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

Genome Biology volume 20, Article number: 89 (2019) Cite this article

The Original Article was published on 10 March 2017

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.

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.

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Author information

Author notes

  1. Warren A. Cheung, Xiaojian Shao and Andréanne Morin contributed equally to this work.

Authors and Affiliations

  1. Department of Human Genetics, McGill University, Montreal, Quebec, Canada

    Warren A. Cheung, Xiaojian Shao, Andréanne Morin, Tony Kwan, Bing Ge, Fiona Allum, Guillaume Bourque, Mark Lathrop, Tomi Pastinen & Elin Grundberg

  2. McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada

    Warren A. Cheung, Xiaojian Shao, Andréanne Morin, Tony Kwan, Bing Ge, Fiona Allum, Marie-Michelle Simon, Elodie Boulier, Adriana Redensek, Guillaume Bourque, Mark Lathrop, Tomi Pastinen & Elin Grundberg

  3. Team of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced Biosciences, Grenoble, France

    Valérie Siroux, Dylan Aïssi & Isabelle Pin

  4. Department of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK

    Lu Chen, Louella Vasquez, Stephen Watt, Daniel Mead & Nicole Soranzo

  5. Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Long Road, Cambridge, CB2 0PT, UK

    Lu Chen, Kate Downes & Nicole Soranzo

  6. Institute of Nutrition and Functional Foods (INAF), Laval University, Québec, QC, G1V 0A6, Canada

    Frédéric Guénard & Marie-Claude Vohl

  7. Genetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France

    Emmanuelle Bouzigon & Florence Demenais

  8. European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK

    Avik Datta, Laura Clarke & Paul Flicek

  9. UCL Cancer Institute, University College London, 72 Huntley Street, London, WC1E 6BT, UK

    Dirk S. Paul & Stephan Beck

  10. Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Worts Causeway, Cambridge, CB1 8RN, UK

    Dirk S. Paul

  11. Québec Heart and Lung Institute, Laval University, Québec, QC, G1V 4G5, Canada

    André Tchernof

  12. Pédiatrie, Centre Hospitalier Universitaire (CHU) Grenoble Alpes, Grenoble, France

    Isabelle Pin

  13. National Health Service (NHS) Blood and Transplant, Cambridge Biomedical Campus, Long Road, Cambridge, CB2 0PT, UK

    Kate Downes

  14. Faculty of Science, Department of Molecular Biology, Radboud University, Nijmegen, 6525GA, The Netherlands

    Hendrick G. Stunnenberg

  15. British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke’s Hospital, Hills Road, Cambridge, CB2 0QQ, UK

    Nicole Soranzo

  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

    Nicole Soranzo

Authors
  1. Warren A. Cheung
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  2. Xiaojian Shao
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  3. Andréanne Morin
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  4. Valérie Siroux
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  5. Tony Kwan
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  6. Bing Ge
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  7. Dylan Aïssi
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  8. Lu Chen
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  9. Louella Vasquez
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  10. Fiona Allum
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  11. Frédéric Guénard
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  12. Emmanuelle Bouzigon
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  13. Marie-Michelle Simon
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  14. Elodie Boulier
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  15. Adriana Redensek
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  16. Stephen Watt
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  17. Avik Datta
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  18. Laura Clarke
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  19. Paul Flicek
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  20. Daniel Mead
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  21. Dirk S. Paul
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  22. Stephan Beck
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  23. Guillaume Bourque
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  24. Mark Lathrop
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  25. André Tchernof
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  26. Marie-Claude Vohl
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  27. Florence Demenais
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  28. Isabelle Pin
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  29. Kate Downes
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  30. Hendrick G. Stunnenberg
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  31. Nicole Soranzo
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  32. Tomi Pastinen
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  33. Elin Grundberg
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Corresponding authors

Correspondence to Tomi Pastinen or Elin Grundberg.

Additional file

Additional file 1

Description of MCC-Seq capture panel. This file contains: (1) summary of CpGs and genomic regions targeted by the MCC-Seq capture panel design (.xlsx Excel spreadsheet format), and (2) a list of the targeted regions (.bed text file). (ZIP 4405 kb)

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Open Access This 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.

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Cheung, W.A., Shao, X., Morin, A. et al. Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome. Genome Biol 20, 89 (2019). https://doi.org/10.1186/s13059-019-1702-7

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

Genome Biology

ISSN: 1474-760X

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