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A cross-package Bioconductor workflow for analysing methylation array data

Methylation in the human genome is known to be associated with development and disease. The Illumina Infinium methylation arrays are by far the most common way to interrogate methylation across the human genome. This paper provides a Bioconductor workflow using multiple packages for the analysis of...

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Detalles Bibliográficos
Autores principales: Maksimovic, Jovana, Phipson, Belinda, Oshlack, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916993/
https://www.ncbi.nlm.nih.gov/pubmed/27347385
http://dx.doi.org/10.12688/f1000research.8839.3
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author Maksimovic, Jovana
Phipson, Belinda
Oshlack, Alicia
author_facet Maksimovic, Jovana
Phipson, Belinda
Oshlack, Alicia
author_sort Maksimovic, Jovana
collection PubMed
description Methylation in the human genome is known to be associated with development and disease. The Illumina Infinium methylation arrays are by far the most common way to interrogate methylation across the human genome. This paper provides a Bioconductor workflow using multiple packages for the analysis of methylation array data. Specifically, we demonstrate the steps involved in a typical differential methylation analysis pipeline including: quality control, filtering, normalization, data exploration and statistical testing for probe-wise differential methylation. We further outline other analyses such as differential methylation of regions, differential variability analysis, estimating cell type composition and gene ontology testing. Finally, we provide some examples of how to visualise methylation array data.
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spelling pubmed-49169932016-06-23 A cross-package Bioconductor workflow for analysing methylation array data Maksimovic, Jovana Phipson, Belinda Oshlack, Alicia F1000Res Method Article Methylation in the human genome is known to be associated with development and disease. The Illumina Infinium methylation arrays are by far the most common way to interrogate methylation across the human genome. This paper provides a Bioconductor workflow using multiple packages for the analysis of methylation array data. Specifically, we demonstrate the steps involved in a typical differential methylation analysis pipeline including: quality control, filtering, normalization, data exploration and statistical testing for probe-wise differential methylation. We further outline other analyses such as differential methylation of regions, differential variability analysis, estimating cell type composition and gene ontology testing. Finally, we provide some examples of how to visualise methylation array data. F1000Research 2017-04-05 /pmc/articles/PMC4916993/ /pubmed/27347385 http://dx.doi.org/10.12688/f1000research.8839.3 Text en Copyright: © 2017 Maksimovic J et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method Article
Maksimovic, Jovana
Phipson, Belinda
Oshlack, Alicia
A cross-package Bioconductor workflow for analysing methylation array data
title A cross-package Bioconductor workflow for analysing methylation array data
title_full A cross-package Bioconductor workflow for analysing methylation array data
title_fullStr A cross-package Bioconductor workflow for analysing methylation array data
title_full_unstemmed A cross-package Bioconductor workflow for analysing methylation array data
title_short A cross-package Bioconductor workflow for analysing methylation array data
title_sort cross-package bioconductor workflow for analysing methylation array data
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916993/
https://www.ncbi.nlm.nih.gov/pubmed/27347385
http://dx.doi.org/10.12688/f1000research.8839.3
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