MEA

MEA performs genome-wide allele-specific analysis of DNA methylation (DNAme) and histone modifications to map allelic epigenetic regulation at SNV- and INDEL-resolved loci.


Key Features:

  • Allele-Specific Analysis: Incorporates single nucleotide variants (SNVs) and insertions/deletions (INDELs) to analyze allele-specific transcriptional regulation and epigenetic marks.
  • INDEL-aware Low Reference Bias: Uses INDEL-aware algorithms to reduce systematic reference bias and improve allelic mapping of DNA methylation.
  • Integration of Epigenomic Datasets: Integrates DNAme with RNA-seq and ChIP-seq data to relate transcriptional activity to epigenetic modifications.
  • Allele-specific Detection of Histone Marks: Detects allele-specific enrichment of histone modifications including H3K27ac alongside DNAme at imprinted and monoallelically expressed genes.
  • Standardized Processing: Provides standardized processing of epigenomic and methylomic datasets to enable high allelic resolution comparisons across samples and species.
  • Empirical Validation: Applied to mouse embryonic datasets and human brain epigenomic data to identify dynamically methylated loci and allele-specific enrichment patterns.

Scientific Applications:

  • Imprinted Gene Regulation: Enables genome-wide identification and characterization of allele-specific DNAme and histone modification patterns at imprinted loci.
  • Developmental Biology: Supports analysis of allelic epigenetic regulation in mammalian development, including mouse embryonic datasets.
  • Neuroepigenomics: Facilitates detection of allele-specific H3K27ac and DNAme patterns in human brain epigenomic data.
  • Complex Genetic Disease Research: Allows investigation of allele-specific expression and epigenetic variation relevant to genetic and epigenetic disease mechanisms.

Methodology:

The pipeline processes input datasets using INDEL-aware algorithms that incorporate SNVs and INDELs to generate allele-specific DNA methylation maps and integrates these maps with RNA-seq and ChIP-seq epigenomic data.

Topics

Details

License:
MIT
Maturity:
Mature
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux
Programming Languages:
Python
Added:
6/11/2019
Last Updated:
11/24/2024

Operations

Publications

Richard Albert J, Koike T, Younesy H, Thompson R, Bogutz AB, Karimi MM, Lorincz MC. Development and application of an integrated allele-specific pipeline for methylomic and epigenomic analysis (MEA). BMC Genomics. 2018;19(1). doi:10.1186/s12864-018-4835-2. PMID:29907088. PMCID:PMC6003194.

PMID: 29907088
PMCID: PMC6003194
Funding: - Canadian Institutes of Health Research: MOP-133417 - Natural Sciences and Engineering Research Council of Canada: RGPIN-2015-05228

Documentation

Links