Результати пошуку - Cory Y. McLean
- Показ 1 - 20 результатів із 22
- На наступну сторінку
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1
Reducing Pervasive False-Positive Identical-by-Descent Segments Detected by Large-Scale Pedigree Analysis за авторством Éric Durand, Nicholas Eriksson, Cory Y. McLean
Опубліковано 2014Artigo -
2
Improving Phenotypic Measurements in High-Content Imaging Screens за авторством D. Michael Ando, Cory Y. McLean, Marc Berndl
Опубліковано 2017Pré-impressão -
3
Accurate, scalable cohort variant calls using DeepVariant and GLnexus за авторством Taedong Yun, Helen Li, Pi-Chuan Chang, Michael Lin, Andrew Carroll, Cory Y. McLean
Опубліковано 2020Artigo -
4
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5
GREAT improves functional interpretation of cis-regulatory regions за авторством Cory Y. McLean, Dave Bristor, Michael Hiller, Shoa L. Clarke, Bruce T. Schaar, Craig B. Lowe, Aaron M. Wenger, Gill Bejerano
Опубліковано 2010Artigo -
6
DeepNull models non-linear covariate effects to improve phenotypic prediction and association power за авторством Zachary R. McCaw, Thomas Colthurst, Taedong Yun, Nicholas A. Furlotte, Andrew Carroll, Babak Alipanahi, Cory Y. McLean, Farhad Hormozdiari
Опубліковано 2022Artigo -
7
A deep learning approach to pattern recognition for short DNA sequences за авторством Akosua Busia, George E. Dahl, Clara Fannjiang, David H. Alexander, Elizabeth H. Dorfman, Ryan Poplin, Cory Y. McLean, Pi-Chuan Chang, Mark A. DePristo
Опубліковано 2018Pré-impressão -
8
Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials за авторством Justin M. Zook, Jennifer McDaniel, Hemang Parikh, Haynes Heaton, Sean A. Irvine, Len Trigg, Rebecca Truty, Cory Y. McLean, Francisco M. De La Vega, Chunlin Xiao, Stephen T. Sherry, Marc Salit
Опубліковано 2018Pré-impressão -
9
Accurate human genome analysis with Element Avidity sequencing за авторством Andrew Carroll, Alexey Kolesnikov, Daniel E. Cook, Lucas Brambrink, Kelly Wiseman, Sophie Billings, Semyon Kruglyak, Bryan R. Lajoie, June Zhao, Shawn Levy, Cory Y. McLean, Kishwar Shafin, Maria Nattestad, Pi-Chuan Chang
Опубліковано 2023Pré-impressão -
10
Longitudinal fundus imaging and its genome-wide association analysis provide evidence for a human retinal aging clock за авторством Sara Ahadi, Kenneth A. Wilson, Boris Babenko, Cory Y. McLean, Drew Bryant, Orion Pritchard, Ajay Kumar, Enrique M. Carrera, Ricardo Lamy, Jay M. Stewart, Avinash V. Varadarajan, Marc Berndl, Pankaj Kapahi, Ali Bashir
Опубліковано 2023Artigo -
11
Human-specific loss of regulatory DNA and the evolution of human-specific traits за авторством Cory Y. McLean, Philip L. Reno, Alex A. Pollen, Abraham I. Bassan, Terence D. Capellini, Catherine Guenther, Vahan B. Indjeian, Xinhong Lim, Douglas B. Menke, Bruce T. Schaar, Aaron M. Wenger, Gill Bejerano, David M. Kingsley
Опубліковано 2011Artigo -
12
Creating a universal SNP and small indel variant caller with deep neural networks за авторством Ryan Poplin, Pi-Chuan Chang, David H. Alexander, Scott Schwartz, Thomas Colthurst, Alexander Ku, Dan Newburger, Jojo Dijamco, Nam V. Nguyen, Pegah Tootoonchi Afshar, Sam Gross, Lizzie Dorfman, Cory Y. McLean, Mark A. DePristo
Опубліковано 2016Pré-impressão -
13
A universal SNP and small-indel variant caller using deep neural networks за авторством Ryan Poplin, Pi-Chuan Chang, David H. Alexander, Scott Schwartz, Thomas Colthurst, Alexander Ku, Dan Newburger, Jojo Dijamco, Nam V. Nguyen, Pegah Tootoonchi Afshar, Sam Gross, Lizzie Dorfman, Cory Y. McLean, Mark A. DePristo
Опубліковано 2018Artigo -
14
An open resource for accurately benchmarking small variant and reference calls за авторством Justin M. Zook, Jennifer McDaniel, Nathan D. Olson, Justin Wagner, Hemang Parikh, Haynes Heaton, Sean A. Irvine, Len Trigg, Rebecca Truty, Cory Y. McLean, Francisco M. De La Vega, Chunlin Xiao, Stephen T. Sherry, Marc Salit
