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Dogme: A tool for reanalyzing RNA and DNA modifications using nanopore sequencing

Updated

Abstract

An average of 147,879 m6A RNA modification sites were detected per replicate using the Dogme workflow.

  • Dogme automates the analysis of ONT sequencing data for RNA and DNA modifications.
  • The workflow integrates basecalling, read mapping, and modification detection in a standardized manner.
  • Detection of various RNA modifications, including m6A and m5C, was achieved with high reproducibility.
  • Comprehensive analysis supported direct RNA, complementary DNA, and genomic DNA sequencing data.
  • The pipeline produced consistent modification profiles and transcript expression levels across multiple mouse replicates.

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