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funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types.
Oros Klein, Kathleen; Grinek, Stepan; Bernatsky, Sasha; Bouchard, Luigi; Ciampi, Antonio; Colmegna, Ines; Fortin, Jean-Philippe; Gao, Long; Hivert, Marie-France; Hudson, Marie; Kobor, Michael S; Labbe, Aurelie; MacIsaac, Julia L; Meaney, Michael J; Morin, Alexander M; O'Donnell, Kieran J; Pastinen, Tomi; Van Ijzendoorn, Marinus H; Voisin, Gregory; Greenwood, Celia M T.
Afiliação
  • Oros Klein K; Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada, Ludmer Center for Neuroinformatics and Mental Health.
  • Grinek S; Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada, Ludmer Center for Neuroinformatics and Mental Health.
  • Bernatsky S; Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, McGill University, Montreal, QC H4A 3J1, Canada.
  • Bouchard L; ECOGENE-21, Centre intégré universitaire de santé et de service sociaux du Saguenay-Lac-Saint-Jean, QC G8H 3P7, Canada, Department of Biochemistry, Université de Sherbrooke, QC J1K 2R1, Canada.
  • Ciampi A; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC H3A 1A2, Canada.
  • Colmegna I; Division of Experimental Medicine, McGill University Health Centre, McGill University, Montreal, QC H3A 1A3, Canada.
  • Fortin JP; Department of Biostatistics, Johns Hopkins University, Baltimore, MD 21218, USA.
  • Gao L; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC H3A 1A2, Canada.
  • Hivert MF; Department of Population Medicine, Harvard Medical School, Harvard Pilgrim Health Care Institute, Boston, MA 02215, USA, Department of Medicine, Division of Endocrinology, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
  • Hudson M; Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada, Department of Medicine, McGill University Health Center, Montreal, QC H4A 3J1, Canada.
  • Kobor MS; Canadian Institute for Advanced Research, Child, and Brain Development Program, Toronto, ON M5G 1Z8, Canada, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC V5Z 4H4, Canada, Department of Medical Genetics, University of British Columbia, Vancouver,
  • Labbe A; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC H3A 1A2, Canada.
  • MacIsaac JL; Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC V5Z 4H4, Canada, Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada.
  • Meaney MJ; Ludmer Center for Neuroinformatics and Mental Health, Canadian Institute for Advanced Research, Child, and Brain Development Program, Toronto, ON M5G 1Z8, Canada, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC V5Z 4H4, Canada, Douglas Mental Health
  • Morin AM; Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC V5Z 4H4, Canada, Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada.
  • O'Donnell KJ; Douglas Mental Health University Institute, McGill University, Montreal, QC H4H 1R3, Canada.
  • Pastinen T; Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada and.
  • Van Ijzendoorn MH; Centre for Child and Family Studies, Leiden University, Leiden 2300 RB, The Netherlands.
  • Voisin G; Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada, Ludmer Center for Neuroinformatics and Mental Health.
  • Greenwood CM; Lady Davis Institute, Jewish General Hospital, Montreal, QC H3T 1E2, Canada, Department of Biochemistry, Université de Sherbrooke, QC J1K 2R1, Canada, Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC H3A 1A2, Canada, Department of Human Genetics, McG
Bioinformatics ; 32(4): 593-5, 2016 Feb 15.
Article em En | MEDLINE | ID: mdl-26500152
ABSTRACT
MOTIVATION DNA methylation patterns are well known to vary substantially across cell types or tissues. Hence, existing normalization methods may not be optimal if they do not take this into account. We therefore present a new R package for normalization of data from the Illumina Infinium Human Methylation450 BeadChip (Illumina 450 K) built on the concepts in the recently published funNorm method, and introducing cell-type or tissue-type flexibility.

RESULTS:

funtooNorm is relevant for data sets containing samples from two or more cell or tissue types. A visual display of cross-validated errors informs the choice of the optimal number of components in the normalization. Benefits of cell (tissue)-specific normalization are demonstrated in three data sets. Improvement can be substantial; it is strikingly better on chromosome X, where methylation patterns have unique inter-tissue variability. AVAILABILITY AND IMPLEMENTATION An R package is available at https//github.com/GreenwoodLab/funtooNorm, and has been submitted to Bioconductor at http//bioconductor.org.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Especificidade de Órgãos / Doenças Autoimunes / Software / Diabetes Gestacional / Linhagem da Célula / Metilação de DNA Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Especificidade de Órgãos / Doenças Autoimunes / Software / Diabetes Gestacional / Linhagem da Célula / Metilação de DNA Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2016 Tipo de documento: Article