minfi
minfi performs analysis and visualization of Illumina Infinium DNA methylation array data for HumanMethylation450 ('450k') and HumanMethylationEPIC ('EPIC') arrays to support integration and normalization across these platforms.
Key Features:
- Platform Support: Supports analysis of Illumina Infinium HumanMethylation450 ('450k') and HumanMethylationEPIC ('EPIC') array data within a unified framework.
- Visualization: Provides visualization capabilities for DNA methylation data derived from Infinium arrays.
- Normalization Methods: Implements the single-sample Noob (ssNoob) normalization method for processing individual arrays.
- Preprocessing: Enables incremental preprocessing of individual methylation arrays using ssNoob to maintain consistency across samples.
- Joint Analysis and Normalization: Facilitates joint analysis and normalization of 450k and EPIC platform data for comparative studies.
Scientific Applications:
- Data Integration: Integrates datasets from different generations of Illumina methylation arrays to support longitudinal and large-scale epigenetic studies.
- Comparative Studies and Meta-analysis: Enables comparative analyses and meta-analyses across 450k and EPIC datasets through joint normalization.
- Cell Type Composition Estimation: Estimates cell type composition in samples using reference 450k datasets to account for cellular heterogeneity in methylation analyses.
Methodology:
Uses preprocessing, normalization, and analysis of Illumina Infinium methylation data including the single-sample Noob (ssNoob) method and procedures for joint normalization of 450k and EPIC arrays.
Topics
Collections
Details
- License:
- Artistic-2.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 1/17/2017
- Last Updated:
- 1/13/2019
Operations
Publications
Fortin J, Triche TJ, Hansen KD. Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi. Bioinformatics. 2016;33(4):558-560. doi:10.1093/bioinformatics/btw691. PMID:28035024. PMCID:PMC5408810.