Open access · CC-BY
via OpenAlex
DNA methylation arrays as surrogate measures of cell mixture distribution
Eugene Andres Houseman, William P. Accomando, Devin C. Koestler, Brock C. Christensen, Carmen J. Marsit, Heather H. Nelson, John K. Wiencke, Karl T. Kelsey
BMC Bioinformatics · 2012 · ▲ 3,513 citations
Abstract
BACKGROUND: There has been a long-standing need in biomedical research for a method that quantifies the normally mixed composition of leukocytes beyond what is possible by simple histological or flow cytometric assessments. The latter is restricted by the labile nature of protein epitopes, requirements for cell processing, and timely cell analysis. In a diverse array of diseases and following numerous immune-toxic exposures, leukocyte composition will critically inform the underlying immuno-biology to most chronic medical conditions. Emerging research demonstrates that DNA methylation is responsible for cellular differentiation, and when measured in whole peripheral blood, serves to distinguish cancer cases from controls. RESULTS: Here we present a method, similar to regression calibration, for inferring changes in the distribution of white blood cells between different subpopulations (e.g. cases and controls) using DNA methylation signatures, in combination with a previously obtained external validation set consisting of signatures from purified leukocyte samples. We validate the fundamental idea in a cell mixture reconstruction experiment, then demonstrate our method on DNA methylation data sets from several studies, including data from a Head and Neck Squamous Cell Carcinoma (HNSCC) study and an ovarian cancer study. Our method produces results consistent with prior biological findings, thereby validating the approach. CONCLUSIONS: Our method, in combination with an appropriate external validation set, promises new opportunities for large-scale immunological studies of both disease states and noxious exposures.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.1186/1471-2105-13-86
- Canonical
- link ↗
- Fetched
- 2026-10-02 MST
Cite this
APA
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). DNA methylation arrays as surrogate measures of cell mixture distribution. <em>BMC Bioinformatics</em>. https://doi.org/10.1186/1471-2105-13-86
Vancouver
Houseman EA, Accomando WP, Koestler DC, Christensen BC, Marsit CJ, Nelson HH, et al. DNA methylation arrays as surrogate measures of cell mixture distribution. BMC Bioinformatics. 2012. doi:10.1186/1471-2105-13-86.
BibTeX
@article{eugene2012DNAmet,
title = {DNA methylation arrays as surrogate measures of cell mixture distribution},
author = {Eugene Andres Houseman and William P. Accomando and Devin C. Koestler and Brock C. Christensen and Carmen J. Marsit and Heather H. Nelson and John K. Wiencke and Karl T. Kelsey},
journal = {BMC Bioinformatics},
year = {2012},
doi = {10.1186/1471-2105-13-86},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
Spiral (Imperial College London) 2010
Preprint · CC-BY
Defining the clinical role of the mammalian target of rapamycin (mTOR) in lung cancer
The British Journal of Psychiatry 2026
Citation only
Recalibrating the epigenetic clock reveals divergent DNA methylation age signatures across schizophrenia, bipolar disorder and major depressive disorder
Epigenetics & Chromatin 2015
Open access · CC-BY
Concordant and discordant DNA methylation signatures of aging in human blood and brain
PLoS ONE 2009
Open access · CC-BY
An Epigenetic Signature in Peripheral Blood Predicts Active Ovarian Cancer
BMC Bioinformatics 2008
Open access · CC-BY
Model-based clustering of DNA methylation array data: a recursive-partitioning algorithm for high-dimensional data arising as a mixture of beta distributions
biorxiv 2024
Preprint · CC-BY