methylFlow

methylFlow reconstructs cell-specific DNA methylation patterns from high-throughput bisulfite-converted DNA sequencing data to characterize epigenetic heterogeneity in tumor samples.


Key Features:

  • Reconstruction of Heterogeneous Methylation Patterns: Assembles cell-specific methylation patterns from high-throughput bisulfite-converted sequencing reads to resolve methylation heterogeneity in heterogeneous tumor samples, including colon cancer.
  • Analysis of Clonal and Population Heterogeneity: Analyzes clonal and population-level heterogeneity across high-coverage sequencing data from multiple samples to elucidate relationships between clonal structure and population diversity in tumors.
  • Network Flow Problem Solving: Formulates and solves specific classes of minimum cost network flow problems to enable efficient and accurate reconstruction of methylation patterns across cell populations.

Scientific Applications:

  • Cancer Research: Identifies genomic regions with differential methylation between tumor and normal tissue, applied to the colon cancer epigenome to study how methylation aberrations contribute to gene expression heterogeneity and tumor development.
  • Epigenetic Studies: Dissects population-level DNA methylation dynamics and heterogeneity across various cancer types to support broader epigenomic analyses.

Methodology:

Processes high-throughput bisulfite-converted DNA sequencing data and reconstructs cell-specific methylation patterns by solving specific classes of minimum cost network flow problems.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux
Programming Languages:
R, C++
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Data Inputs & Outputs

Methylation analysis

Outputs

    Publications

    Dorri F, Mendelowitz L, Corrada Bravo H. methylFlow: cell-specific methylation pattern reconstruction from high-throughput bisulfite-converted DNA sequencing. Bioinformatics. 2016;32(11):1618-1624. doi:10.1093/bioinformatics/btw287. PMID:27246923. PMCID:PMC4892417.

    Documentation

    Links