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Biochemical-free enrichment or depletion of RNA classes in real-time during direct RNA sequencing with RISER

Author

Listed:
  • Alexandra Sneddon

    (EMBL Australia Partner Laboratory Network at the Australian National University
    Australian National University
    Australian National University)

  • Agin Ravindran

    (EMBL Australia Partner Laboratory Network at the Australian National University
    Australian National University
    Australian National University)

  • Somasundhari Shanmuganandam

    (Australian National University
    Australian National University)

  • Madhu Kanchi

    (Australian National University)

  • Nadine Hein

    (Australian National University)

  • Simon Jiang

    (Australian National University
    Australian National University
    The Canberra Hospital)

  • Nikolay Shirokikh

    (Australian National University)

  • Eduardo Eyras

    (EMBL Australia Partner Laboratory Network at the Australian National University
    Australian National University
    Australian National University)

Abstract

The heterogeneous composition of cellular transcriptomes poses a major challenge for detecting weakly expressed RNA classes, as they can be obscured by abundant RNAs. Although biochemical protocols can enrich or deplete specified RNAs, they are time-consuming, expensive and can compromise RNA integrity. Here we introduce RISER, a biochemical-free technology for the real-time enrichment or depletion of RNA classes. RISER performs selective rejection of molecules during direct RNA sequencing by identifying RNA classes directly from nanopore signals with deep learning and communicating with the sequencing hardware in real time. By targeting the dominant messenger and mitochondrial RNA classes for depletion, RISER reduces their respective read counts by more than 85%, resulting in an increase in sequencing depth of 47% on average for long non-coding RNAs. We also apply RISER for the depletion of globin mRNA in whole blood, achieving a decrease in globin reads by more than 90% as well as an increase in non-globin reads by 16% on average. Furthermore, using a GPU or a CPU, RISER is faster than GPU-accelerated basecalling and mapping. RISER’s modular and retrainable software and intuitive command-line interface allow easy adaptation to other RNA classes. RISER is available at https://github.com/comprna/riser .

Suggested Citation

  • Alexandra Sneddon & Agin Ravindran & Somasundhari Shanmuganandam & Madhu Kanchi & Nadine Hein & Simon Jiang & Nikolay Shirokikh & Eduardo Eyras, 2024. "Biochemical-free enrichment or depletion of RNA classes in real-time during direct RNA sequencing with RISER," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48673-8
    DOI: 10.1038/s41467-024-48673-8
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    References listed on IDEAS

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    1. Felice-Alessio Bava & Carolina Eliscovich & Pedro G. Ferreira & Belen Miñana & Claudia Ben-Dov & Roderic Guigó & Juan Valcárcel & Raúl Méndez, 2013. "CPEB1 coordinates alternative 3′-UTR formation with translational regulation," Nature, Nature, vol. 495(7439), pages 121-125, March.
    2. Charlotte Soneson & Yao Yao & Anna Bratus-Neuenschwander & Andrea Patrignani & Mark D. Robinson & Shobbir Hussain, 2019. "A comprehensive examination of Nanopore native RNA sequencing for characterization of complex transcriptomes," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
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