methylCC

methylCC estimates cell-type composition from whole blood DNA methylation (DNAm) data in a technology-independent manner to account for intra-sample cellular heterogeneity.


Key Features:

  • Technology independence: Provides cell composition estimation that is applicable across multiple DNAm measurement platforms including Illumina 450K microarray, whole genome bisulfite sequencing (WGBS), and reduced representation bisulfite sequencing (RRBS).
  • Whole blood focus: Targets estimation of proportions of constituent cell types within whole blood DNAm samples.
  • Mitigation of platform-specific bias: Produces consistent cell composition estimates across technologies to reduce technology-specific biases in downstream analyses.
  • Implementation: Distributed as an R/Bioconductor package for integration into R-based analysis workflows.
  • Control of cellular heterogeneity: Explicitly addresses intra-sample cellular heterogeneity that can confound DNAm association studies.

Scientific Applications:

  • Cell composition deconvolution: Estimating proportions of blood cell types from DNAm data for studies using whole blood samples.
  • Confounding adjustment in epigenetic association studies: Adjusting for cellular heterogeneity to reduce false positives and confounding in DNAm-outcome associations.
  • Cross-technology comparisons: Enabling consistent cell composition estimates for comparative analyses across Illumina 450K, WGBS, and RRBS datasets.

Methodology:

Implemented as an R/Bioconductor package that performs technology-independent estimation of cell type composition from whole blood DNAm data applicable to Illumina 450K microarray, WGBS, and RRBS.

Topics

Details

License:
CC-BY-4.0
Tool Type:
command-line tool
Programming Languages:
R
Added:
1/14/2020
Last Updated:
12/28/2020

Operations

Publications

Hicks SC, Irizarry RA. methylCC: technology-independent estimation of cell type composition using differentially methylated regions. Genome Biology. 2019;20(1). doi:10.1186/s13059-019-1827-8. PMID:31783894. PMCID:PMC6883691.

PMID: 31783894
PMCID: PMC6883691
Funding: - National Institute of General Medical Sciences: GM083084, GM103552 - National Human Genome Research Institute: HG005220

Links