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Correction to: Relatively frequent switching of transcription start sites during cerebellar development Zhang, Peter; Dimont, Emmanuel; Ha, Thomas; Swanson, Douglas J; Itoh, Masayoshi; Kawaji, Hideya; Lassmann, Timo; Daub, Carsten O; Arner, Erik; Carninci, Piero; Hayashizaki, Yoshihide; Forrest, Alistair R R; Hide, Winston; Goldowitz, Dan Jan 11, 2018

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CORRECTION Open AccessCorrection to: Relatively frlaFAidItoh, Hideya Kawaji, Timo Lassmann, Carsten O. Daub,read and approved the final manuscript.The efforts of PZ, TH, DS and DG were supportedCentre for Life Science Technologies, Division ofon Ave, Boston,usetts Ave,ogies, RIKENLife Sciencee and DiagnosisThe University of6008, Australia.Zhang et al. BMC Genomics  (2018) 19:39 DOI 10.1186/s12864-017-4291-4Institute, Department of Medical Genetics, University of British Columbia, 950West 28th Avenue, Vancouver, BC V5Z 4H4, Canada8Department of Neuroscience, Sheffield Institute of TranslationalNeuroscience, University of Sheffield, Room B37 385a Glossop Road,Sheffield, South Yorkshire S10 2HQ, UK.* Correspondence:†Equal contributors1Centre for Molecular Medicine and Therapeutics, Child and Family Researchtal design and manuscript preparation. We thank F.Lucero Villegas for animal management. We thankM. Larouche, D. Rains and J. Boyle for technical sup-port. We thank Dora Pak and Anita Sham for man-agement support and Miroslav Hatas for systemsBiostatistics, Harvard School of Public Health, 655 HuntingtMA 02115, USA. 3Harvard Stem Cell Institute, 1350 MassachCambridge, MA 02138, USA. 4Division of Genomic TechnolOmics Science Center, Yokohama, Japan. 5RIKEN Center forTechnologies, Yokohama, Japan. 6RIKEN Preventive MedicinInnovation Program, Wako, Japan. 7Telethon Kids Institute,Western Australia, 100 Roberts Road, Subiaco, Subiaco, WAAcknowledgementsWe thank J. Yeung, J. Cairns, S. Tremblay, A. Poon,J. Wilking for support and suggestions on experimen-Genomic Technologies (from the MEXT, Japan).Author details1Centre for Molecular Medicine and Therapeutics, Child and Family ResearchInstitute, Department of Medical Genetics, University of British Columbia, 950West 28th Avenue, Vancouver, BC V5Z 4H4, Canada. 2Department ofand Diagnosis Innovation Program to YH and RIKENErik Arner, Piero Carninci, Yoshihide Hayashizaki andAlistair R. R. Forrest, as well as their affiliations.The following updates to Author contributions’, Acknowl-edgements and Funding have also been included below:New Author Contributions statementPZ, TH, DS and DG generated samples for the timeseries. MI and PC generated the CAGE libraries. YH,COD, ARRF and PC managed and organized the FAN-TOM5 project. ED, TL, HK, EA and PZ performed dataanalysis. PZ performed biological validation experiments.PZ, DG, ED and WH wrote the manuscript. The authorsCorrectionThe authors of the original article [1] would like torecognize the critical contribution of core members of theFANTOM5 Consortium, who played the critical role ofHeliScopeCAGE sequencing experiments, quality controlof tag reads and processing of the raw sequencing data.The revised author list includes authors Masayoshiof transcription start sitesdevelopmentPeter Zhang1†, Emmanuel Dimont2,3†, Thomas Ha1, DougTimo Lassmann4,5,7, Carsten O. Daub4,5, Erik Arner4,5, theYoshihide Hayashizaki4,6, Alistair R. R. Forrest4,5, Winston H© The Author(s). 2018 Open Access This articInternational License (http://creativecommonsreproduction in any medium, provided you gthe Creative Commons license, and indicate if( GenomeBC and National Institutes of Health, Nat-ural Sciences and Engineering Research Council ofCanada. FANTOM5 was made possible by a ResearchGrant for RIKEN Omics Science Center from MEXTto YH and a grant of the Innovative Cell Biology byInnovative Technology (Cell Innovation Program)from the MEXT, Japan to YH. It was also supportedby Research Grants for RIKEN Preventive Medicineequent switchingduring cerebellars J. Swanson1, Masayoshi Itoh4,5,6, Hideya Kawaji4,5,6,NTOM Consortium4,5, Piero Carninci4,5,e2,3,8 and Dan Goldowitz1*support. We would like to thank all members of theFANTOM5 consortium for contributing to generationof samples and analysis of the data-set and thankGeNAS for data production. We thank GenomeBC,National Institutes of Health, Natural Sciences andEngineering Research Council of Canada, NeuroDev-Net, MEXT Japan and University of British Columbiafor funding support.Fundingle is distributed under the terms of the Creative Commons Attribution, which permits unrestricted use, distribution, andive appropriate credit to the original author(s) and the source, provide a link tochanges were made. The Creative Commons Public Domain Dedication waiverro/1.0/) applies to the data made available in this article, unless otherwise stated.Received: 10 November 2017 Accepted: 10 November 2017Reference1. Zhang P, Dimont E, Ha T, Swanson DJ, Itoh M, Kawaji H, Lassman T, DaubCO, Arner E, the FANTOM Consortium, Carninci P, Hayashizaki Y, ForrestARR, Hide W, Goldowitz D. Relatively frequent switching of transcriptionstart sites during cerebellar development. BMC Genomics. 2017;18:461. et al. BMC Genomics  (2018) 19:39 Page 2 of 2


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