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BMC Genomics. 2018 Jan 11;19(1):39. doi: 10.1186/s12864-017-4291-4.

Correction to: Relatively frequent switching of transcription start sites during cerebellar development.

Author information

1
Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Department of Medical Genetics, University of British Columbia, 950 West 28th Avenue, Vancouver, BC, V5Z 4H4, Canada.
2
Department of Biostatistics, Harvard School of Public Health, 655 Huntington Ave, Boston, MA, 02115, USA.
3
Harvard Stem Cell Institute, 1350 Massachusetts Ave, Cambridge, MA, 02138, USA.
4
Division of Genomic Technologies, RIKEN Omics Science Center, Yokohama, Japan.
5
RIKEN Center for Life Science Technologies, Yokohama, Japan.
6
RIKEN Preventive Medicine and Diagnosis Innovation Program, Wako, Japan.
7
Telethon Kids Institute, The University of Western Australia, 100 Roberts Road, Subiaco, Subiaco, WA, 6008, Australia.
8
Department of Neuroscience, Sheffield Institute of Translational Neuroscience, University of Sheffield, Room B37 385a Glossop Road, Sheffield, South Yorkshire, S10 2HQ, UK.
9
Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Department of Medical Genetics, University of British Columbia, 950 West 28th Avenue, Vancouver, BC, V5Z 4H4, Canada. dang@cmmt.ubc.ca.

Abstract

The authors of the original article [1] would like to recognize the critical contribution of core members of the FANTOM5 Consortium, who played the critical role of HeliScopeCAGE sequencing experiments, quality control of tag reads and processing of the raw sequencing data.

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