Please use this identifier to cite or link to this item: https://doi.org/10.4161/epi.22102
Title: Measuring the methylome in clinical samples: Improved processing of the infinium human methylation450 beadchip array
Authors: Pan H.
Chen L.
Dogra S.
Teh A.L.
Tan J.H.
Lim Y.I.
Lim Y.C.
Jin S.
Lee Y.K.
Ng P.Y.
Ong M.L.
Barton S.
Chong Y.-S. 
Meaney M.J.
Gluckman P.D.
Stunkel W.
Ding C.
Holbrook J.D.
Keywords: Clinical sample
DNA methylation
EWAS
Genome-wide
InfiniumHD array
RRBS
Issue Date: 2012
Publisher: Taylor and Francis Inc.
Citation: Pan H., Chen L., Dogra S., Teh A.L., Tan J.H., Lim Y.I., Lim Y.C., Jin S., Lee Y.K., Ng P.Y., Ong M.L., Barton S., Chong Y.-S., Meaney M.J., Gluckman P.D., Stunkel W., Ding C., Holbrook J.D. (2012). Measuring the methylome in clinical samples: Improved processing of the infinium human methylation450 beadchip array. Epigenetics 7 (10) : Jan-15. ScholarBank@NUS Repository. https://doi.org/10.4161/epi.22102
Abstract: The Infinium Human Methylation450 BeadChip ArrayTM (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. © 2012 Landes Bioscience.
Source Title: Epigenetics
URI: https://scholarbank.nus.edu.sg/handle/10635/185702
ISSN: 15592294
DOI: 10.4161/epi.22102
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