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Sneddon, A.

Publications and source records attributed to Sneddon, A..

2 recordsLinked to original sources

Real-time biochemical-free targeted sequencing of RNA species with RISER

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 reduced their respective read counts by more than 85%, resulting in an increase in sequencing depth of up to 93% for long non-coding RNAs. We also applied RISER for the depletion of globin mRNA in whole blood, achieving a decrease in globin reads by more than 90% as well as a significant increase in non-globin reads. Furthermore, using a GPU or a CPU, RISER is faster than GPU-accelerated basecalling and mapping. RISERs 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.

bioinformatics↗

Language-Informed Basecalling Architecture for Nanopore Direct RNA Sequencing

Algorithms developed for basecalling Nanopore signals have primarily focused on DNA to date and utilise the raw signal as the only input. However, it is known that messenger RNA (mRNA), which dominates Nanopore direct RNA (dRNA) sequencing libraries, contains specific nucleotide patterns that are implicitly encoded in the Nanopore signals since RNA is always sequenced from the 3 to 5 direction. In this study we present an approach to exploit the sequence biases in mRNA as an additional input to dRNA basecalling. We developed a probabilistic model of mRNA language and propose a modified CTC beam search decoding algorithm to conditionally incorporate the language model during basecalling. Our findings demonstrate that inclusion of mRNA language is able to guide CTC beam search decoding towards the more probable nucleotide sequence. We also propose a time efficient approach to decoding variable length nanopore signals. This work provides the first demonstration of the potential for biological language to inform Nanopore basecalling. Code is available at: https://github.com/comprna/radian.

bioinformatics↗