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  • Correction
  • Open Access

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

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Contributed equally
Genome Biology201920:89

https://doi.org/10.1186/s13059-019-1702-7

  • Received: 25 April 2019
  • Accepted: 25 April 2019
  • Published:

The original article was published in Genome Biology 2017 18:50

Correction to: Genome Biol

https://doi.org/10.1186/s13059-017-1173-7

Following publication of the original article [1], the authors reported an error in Additional file 1. The updated Additional file 1 is given below.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Human Genetics, McGill University, Montreal, Quebec, Canada
(2)
McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada
(3)
Team of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced Biosciences, Grenoble, France
(4)
Department of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK
(5)
Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Long Road, Cambridge, CB2 0PT, UK
(6)
Institute of Nutrition and Functional Foods (INAF), Laval University, Québec, QC, G1V 0A6, Canada
(7)
Genetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France
(8)
European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK
(9)
UCL Cancer Institute, University College London, 72 Huntley Street, London, WC1E 6BT, UK
(10)
Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Worts Causeway, Cambridge, CB1 8RN, UK
(11)
Québec Heart and Lung Institute, Laval University, Québec, QC, G1V 4G5, Canada
(12)
Pédiatrie, Centre Hospitalier Universitaire (CHU) Grenoble Alpes, Grenoble, France
(13)
National Health Service (NHS) Blood and Transplant, Cambridge Biomedical Campus, Long Road, Cambridge, CB2 0PT, UK
(14)
Faculty of Science, Department of Molecular Biology, Radboud University, Nijmegen, 6525GA, The Netherlands
(15)
British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke’s Hospital, Hills Road, Cambridge, CB2 0QQ, UK
(16)
The National Institute for Health Research Blood and Transplant Unit (NIHR BTRU) in Donor Health and Genomics, University of Cambridge, Strangeways Research Laboratory, Wort’s Causeway, Cambridge, CB1 8RN, UK

Reference

  1. Cheung, et al. Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome. Genome Biol. 2017;18:50. https://doi.org/10.1186/s13059-017-1173-7.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© The Author(s). 2019

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