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<p>Chimera artifacts in nanopore direct RNA sequencing (dRNA-seq) introduce substantial inaccuracies, complicating downstream applications such as transcript annotation and gene fusion detection. Current basecalling models are unable to detect or mitigate these artifacts, limiting the reliability and utility of dRNA-seq for transcriptomics research. To address this challenge, we present DeepChopper, a genomic language model specifically designed to identify and remove adapter sequences from base-called dRNA-seq long reads with single-base precision. Operating independently of raw signal or alignment information, DeepChopper effectively eliminates adapter-bridged artifacts. Here, we show that DeepChopper enhances the accuracy of downstream analyses and unlocks the full potential of nanopore dRNA-seq, establishing it as a more robust tool for diverse transcriptomics applications.</p>

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Genomic language model mitigates chimera artifacts in nanopore direct RNA sequencing

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年1月19日

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  • Yangyang Li,
  • Ting-You Wang,
  • Qingxiang Guo,
  • Yanan Ren,
  • Xiaotong Lu,
  • Qi Cao,
  • Rendong Yang

摘要

Chimera artifacts in nanopore direct RNA sequencing (dRNA-seq) introduce substantial inaccuracies, complicating downstream applications such as transcript annotation and gene fusion detection. Current basecalling models are unable to detect or mitigate these artifacts, limiting the reliability and utility of dRNA-seq for transcriptomics research. To address this challenge, we present DeepChopper, a genomic language model specifically designed to identify and remove adapter sequences from base-called dRNA-seq long reads with single-base precision. Operating independently of raw signal or alignment information, DeepChopper effectively eliminates adapter-bridged artifacts. Here, we show that DeepChopper enhances the accuracy of downstream analyses and unlocks the full potential of nanopore dRNA-seq, establishing it as a more robust tool for diverse transcriptomics applications.