Computational refinement of post-translational modifications predicted from tandem mass spectrometry

by Chung, Clement, Liu, Jian, Emili, Andrew, Frey, Brendan J.
Published 2011

Classifying and segmenting microscopy images with deep multiple instance learning

by Kraus, Oren Z., Ba, Jimmy Lei, Frey, Brendan J.
Published 2016

Challenges in estimating percent inclusion of alternatively spliced junctions from RNA-seq data

by Kakaradov, Boyko, Xiong, Hui Yuan, Lee, Leo J, Jojic, Nebojsa, Frey, Brendan J
Published 2012

Deep learning of the tissue-regulated splicing code

by Leung, Michael K. K., Xiong, Hui Yuan, Lee, Leo J., Frey, Brendan J.
Published 2014

Transcriptional Profiling of Endocrine Cerebro-Osteodysplasia Using Microarray and Next-Generation Sequencing

by Lahiry, Piya, Lee, Leo J., Frey, Brendan J., Rupar, C. Anthony, Siu, Victoria M., Blencowe, Benjamin J., Hegele, Robert A.
Published 2011

AVISPA: a web tool for the prediction and analysis of alternative splicing

by Barash, Yoseph, Vaquero-Garcia, Jorge, González-Vallinas, Juan, Xiong, Hui Yuan, Gao, Weijun, Lee, Leo J, Frey, Brendan J
Published 2013

A generalizable pre-clinical research approach for orphan disease therapy

by Beaulieu, Chandree L, Samuels, Mark E, Ekins, Sean, McMaster, Christopher R, Edwards, Aled M, Krainer, Adrian R, Hicks, Geoffrey G, Frey, Brendan J, Boycott, Kym M, MacKenzie, Alex E
Published 2012

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

by Merico, Daniele, Zarrei, Mehdi, Costain, Gregory, Ogura, Lucas, Alipanahi, Babak, Gazzellone, Matthew J., Butcher, Nancy J., Thiruvahindrapuram, Bhooma, Nalpathamkalam, Thomas, Chow, Eva W. C., Andrade, Danielle M., Frey, Brendan J., Marshall, Christian R., Scherer, Stephen W., Bassett, Anne S.
Published 2015

The functional landscape of mouse gene expression

by Zhang, Wen, Morris, Quaid D, Chang, Richard, Shai, Ofer, Bakowski, Malina A, Mitsakakis, Nicholas, Mohammad, Naveed, Robinson, Mark D, Zirngibl, Ralph, Somogyi, Eszter, Laurin, Nancy, Eftekharpour, Eftekhar, Sat, Eric, Grigull, Jörg, Pan, Qun, Peng, Wen-Tao, Krogan, Nevan, Greenblatt, Jack, Fehlings, Michael, van der Kooy, Derek, Aubin, Jane, Bruneau, Benoit G, Rossant, Janet, Blencowe, Benjamin J, Frey, Brendan J, Hughes, Timothy R
Published 2004

Mutations in STAMBP, encoding a deubiquitinating enzyme, cause Microcephaly-Capillary Malformation syndrome

by McDonell, Laura M., Mirzaa, Ghayda M., Alcantara, Diana, Schwartzentruber, Jeremy, Carter, Melissa T., Lee, Leo J., Clericuzio, Carol L., Graham, John M., Morris-Rosendahl, Deborah J., Polster, Tilman, Acsadi, Gyula, Townshend, Sharron, Williams, Simon, Halbert, Anne, Isidor, Bertrand, Smyser, Christopher D., Paciorkowski, Alex R., Willing, Marcia, Woulfe, John, Das, Soma, Beaulieu, Chandree L., Marcadier, Janet, Geraghty, Michael T., Frey, Brendan J., Majewski, Jacek, Bulman, Dennis E., Dobyns, William B., O’Driscoll, Mark, Boycott, Kym M.
Published 2013

Genome-wide characteristics of de novo mutations in autism

by Yuen, Ryan KC, Merico, Daniele, Cao, Hongzhi, Pellecchia, Giovanna, Alipanahi, Babak, Thiruvahindrapuram, Bhooma, Tong, Xin, Sun, Yuhui, Cao, Dandan, Zhang, Tao, Wu, Xueli, Jin, Xin, Zhou, Ze, Liu, Xiaomin, Nalpathamkalam, Thomas, Walker, Susan, Howe, Jennifer L, Wang, Zhuozhi, MacDonald, Jeffrey R, Chan, Ada JS, D’Abate, Lia, Deneault, Eric, Siu, Michelle T, Tammimies, Kristiina, Uddin, Mohammed, Zarrei, Mehdi, Wang, Mingbang, Li, Yingrui, Wang, Jun, Wang, Jian, Yang, Huanming, Bookman, Matt, Bingham, Jonathan, Gross, Samuel S, Loy, Dion, Pletcher, Mathew, Marshall, Christian R, Anagnostou, Evdokia, Zwaigenbaum, Lonnie, Weksberg, Rosanna, Fernandez, Bridget A, Roberts, Wendy, Szatmari, Peter, Glazer, David, Frey, Brendan J, Ring, Robert H, Xu, Xun, Scherer, Stephen W
Published 2016