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 J1ORCID,Zwamborn Ramona A J1,Hannon Eilis J2ORCID,Dekker Annelot M1,van Eijk Kristel R1,Walker Emma M2,Iacoangeli Alfredo34ORCID,Jones Ashley R3,Shatunov Aleksey3,Khleifat Ahmad Al3,Opie-Martin Sarah3,Shaw Christopher E35,Morrison Karen E6,Shaw Pamela J7,McLaughlin Russell L8ORCID,Hardiman Orla910,Al-Chalabi Ammar311,Van Den Berg Leonard H1,Mill Jonathan2,Veldink Jan H1

Affiliation:

1. Department of Neurology, UMC Utrecht Brain Center, 3584 CG, Utrecht, the Netherlands

2. University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK

3. Department of Basic and Clinical Neuroscience, King’s College London, Maurice Wohl Clinical Neuroscience Institute, London SE5 9RS, UK

4. Department of Biostatistics and Health Informatics, King’s College London, London SE5 8AF, UK

5. UK Dementia Research Institute, King’s College London, London WC2R 2LS, UK

6. Faculty of Medicine, Health & Life Sciences, Queen’s University Belfast, 90 Lisburn Road, Belfast, BT9 6AG, Northern Ireland, UK

7. Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK

8. Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin D02 DK07, Republic of Ireland

9. Academic Unit of Neurology, Trinity College Dublin, Trinity Biomedical Sciences Institute, Dublin D02 PN40, Republic of Ireland

10. Department of Neurology, Beaumont Hospital, Dublin D02 PN40, Republic of Ireland

11. Department of Neurology, King’s College Hospital, Bessemer Road, London, SE5 9RX, UK

Abstract

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.

Funder

ALS Foundation Netherlands

MND Association

European Research Council

Health Holland, Top Sector Life Sciences & Health

EU Joint Programme - Neurodegenerative Disease Research

Medical Research Council

Motor Neurone Disease Association

National Institute for Health Research

Maudsley Biomedical Research Centre

UK National DNA Bank for MND Research

Wellcome Trust

Dementia Biomedical Research Unit and Biomedical Research Centre in Mental Health

South London and Maudsley NHS Foundation Trust

King’s College London

Science Foundation Ireland

Medical Research Council Clinical Infrastructure Award

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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