The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Review of processing and analysis methods for DNA methylation array data
Open accessAbstract
The promise of epigenome-wide association studies and cancer-specific somatic DNA methylation changes in improving our understanding of cancer, coupled with the decreasing cost and increasing coverage of DNA methylation microarrays, has brought about a surge in the use of these technologies. Here, we aim to provide both a review of issues encountered in the processing and analysis of array-based DNA methylation data and a summary of the advantages of recent approaches proposed for handling those issues, focusing on approaches publicly available in open-source environments such as R and Bioconductor. We hope that the processing tools and analysis flowchart described herein will facilitate researchers to effectively use these powerful DNA methylation array-based platforms, thereby advancing our understanding of human health and disease.
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Cites
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
Edgar, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.207 · Cited by 13,288
A simulation study of the number of events per variable in logistic regression analysis
Peduzzi, P., Concato, J., Kemper, E., Holford, T. R., & Feinstein, A. R. (1996) · Journal of Clinical Epidemiology · doi:10.1016/s0895-4356(96)00236-3 · Cited by 9,655
Adjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
Barretina, J., Caponigro, G., Stransky, N., Venkatesan, K., Margolin, A. A., Kim, S., Wilson, C. J., Lehár, J., Kryukov, G. V., Sonkin, D., et al. (2012) · Nature · doi:10.1038/nature11003 · Cited by 7,950
Why Most Published Research Findings Are False
Ioannidis, J. P. A. (2005) · CHANCE · doi:10.1080/09332480.2005.10722754 · Cited by 4,702 · cited 2×
“We also aim to counter some of the perceived limitations of these arrays, i.e., that there are too many “false positives” in analyzing micro-array data (Ioannidis, 2007).”
BackgroundGenome-wide methylation profiles reveal quantitative views of human aging rates
Hannum, G., Guinney, J., Zhao, L., Zhang, L., Hughes, G., Sadda, S., Klotzle, B., Bibikova, M., Fan, J.-B., Gao, Y., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2012.10.016 · Cited by 4,270
DNA methylation arrays as surrogate measures of cell mixture distribution
Houseman, E. A., Accomando, W. P., Koestler, D. C., Christensen, B. C., Marsit, C. J., Nelson, H. H., Wiencke, J. K., & Kelsey, K. T. (2012) · BMC Bioinformatics · doi:10.1186/1471-2105-13-86 · Cited by 3,175
Self-citationIntegrating common and rare genetic variation in diverse human populations
The International HapMap 3 Consortium (2010) · Nature · doi:10.1038/nature09298 · Cited by 3,026
A decade of exploring the cancer epigenome—biological and translational implications
Baylin, S. B., & Jones, P. A. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3130 · Cited by 2,871
Tackling the widespread and critical impact of batch effects in high-throughput data
Leek, J. T., Scharpf, R. B., Bravo, H. C., Simcha, D., Langmead, B., Johnson, W. E., Geman, D., Baggerly, K., & Irizarry, R. A. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2825 · Cited by 2,196
Cited by
Influence of environmental exposure on human epigenetic regulation
Marsit, C. J. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.106971 · Cited by 253
Self-citationMcEwen, L. M., Jones, M. J., Lin, D. T. S., Edgar, R. D., Husquin, L. T., MacIsaac, J. L., Ramadori, K. E., Morin, A. M., Rider, C. F., Carlsten, C., et al. (2018) · Clinical Epigenetics · doi:10.1186/s13148-018-0556-2 · Cited by 147
Liu, Y., Eliot, M. N., Papandonatos, G. D., Kelsey, K. T., Fore, R., Langevin, S., Buckley, J., Chen, A., Lanphear, B. P., Cecil, K. M., et al. (2022) · Environmental Health Perspectives · doi:10.1289/ehp10118 · Cited by 78
Self-citationDeepMF: deciphering the latent patterns in omics profiles with a deep learning method
Chen, L., Xu, J., & Li, S. C. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-3291-6 · Cited by 23
“…S j , where u i and v j are vectors of size K which encode structures that underlie the data; that is, the predicted element of feature F i on sample S j is calculated as: The predicted matrix ˆ A can be thought of as the product of the feature latent factor matrix U and sample latent factor matrix”
BackgroundKoenig, M. J., Agana, B. A., Kaufman, J. M., Sharpnack, M. F., Wang, W. Z., Weigel, C., Navarro, F. C. P., Amann, J. M., Cacciato, N., Arasada, R. R., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-3199 · Cited by 18
Metadata
- Authors
- Wilhelm-Benartzi, C. S., Koestler, D. C., Karagas, M. R., Flanagan, J. M., Christensen, B. C., Kelsey, K. T., Marsit, C. J., Houseman, E. A., & Brown, R.
- Venue
- British Journal of Cancer
- Published
- 2013-08-27
- Volume
- 109
- Issue
- 6
- Pages
- 1394-1402
- ISSN
- 0007-0920 (ISSN-L)
- 1532-1827
- OpenAlex
- W2085245717
- Cited by
- 201
- References
- 18
- FWCI
- 6.72
- Type
- journal article
- Language
- en
- Open access
- hybrid
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