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