Опубліковано 2019Artigo -
15
Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology за авторством Babak Alipanahi, Farhad Hormozdiari, Babak Behsaz, Justin Cosentino, Zachary R. McCaw, Emanuel Schorsch, D. Sculley, Elizabeth H. Dorfman, Paul J. Foster, Lily H. Peng, Sonia Phene, Naama Hammel, Andrew Carroll, Anthony P. Khawaja, Cory Y. McLean
Опубліковано 2021Artigo -
16
Machine learning guided aptamer refinement and discovery за авторством Ali Bashir, Qin Yang, Jinpeng Wang, Stephan Hoyer, Wen-Chuan Chou, Cory Y. McLean, Geoff Davis, Qiang Gong, Zan Armstrong, Junghoon Jang, Hui Kang, Annalisa Pawlosky, Alexander P. Scott, George E. Dahl, Marc Berndl, Michelle Dimon, B. Scott Ferguson
Опубліковано 2021Artigo -
17
Unsupervised representation learning on high-dimensional clinical data improves genomic discovery and prediction за авторством Taedong Yun, Justin Cosentino, Babak Behsaz, Zachary R. McCaw, Davin Hill, Robert Luben, Dongbing Lai, John Bates, Howard H. Yang, Tae‐Hwi Schwantes‐An, Yuchen Zhou, Anthony P. Khawaja, Andrew Carroll, Brian D. Hobbs, Michael H. Cho, Cory Y. McLean, Farhad Hormozdiari
Опубліковано 2024Artigo -
18
Mutational Analysis Reveals the Origin and Therapy-Driven Evolution of Recurrent Glioma за авторством Brett Johnson, Tali Mazor, Chibo Hong, Michael J. Barnes, Koki Aihara, Cory Y. McLean, Shaun D. Fouse, Shogo Yamamoto, Hiroki Ueda, Kenji Tatsuno, Saurabh Asthana, Llewellyn E. Jalbert, Sarah J. Nelson, Andrew W. Bollen, W. Clay Gustafson, Elise Charron, William A. Weiss, Ivan Smirnov, Jun S. Song, Adam B. Olshen, Soonmee Cha, Yongjun Zhao, Richard A. Moore, Andrew J. Mungall, Steven J.M. Jones, Martin Hirst, Marco A. Marra, Nobuhito Saito, Hiroyuki Aburatani, Akitake Mukasa, Mitchel S. Berger, Susan M. Chang, Barry S. Taylor, J Costello
Опубліковано 2013Artigo -
19
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study за авторством Mike A. Nalls, Cory Y. McLean, Jacqueline Rick, Shirley Eberly, Samantha J. Hutten, Katrina Gwinn, Margaret Sutherland, María Martínez, Peter Heutink, Nigel Williams, John Hardy, Thomas Gasser, Alexis Brice, T. Ryan Price, Aude Nicolas, Margaux F. Keller, Cliona Molony, J. Raphael Gibbs, Alice Chen‐Plotkin, EunRan Suh, Christopher Letson, Massimo S. Fiandaca, Mark Mapstone, Howard J. Federoff, Alastair Noyce, Huw R. Morris, Vivianna M. Van Deerlin, Daniel Weintraub, Cyrus P. Zabetian, Dena G. Hernandez, Suzanne Lesage, Meghan Mullins, Emily Drabant Conley, Carrie A. M. Northover, Mark Frasier, Kenneth Marek, Aaron Day-Williams, David J. Stone, John P. A. Ioannidis, Andrew Singleton
Опубліковано 2015Artigo -
20
A population-specific reference panel for improved genotype imputation in African Americans за авторством Jared O’Connell, Taedong Yun, Meghan E. Moreno, Helen Li, Nadia K. Litterman, Alexey Kolesnikov, Elizabeth S. Noblin, Pi-Chuan Chang, Anjali J. Shastri, Elizabeth H. Dorfman, Suyash Shringarpure, Stella Aslibekyan, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Pooja Gandhi, Karl Heilbron, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Joanna L. Mountain, Priyanka Nandakumar, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Janie F. Shelton, Jingchunzi Shi, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna Wong, Adam Auton, Andrew Carroll, Cory Y. McLean
Опубліковано 2021Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Gene
Genetics
Computer science
Computational biology
Artificial intelligence
Genome
Genotype
Single-nucleotide polymorphism
Machine learning
1000 Genomes Project
Genomics
Human genome
Mathematics
Medicine
Data mining
Genome-wide association study
Mutation
Phenotype
Statistics
Biochemistry
Bioinformatics
Convolutional neural network
DNA sequencing
Deep learning
Disease
Evolutionary biology
Exome sequencing
Imputation (statistics)
Indel