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The Somatic Genomic Landscape of Glioblastoma
Errata
miR-9a Minimizes the Phenotypic Impact of Genomic Diversity by Buffering a Transcription Factor Justin J. Cassidy, Aashish R. Jha, Diana M. Posadas, Ritika Giri, Koen J.T. Venken, Jingran Ji, Hongmei Jiang, Hugo J. Bellen, Kevin P. White, and Richard W. Carthew* *Correspondence: [email protected] http://dx.doi.org/10.1016/j.cell.2014.04.003
(Cell 155, 1556–1567; December 19, 2013) In the above article, we did not indicate a Sequence Read Archive (SRA) accession number for the DNA sequence data obtained to draw our conclusions. These data are available under the accession number SRP039006 at http://www.ncbi.nlm.nih.gov/sra/.
The Somatic Genomic Landscape of Glioblastoma Cameron W. Brennan,* Roel G.W. Verhaak, Aaron McKenna, Benito Campos, Houtan Noushmehr, Sofie R. Salama, Siyuan Zheng, Debyani Chakravarty, J. Zachary Sanborn, Samuel H. Berman, Rameen Beroukhim, Brady Bernard, Chang-Jiun Wu, Giannicola Genovese, Ilya Shmulevich, Jill Barnholtz-Sloan, Lihua Zou, Rahulsimham Vegesna, Sachet A. Shukla, Giovanni Ciriello, W.K. Yung, Wei Zhang, Carrie Sougnez, Tom Mikkelsen, Kenneth Aldape, Darell D. Bigner, Erwin G. Van Meir, Michael Prados, Andrew Sloan, Keith L. Black, Jennifer Eschbacher, Gaetano Finocchiaro, William Friedman, David W. Andrews, Abhijit Guha, Mary Iacocca, Brian P. O’Neill, Greg Foltz, Jerome Myers, Daniel J. Weisenberger, Robert Penny, Raju Kucherlapati, Charles M. Perou, D. Neil Hayes, Richard Gibbs, Marco Marra, Gordon B. Mills, Eric Lander, Paul Spellman, Richard Wilson, Chris Sander, John Weinstein, Matthew Meyerson, Stacey Gabriel, Peter W. Laird, David Haussler, Gad Getz, Lynda Chin,* and TCGA Research Network *Correspondence: [email protected] (C.W.B.), [email protected] (L.C.) http://dx.doi.org/10.1016/j.cell.2014.04.004
(Cell 155, 462–477; October 10, 2013) In the above article, we stated that our SNV mutations count included 5,379 silent, 3,901 missense, 831 nonsense, 360 splice-site, and 760 mutations resulting in a frame shift. One of these figures represents an error; the missense mutation count should read 13,901 and not 3,901. The underlying data as well as the rest of the text and figures reflect the correct mutation count (13,901).
Cell 157, 753, April 24, 2014 ª2014 Elsevier Inc. 753
miR-9a Minimizes the Phenotypic Impact of Genomic Diversity by Buffering a Transcription Factor Justin J. Cassidy, Aashish R. Jha, Diana M. Posadas, Ritika Giri, Koen J.T. Venken, Jingran Ji, Hongmei Jiang, Hugo J. Bellen, Kevin P. White, and Richard W. Carthew* *Correspondence: [email protected] http://dx.doi.org/10.1016/j.cell.2014.04.003
(Cell 155, 1556–1567; December 19, 2013) In the above article, we did not indicate a Sequence Read Archive (SRA) accession number for the DNA sequence data obtained to draw our conclusions. These data are available under the accession number SRP039006 at http://www.ncbi.nlm.nih.gov/sra/.
The Somatic Genomic Landscape of Glioblastoma Cameron W. Brennan,* Roel G.W. Verhaak, Aaron McKenna, Benito Campos, Houtan Noushmehr, Sofie R. Salama, Siyuan Zheng, Debyani Chakravarty, J. Zachary Sanborn, Samuel H. Berman, Rameen Beroukhim, Brady Bernard, Chang-Jiun Wu, Giannicola Genovese, Ilya Shmulevich, Jill Barnholtz-Sloan, Lihua Zou, Rahulsimham Vegesna, Sachet A. Shukla, Giovanni Ciriello, W.K. Yung, Wei Zhang, Carrie Sougnez, Tom Mikkelsen, Kenneth Aldape, Darell D. Bigner, Erwin G. Van Meir, Michael Prados, Andrew Sloan, Keith L. Black, Jennifer Eschbacher, Gaetano Finocchiaro, William Friedman, David W. Andrews, Abhijit Guha, Mary Iacocca, Brian P. O’Neill, Greg Foltz, Jerome Myers, Daniel J. Weisenberger, Robert Penny, Raju Kucherlapati, Charles M. Perou, D. Neil Hayes, Richard Gibbs, Marco Marra, Gordon B. Mills, Eric Lander, Paul Spellman, Richard Wilson, Chris Sander, John Weinstein, Matthew Meyerson, Stacey Gabriel, Peter W. Laird, David Haussler, Gad Getz, Lynda Chin,* and TCGA Research Network *Correspondence: [email protected] (C.W.B.), [email protected] (L.C.) http://dx.doi.org/10.1016/j.cell.2014.04.004
(Cell 155, 462–477; October 10, 2013) In the above article, we stated that our SNV mutations count included 5,379 silent, 3,901 missense, 831 nonsense, 360 splice-site, and 760 mutations resulting in a frame shift. One of these figures represents an error; the missense mutation count should read 13,901 and not 3,901. The underlying data as well as the rest of the text and figures reflect the correct mutation count (13,901).
Cell 157, 753, April 24, 2014 ª2014 Elsevier Inc. 753