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Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip
Genome-wide analysis of DNA methylation has now become a relatively inexpensive technique thanks to array-based methylation profiling technologies. The recently developed Illumina Infinium MethylationEPIC BeadChip interrogates methylation at over 850,000 sites across the human genome, covering 99% o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909830/ https://www.ncbi.nlm.nih.gov/pubmed/27330998 http://dx.doi.org/10.1016/j.gdata.2016.05.012 |
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author | McCartney, Daniel L. Walker, Rosie M. Morris, Stewart W. McIntosh, Andrew M. Porteous, David J. Evans, Kathryn L. |
author_facet | McCartney, Daniel L. Walker, Rosie M. Morris, Stewart W. McIntosh, Andrew M. Porteous, David J. Evans, Kathryn L. |
author_sort | McCartney, Daniel L. |
collection | PubMed |
description | Genome-wide analysis of DNA methylation has now become a relatively inexpensive technique thanks to array-based methylation profiling technologies. The recently developed Illumina Infinium MethylationEPIC BeadChip interrogates methylation at over 850,000 sites across the human genome, covering 99% of RefSeq genes. This array supersedes the widely used Infinium HumanMethylation450 BeadChip, which has permitted insights into the relationship between DNA methylation and a wide range of conditions and traits. Previous research has identified issues with certain probes on both the HumanMethylation450 BeadChip and its predecessor, the Infinium HumanMethylation27 BeadChip, which were predicted to affect array performance. These issues concerned probe-binding specificity and the presence of polymorphisms at target sites. Using in silico methods, we have identified probes on the Infinium MethylationEPIC BeadChip that are predicted to (i) measure methylation at polymorphic sites and (ii) hybridise to multiple genomic regions. We intend these resources to be used for quality control procedures when analysing data derived from this platform. |
format | Online Article Text |
id | pubmed-4909830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49098302016-06-21 Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip McCartney, Daniel L. Walker, Rosie M. Morris, Stewart W. McIntosh, Andrew M. Porteous, David J. Evans, Kathryn L. Genom Data Data in Brief Genome-wide analysis of DNA methylation has now become a relatively inexpensive technique thanks to array-based methylation profiling technologies. The recently developed Illumina Infinium MethylationEPIC BeadChip interrogates methylation at over 850,000 sites across the human genome, covering 99% of RefSeq genes. This array supersedes the widely used Infinium HumanMethylation450 BeadChip, which has permitted insights into the relationship between DNA methylation and a wide range of conditions and traits. Previous research has identified issues with certain probes on both the HumanMethylation450 BeadChip and its predecessor, the Infinium HumanMethylation27 BeadChip, which were predicted to affect array performance. These issues concerned probe-binding specificity and the presence of polymorphisms at target sites. Using in silico methods, we have identified probes on the Infinium MethylationEPIC BeadChip that are predicted to (i) measure methylation at polymorphic sites and (ii) hybridise to multiple genomic regions. We intend these resources to be used for quality control procedures when analysing data derived from this platform. Elsevier 2016-05-26 /pmc/articles/PMC4909830/ /pubmed/27330998 http://dx.doi.org/10.1016/j.gdata.2016.05.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Data in Brief McCartney, Daniel L. Walker, Rosie M. Morris, Stewart W. McIntosh, Andrew M. Porteous, David J. Evans, Kathryn L. Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title | Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title_full | Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title_fullStr | Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title_full_unstemmed | Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title_short | Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip |
title_sort | identification of polymorphic and off-target probe binding sites on the illumina infinium methylationepic beadchip |
topic | Data in Brief |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909830/ https://www.ncbi.nlm.nih.gov/pubmed/27330998 http://dx.doi.org/10.1016/j.gdata.2016.05.012 |
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