justin M., McDaniel, Jennifer, Olson, Nathan D., Wagner, Justin, Parikh, Hemang, Heaton, Haynes, Irvine, Sean A., Trigg, Len, Truty, Rebecca, McLean, Cory Y., De La Vega, Francisco M., Xiao, Chunlin, Sherry, Stephen, Salit, Marc

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Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology Autor Alipanahi, Babak, Hormozdiari, Farhad, Behsaz, Babak, Cosentino, Justin, McCaw, Zachary R., Schorsch, Emanuel, Sculley, D., Dorfman, Elizabeth H., Foster, Paul J., Peng, Lily H., Phene, Sonia, Hammel, Naama, Carroll, Andrew, Khawaja, Anthony P., McLean, Cory Y.

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Mutational Analysis Reveals the Origin and Therapy-driven Evolution of Recurrent Glioma Autor Johnson, Brett E., Mazor, Tali, Hong, Chibo, Barnes, Michael, Aihara, Koki, McLean, Cory Y., Fouse, Shaun D., Yamamoto, Shogo, Ueda, Hiroki, Tatsuno, Kenji, Asthana, Saurabh, Jalbert, Llewellyn E., Nelson, Sarah J., Bollen, Andrew W., Gustafson, W. Clay, Charron, Elise, Weiss, William A., Smirnov, Ivan V., Song, Jun S., Olshen, Adam B., Cha, Soonmee, Zhao, Yongjun, Moore, Richard A., Mungall, Andrew J., Jones, Steven J.M., Hirst, Martin, Marra, Marco A., Saito, Nobuhito, Aburatani, Hiroyuki, Mukasa, Akitake, Berger, Mitchel S., Chang, Susan M., Taylor, Barry S., Costello, Joseph F.

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Diagnosis of Parkinson’s disease on the basis of clinical–genetic classification: a population-based modelling study Autor Nalls, Mike A., McLean, Cory Y., Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J., Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T. Ryan, Nicolas, Aude, Keller, Margaux F., Molony, Cliona, Gibbs, J. Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S., Mapstone, Mark, Federoff, Howard J., Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M., Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G., Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G., Stone, David J., Ioannidis, John P. A., Singleton, Andrew B.

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Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease Autor Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana

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Quantifying penetrance in a dominant disease gene using large population control cohorts Autor Minikel, Eric Vallabh, Vallabh, Sonia M., Lek, Monkol, Estrada, Karol, Samocha, Kaitlin E., Sathirapongsasuti, J. Fah, McLean, Cory Y., Tung, Joyce Y., Yu, Linda P.C., Gambetti, Pierluigi, Blevins, Janis, Zhang, Shulin, Cohen, Yvonne, Chen, Wei, Yamada, Masahito, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Mizusawa, Hidehiro, Nakamura, Yosikazu, Kitamoto, Tetsuyuki, Collins, Steven J., Boyd, Alison, Will, Robert G., Knight, Richard, Ponto, Claudia, Zerr, Inga, Kraus, Theo F.J., Eigenbrod, Sabina, Giese, Armin, Calero, Miguel, de Pedro-Cuesta, Jesús, Haïk, Stéphane, Laplanche, Jean-Louis, Bouaziz-Amar, Elodie, Brandel, Jean-Philippe, Capellari, Sabina, Parchi, Piero, Poleggi, Anna, Ladogana, Anna, O'Donnell-Luria, Anne H., Karczewski, Konrad J., Marshall, Jamie L., Boehnke, Michael, Laakso, Markku, Mohlke, Karen L., Kähler, Anna, Chambert, Kimberly, McCarroll, Steven, Sullivan, Patrick F., Hultman, Christina M., Purcell, Shaun M., Sklar, Pamela, van der Lee, Sven J., Rozemuller, Annemieke, Jansen, Casper, Hofman, Albert, Kraaij, Robert, van Rooij, Jeroen G.J., Ikram, M. Arfan, Uitterlinden, André G., van Duijn, Cornelia M., Daly, Mark J., MacArthur, Daniel G.

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