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
Issue tracker
https://github.com/julienrichardalbert/MEA/issues