WellMeth is a integrated framework for Reduced Representation Bisulfite-Seq analysis

Features

  • Expands the Genotyping by Sequencing (GBS) approach to the detection of methylated cytosines in genomic DNA
  • Relies on the availability of high-quality reference genomes and for library construction double restriction digest with two methylation-insensitive enzymes is recommended
  • For paired-end short-read sequencing asymmetric forward- and reverse adapters will be applied with 4 to 6 nt long barcodes and a fixed number of random nucleotides (Unique Molecular Identifiers, UMIs) adjacent to the barcodes
  • UMI information will be used for post-alignment identification of PCR duplicates
  • Consists of four overlaying modules: Preprocessing, Mapping, Methylation variant detection and Differential methylation
  • Modules are interconnected by customizable wrapper scripts allowing fully automated execution
  • Fast, accurate and lightweight

Project Activity

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Categories

Bio-Informatics

License

Creative Commons Attribution ShareAlike License V3.0

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Additional Project Details

Operating Systems

Linux

Languages

English

User Interface

Console/Terminal

Registered

2020-05-08