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Biochemical-free enrichment or depletion of RNA classes in real-time during direct RNA sequencing with RISER.
Sneddon, Alexandra; Ravindran, Agin; Shanmuganandam, Somasundhari; Kanchi, Madhu; Hein, Nadine; Jiang, Simon; Shirokikh, Nikolay; Eyras, Eduardo.
Afiliação
  • Sneddon A; EMBL Australia Partner Laboratory Network at the Australian National University, Canberra, ACT 2601, Australia.
  • Ravindran A; Centre for Computational Biomedical Sciences, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Shanmuganandam S; The Shine-Dalgarno Centre for RNA Innovation, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Kanchi M; EMBL Australia Partner Laboratory Network at the Australian National University, Canberra, ACT 2601, Australia.
  • Hein N; Centre for Computational Biomedical Sciences, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Jiang S; The Shine-Dalgarno Centre for RNA Innovation, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Shirokikh N; Department of Immunity, Inflammation and Infection, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia.
  • Eyras E; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra, ACT 2601, Australia.
Nat Commun ; 15(1): 4422, 2024 May 24.
Article em En | MEDLINE | ID: mdl-38789440
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 .
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Análise de Sequência de RNA Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Análise de Sequência de RNA Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália