Abstract

Illumina DNA methylation arrays are a widely used tool for performing genome-wide DNA methylation analyses. However, measurements obtained from these arrays may be affected by technical artefacts that result in spurious associations if left unchecked. Cross-reactivity represents one of the major challenges, meaning that probes may map to multiple regions in the genome. Although several studies have reported on this issue, few studies have empirically examined the impact of cross-reactivity in an epigenome-wide association study (EWAS). In this paper, we report on cross-reactivity issues that we discovered in a large EWAS on the presence of the C9orf72 repeat expansion in ALS patients. Specifically, we found that that the majority of the significant probes inadvertently cross-hybridized to the C9orf72 locus. Importantly, these probes were not flagged as cross-reactive in previous studies, leading to novel insights into the extent to which cross-reactivity can impact EWAS. Our findings are particularly relevant for epigenetic studies into diseases associated with repeat expansions and other types of structural variation. More generally however, considering that most spurious associations were not excluded based on pre-defined sets of cross-reactive probes, we believe that the presented data-driven flag and consider approach is relevant for any type of EWAS.

Details

Title
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies
Author
Hop, Paul J 1   VIAFID ORCID Logo  ; Zwamborn, Ramona A J 1 ; Hannon, Eilis J 2   VIAFID ORCID Logo  ; Dekker, Annelot M 1 ; van Eijk, Kristel R 1 ; Walker, Emma M 2 ; Iacoangeli, Alfredo 3   VIAFID ORCID Logo  ; Jones, Ashley R 3 ; Shatunov, Aleksey 3 ; Ahmad Al Khleifat 3 ; Opie-Martin, Sarah 3 ; Shaw, Christopher E 3 ; Morrison, Karen E 4 ; Shaw, Pamela J 5 ; McLaughlin, Russell L 6   VIAFID ORCID Logo  ; Hardiman, Orla 7 ; Al-Chalabi, Ammar 3 ; Leonard H Van Den Berg 1 ; Mill, Jonathan 2 ; Veldink, Jan H 1 

 Department of Neurology , UMC Utrecht Brain Center, 3584 CG, Utrecht, the Netherlands 
 University of Exeter Medical School, University of Exeter , Exeter EX2 5DW, UK 
 Department of Basic and Clinical Neuroscience , King’s College London, Maurice Wohl Clinical Neuroscience Institute, London SE5 9RS, UK 
 Faculty of Medicine, Health & Life Sciences, Queen’s University Belfast , 90 Lisburn Road, Belfast, BT9 6AG, Northern Ireland, UK 
 Sheffield Institute for Translational Neuroscience, University of Sheffield , Sheffield S10 2HQ, UK 
 Complex Trait Genomics Laboratory, Smurfit Institute of Genetics , Trinity College Dublin, Dublin D02 DK07, Republic of Ireland 
 Academic Unit of Neurology, Trinity College Dublin , Trinity Biomedical Sciences Institute, Dublin D02 PN40, Republic of Ireland 
Publication year
2020
Publication date
Dec 2020
Publisher
Oxford University Press
e-ISSN
26319268
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3170917170
Copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.