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.

PMID: 28035024
PMCID: PMC5408810
Funding: - National Cancer Institute: U24CA180996

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