EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases.
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| Title: | EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases. |
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| Authors: | Turinsky AL; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Choufani S; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada., Lu K; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Liu D; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Mashouri P; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Min D; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Weksberg R; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.; Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.; Institute of Medical Science, School of Graduate Studies, University of Toronto, Toronto, Ontario, Canada., Brudno M; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Computer Science, University of Toronto, Toronto, Ontario, Canada.; Techna Institute, University Health Network, Toronto, Ontario, Canada. |
| Source: | Human mutation [Hum Mutat] 2020 Oct; Vol. 41 (10), pp. 1722-1733. Date of Electronic Publication: 2020 Jul 15. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 32623772 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Turinsky+AL%22">Turinsky AL</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Choufani+S%22">Choufani S</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Lu+K%22">Lu K</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Liu+D%22">Liu D</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Mashouri+P%22">Mashouri P</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Min+D%22">Min D</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Weksberg+R%22">Weksberg R</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.; Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.; Institute of Medical Science, School of Graduate Studies, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Brudno+M%22">Brudno M</searchLink>; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Computer Science, University of Toronto, Toronto, Ontario, Canada.; Techna Institute, University Health Network, Toronto, Ontario, Canada. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2020 Oct; Vol. 41 (10), pp. 1722-1733. <i>Date of Electronic Publication: </i>2020 Jul 15. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32623772 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/humu.24076 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1722 Titles: – TitleFull: EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Turinsky AL – PersonEntity: Name: NameFull: Choufani S – PersonEntity: Name: NameFull: Lu K – PersonEntity: Name: NameFull: Liu D – PersonEntity: Name: NameFull: Mashouri P – PersonEntity: Name: NameFull: Min D – PersonEntity: Name: NameFull: Weksberg R – PersonEntity: Name: NameFull: Brudno M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: 2020 Oct Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1098-1004 Numbering: – Type: volume Value: 41 – Type: issue Value: 10 Titles: – TitleFull: Human mutation Type: main |
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