Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Following publication of the original article [1], the authors reported an error in Additional file 1.
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BMC
2019-05-01
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| Series: | Genome Biology |
| Online Access: | http://link.springer.com/article/10.1186/s13059-019-1702-7 |
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doaj-d4bfc5d7f5e947398faeb9fc0c691b952020-11-25T03:36:45ZengBMCGenome Biology1474-760X2019-05-012011110.1186/s13059-019-1702-7Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A. Cheung0Xiaojian Shao1Andréanne Morin2Valérie Siroux3Tony Kwan4Bing Ge5Dylan Aïssi6Lu Chen7Louella Vasquez8Fiona Allum9Frédéric Guénard10Emmanuelle Bouzigon11Marie-Michelle Simon12Elodie Boulier13Adriana Redensek14Stephen Watt15Avik Datta16Laura Clarke17Paul Flicek18Daniel Mead19Dirk S. Paul20Stephan Beck21Guillaume Bourque22Mark Lathrop23André Tchernof24Marie-Claude Vohl25Florence Demenais26Isabelle Pin27Kate Downes28Hendrick G. Stunnenberg29Nicole Soranzo30Tomi Pastinen31Elin Grundberg32Department of Human Genetics, McGill UniversityDepartment of Human Genetics, McGill UniversityDepartment of Human Genetics, McGill UniversityTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced BiosciencesDepartment of Human Genetics, McGill UniversityDepartment of Human Genetics, McGill UniversityTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced BiosciencesDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome CampusDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome CampusDepartment of Human Genetics, McGill UniversityInstitute of Nutrition and Functional Foods (INAF), Laval UniversityGenetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris CitéMcGill University and Genome Quebec Innovation CentreMcGill University and Genome Quebec Innovation CentreMcGill University and Genome Quebec Innovation CentreDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome CampusEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome CampusEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome CampusEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome CampusDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome CampusUCL Cancer Institute, University College LondonUCL Cancer Institute, University College LondonDepartment of Human Genetics, McGill UniversityDepartment of Human Genetics, McGill UniversityQuébec Heart and Lung Institute, Laval UniversityInstitute of Nutrition and Functional Foods (INAF), Laval UniversityGenetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris CitéTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced BiosciencesDepartment of Haematology, University of Cambridge, Cambridge Biomedical CampusFaculty of Science, Department of Molecular Biology, Radboud UniversityDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome CampusDepartment of Human Genetics, McGill UniversityDepartment of Human Genetics, McGill UniversityFollowing publication of the original article [1], the authors reported an error in Additional file 1.http://link.springer.com/article/10.1186/s13059-019-1702-7 |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Warren A. Cheung Xiaojian Shao Andréanne Morin Valérie Siroux Tony Kwan Bing Ge Dylan Aïssi Lu Chen Louella Vasquez Fiona Allum Frédéric Guénard Emmanuelle Bouzigon Marie-Michelle Simon Elodie Boulier Adriana Redensek Stephen Watt Avik Datta Laura Clarke Paul Flicek Daniel Mead Dirk S. Paul Stephan Beck Guillaume Bourque Mark Lathrop André Tchernof Marie-Claude Vohl Florence Demenais Isabelle Pin Kate Downes Hendrick G. Stunnenberg Nicole Soranzo Tomi Pastinen Elin Grundberg |
| spellingShingle |
Warren A. Cheung Xiaojian Shao Andréanne Morin Valérie Siroux Tony Kwan Bing Ge Dylan Aïssi Lu Chen Louella Vasquez Fiona Allum Frédéric Guénard Emmanuelle Bouzigon Marie-Michelle Simon Elodie Boulier Adriana Redensek Stephen Watt Avik Datta Laura Clarke Paul Flicek Daniel Mead Dirk S. Paul Stephan Beck Guillaume Bourque Mark Lathrop André Tchernof Marie-Claude Vohl Florence Demenais Isabelle Pin Kate Downes Hendrick G. Stunnenberg Nicole Soranzo Tomi Pastinen Elin Grundberg Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome Genome Biology |
| author_facet |
Warren A. Cheung Xiaojian Shao Andréanne Morin Valérie Siroux Tony Kwan Bing Ge Dylan Aïssi Lu Chen Louella Vasquez Fiona Allum Frédéric Guénard Emmanuelle Bouzigon Marie-Michelle Simon Elodie Boulier Adriana Redensek Stephen Watt Avik Datta Laura Clarke Paul Flicek Daniel Mead Dirk S. Paul Stephan Beck Guillaume Bourque Mark Lathrop André Tchernof Marie-Claude Vohl Florence Demenais Isabelle Pin Kate Downes Hendrick G. Stunnenberg Nicole Soranzo Tomi Pastinen Elin Grundberg |
| author_sort |
Warren A. Cheung |
| title |
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| title_short |
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| title_full |
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| title_fullStr |
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| title_full_unstemmed |
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| title_sort |
correction to: functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome |
| publisher |
BMC |
| series |
Genome Biology |
| issn |
1474-760X |
| publishDate |
2019-05-01 |
| description |
Following publication of the original article [1], the authors reported an error in Additional file 1. |
| url |
http://link.springer.com/article/10.1186/s13059-019-1702-7 |
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