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Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array
The Infinium Human Methylation450 BeadChip Array(TM) (Infinium 450K) is an important tool for studying epigenetic patterns associated with disease. This array offers a high-throughput, low cost alternative to more comprehensive sequencing-based methodologies. Here we compare data generated by interr...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469459/ https://www.ncbi.nlm.nih.gov/pubmed/22964528 http://dx.doi.org/10.4161/epi.22102 |
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author | Pan, Hong Chen, Li Dogra, Shaillay Ling Teh, Ai Tan, Jun Hao Lim, Yubin I. Lim, Yen Ching Jin, Shengnan Lee, Yew Kok Ng, Poh Yong Ong, Mei Lyn Barton, Shelia Chong, Yap-Seng Meaney, Michael J. Gluckman, Peter D. Stunkel, Walter Ding, Chunming Holbrook, Joanna D. |
author_facet | Pan, Hong Chen, Li Dogra, Shaillay Ling Teh, Ai Tan, Jun Hao Lim, Yubin I. Lim, Yen Ching Jin, Shengnan Lee, Yew Kok Ng, Poh Yong Ong, Mei Lyn Barton, Shelia Chong, Yap-Seng Meaney, Michael J. Gluckman, Peter D. Stunkel, Walter Ding, Chunming Holbrook, Joanna D. |
author_sort | Pan, Hong |
collection | PubMed |
description | The Infinium Human Methylation450 BeadChip Array(TM) (Infinium 450K) is an important tool for studying epigenetic patterns associated with disease. This array offers a high-throughput, low cost alternative to more comprehensive sequencing-based methodologies. Here we compare data generated by interrogation of the same seven clinical samples by Infinium 450K and reduced representation bisulfite sequencing (RRBS). This is the largest data set comparing Infinium 450K array to the comprehensive RRBS methodology reported so far. We show good agreement between the two methodologies. A read depth of four or more reads in the RRBS data was sufficient to achieve good agreement with Infinium 450K. However, we observe that intermediate methylation values (20–80%) are more variable between technologies than values at the extremes of the bimodal methylation distribution. We describe careful processing of Infinium 450K data to correct for known limitations and batch effects. Using methodologies proposed by others and newly implemented and combined in this report, agreement of Infinium 450K data with independent techniques can be vastly improved. |
format | Online Article Text |
id | pubmed-3469459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-34694592012-10-23 Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array Pan, Hong Chen, Li Dogra, Shaillay Ling Teh, Ai Tan, Jun Hao Lim, Yubin I. Lim, Yen Ching Jin, Shengnan Lee, Yew Kok Ng, Poh Yong Ong, Mei Lyn Barton, Shelia Chong, Yap-Seng Meaney, Michael J. Gluckman, Peter D. Stunkel, Walter Ding, Chunming Holbrook, Joanna D. Epigenetics Research Paper The Infinium Human Methylation450 BeadChip Array(TM) (Infinium 450K) is an important tool for studying epigenetic patterns associated with disease. This array offers a high-throughput, low cost alternative to more comprehensive sequencing-based methodologies. Here we compare data generated by interrogation of the same seven clinical samples by Infinium 450K and reduced representation bisulfite sequencing (RRBS). This is the largest data set comparing Infinium 450K array to the comprehensive RRBS methodology reported so far. We show good agreement between the two methodologies. A read depth of four or more reads in the RRBS data was sufficient to achieve good agreement with Infinium 450K. However, we observe that intermediate methylation values (20–80%) are more variable between technologies than values at the extremes of the bimodal methylation distribution. We describe careful processing of Infinium 450K data to correct for known limitations and batch effects. Using methodologies proposed by others and newly implemented and combined in this report, agreement of Infinium 450K data with independent techniques can be vastly improved. Landes Bioscience 2012-10-01 /pmc/articles/PMC3469459/ /pubmed/22964528 http://dx.doi.org/10.4161/epi.22102 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Research Paper Pan, Hong Chen, Li Dogra, Shaillay Ling Teh, Ai Tan, Jun Hao Lim, Yubin I. Lim, Yen Ching Jin, Shengnan Lee, Yew Kok Ng, Poh Yong Ong, Mei Lyn Barton, Shelia Chong, Yap-Seng Meaney, Michael J. Gluckman, Peter D. Stunkel, Walter Ding, Chunming Holbrook, Joanna D. Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title | Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title_full | Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title_fullStr | Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title_full_unstemmed | Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title_short | Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array |
title_sort | measuring the methylome in clinical samples: improved processing of the infinium human methylation450 beadchip array |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469459/ https://www.ncbi.nlm.nih.gov/pubmed/22964528 http://dx.doi.org/10.4161/epi.22102 |
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