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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
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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. |
format | Online Article Text |
id | pubmed-4916993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
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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