3.8 Article Data Paper

Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip

Journal

GENOMICS DATA
Volume 9, Issue -, Pages 22-24

Publisher

ELSEVIER
DOI: 10.1016/j.gdata.2016.05.012

Keywords

DNA methylation; Infinium MethylationEPIC BeadChip; Cross-hybridising probes; Polymorphic CpG; Quality control

Funding

  1. Mental Health Research UK
  2. Brain & Behavior Research Foundation through a NARSAD Independent Investigator Award
  3. Health Foundation through a Clinician Scientist Fellowship
  4. Brain & Behavior Research Foundation
  5. Wellcome Trust Strategic Support [104036/Z/14/Z]
  6. BBSRC
  7. EPSRC
  8. ESRC
  9. MRC
  10. MRC [G0700704] Funding Source: UKRI
  11. Medical Research Council [G0700704] Funding Source: researchfish

Ask authors/readers for more resources

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. (C) 2016 The Authors. Published by Elsevier Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available