Home LiteratureArticle Details
PMID: 22171553 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

Batch effect correction for genome-wide methylation data with Illumina Infinium platform.

BMC medical genomics ·Vol. 4 ·2011-12-16 ·Pages 84

Sun Z, Chai HS, Wu Y, White WM, Donkena KV, Klein CJ, Garovic VD, Therneau TM, Kocher JP

Abstract

Genome-wide methylation profiling has led to more comprehensive insights into gene regulation mechanisms and potential therapeutic targets. Illumina Human Methylation BeadChip is one of the most commonly used genome-wide methylation platforms. Similar to other microarray experiments, methylation data is susceptible to various technical artifacts, particularly batch effects. To date, little attention has been given to issues related to normalization and batch effect correction for this kind of data. We evaluated three common normalization approaches and investigated their performance in batch effect removal using three datasets with different degrees of batch effects generated from HumanMethylation27 platform: quantile normalization at average β value (QNβ); two step quantile normalization at probe signals implemented in "lumi" package of R (lumi); and quantile normalization of A and B signal separately (ABnorm). Subsequent Empirical Bayes (EB) batch adjustment was also evaluated. Each normalization could remove a portion of batch effects and their effectiveness differed depending on the severity of batch effects in a dataset. For the dataset with minor batch effects (Dataset 1), normalization alone appeared adequate and "lumi" showed the best performance. However, all methods left substantial batch effects intact in the datasets with obvious batch effects and further correction was necessary. Without any correction, 50 and 66 percent of CpGs were associated with batch effects in Dataset 2 and 3, respectively. After QNβ, lumi or ABnorm, the number of CpGs associated with batch effects were reduced to 24, 32, and 26 percent for Dataset 2; and 37, 46, and 35 percent for Dataset 3, respectively. Additional EB correction effectively removed such remaining non-biological effects. More importantly, the two-step procedure almost tripled the numbers of CpGs associated with the outcome of interest for the two datasets. Genome-wide methylation data from Infinium Methylation BeadChip can be susceptible to batch effects with profound impacts on downstream analyses and conclusions. Normalization can reduce part but not all batch effects. EB correction along with normalization is recommended for effective batch effect removal.

MeSH Terms
Adult CpG Islands/genetics DNA Methylation/genetics Databases, Genetic Genome, Human/genetics Humans Male Oligonucleotide Array Sequence Analysis/methods Reproducibility of Results
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Sun Zhifu
Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, 200 First Street, Rochester, MN 55905, USA.
Chai High Seng
Wu Yanhong
White Wendy M
Donkena Krishna V
Klein Christopher J
Garovic Vesna D
Therneau Terry M
Kocher Jean-Pierre A
References (32)
32 references, click to expand
  1. Principles and challenges of genomewide DNA methylation analysis.
    Nat Rev Genet. 2010 Mar;11(3):191-203 PMID: 20125086
  2. Aberrant global methylation patterns affect the molecular pathogenesis and prognosis of multiple myeloma.
    Blood. 2011 Jan 13;117(2):553-62 PMID: 20944071
  3. Adjustment of systematic microarray data biases.
    Bioinformatics. 2004 Jan 1;20(1):105-14 PMID: 14693816
  4. Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2.
    Nature. 2010 Dec 9;468(7325):839-43 PMID: 21057493
  5. The removal of multiplicative, systematic bias allows integration of breast cancer gene expression datasets - improving meta-analysis and prediction of prognosis.
    BMC Med Genomics. 2008 Sep 21;1:42 PMID: 18803878
  6. Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
    BMC Bioinformatics. 2008 Oct 02;9:409 PMID: 18831757
  7. Tackling the widespread and critical impact of batch effects in high-throughput data.
    Nat Rev Genet. 2010 Oct;11(10):733-9 PMID: 20838408
  8. Preprocessing differential methylation hybridization microarray data.
    BioData Min. 2011 May 16;4:13 PMID: 21575229
  9. Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.
    Genome Res. 2010 Apr;20(4):440-6 PMID: 20219944
  10. Promoter hypermethylation in prostate cancer.
    Cancer Control. 2010 Oct;17(4):245-55 PMID: 20861812
  11. Absolute quantitation of DNA methylation of 28 candidate genes in prostate cancer using pyrosequencing.
    Dis Markers. 2011;30(4):151-61 PMID: 21694441
  12. Human housekeeping genes are compact.
    Trends Genet. 2003 Jul;19(7):362-5 PMID: 12850439
  13. Obesity related methylation changes in DNA of peripheral blood leukocytes.
    BMC Med. 2010 Dec 21;8:87 PMID: 21176133
  14. Genome-wide DNA methylation analysis for diabetic nephropathy in type 1 diabetes mellitus.
    BMC Med Genomics. 2010 Aug 05;3:33 PMID: 20687937
  15. Genome-wide DNA methylation profiling using Infinium® assay.
    Epigenomics. 2009 Oct;1(1):177-200 PMID: 22122642
  16. Adjusting batch effects in microarray expression data using empirical Bayes methods.
    Biostatistics. 2007 Jan;8(1):118-27 PMID: 16632515
  17. Altered DNA methylation in leukocytes with trisomy 21.
    PLoS Genet. 2010 Nov 18;6(11):e1001212 PMID: 21124956
  18. Supervised normalization of microarrays.
    Bioinformatics. 2010 May 15;26(10):1308-15 PMID: 20363728
  19. DNA methylation in glioblastoma: impact on gene expression and clinical outcome.
    BMC Genomics. 2010 Dec 14;11:701 PMID: 21156036
  20. Removing batch effects in analysis of expression microarray data: an evaluation of six batch adjustment methods.
    PLoS One. 2011 Feb 28;6(2):e17238 PMID: 21386892
  21. DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines.
    Genome Biol. 2011;12(1):R10 PMID: 21251332
  22. The power and the promise of DNA methylation markers.
    Nat Rev Cancer. 2003 Apr;3(4):253-66 PMID: 12671664
  23. Singular value decomposition for genome-wide expression data processing and modeling.
    Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10101-6 PMID: 10963673
  24. Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.
    Genome Res. 2010 Apr;20(4):434-9 PMID: 20219945
  25. An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer.
    BMC Syst Biol. 2010 May 17;4:67 PMID: 20478067
  26. Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns.
    Hum Mol Genet. 2009 Dec 15;18(24):4808-17 PMID: 19776032
  27. DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer.
    Genome Res. 2011 Jul;21(7):1017-27 PMID: 21521786
  28. Capturing heterogeneity in gene expression studies by surrogate variable analysis.
    PLoS Genet. 2007 Sep;3(9):1724-35 PMID: 17907809
  29. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias.
    Bioinformatics. 2003 Jan 22;19(2):185-93 PMID: 12538238
  30. A comparison of batch effect removal methods for enhancement of prediction performance using MAQC-II microarray gene expression data.
    Pharmacogenomics J. 2010 Aug;10(4):278-91 PMID: 20676067
  31. Genome-wide DNA methylation analysis in cohesin mutant human cell lines.
    Nucleic Acids Res. 2010 Sep;38(17):5657-71 PMID: 20448023
  32. lumi: a pipeline for processing Illumina microarray.
    Bioinformatics. 2008 Jul 1;24(13):1547-8 PMID: 18467348
Article Info
Journal
BMC medical genomics
Abbr.
BMC Med Genomics
ISSN
1755-8794
Published
2011-12-16
Epub
2011-00-16
Pages
84
Language
English
Region
England
NLM ID
101319628
PMCID
PMC3265417
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com