Real-time molecular classification of leukemias
Mélanie Sagniez, Shawn M. Simpson, Maxime CaroniD, Marieke J. RozendaaliD, Bastien Paré, Thomas SontagiD, Sylvie Langlois, Alexandre RouetteiD, Vincent‐Philippe LavalléeiD, Sonia CellotiD, Daniel SinnettiD, Thai Hoa TraniD, Martin A. SmithiD
Abstract
Gene expression profiling provides a detailed molecular snapshot of cellular phenotypes that can be used to compare different biological conditions. Nanopore sequencing technology can generate high-resolution transcriptomic data in real-time and at low cost, which heralds new opportunities for molecular medicine. In this study, we demonstrate the clinical utility of real-time transcriptomic profiling by processing RNA sequencing data from childhood acute lymphoblastic leukemia (ALL) patients on-the-fly with a trained neural network classifier. This strategy successfully distinguished 11/12 representative ALL molecular subtypes and one non-leukemia control in as little as 5 minutes of sequencing on a MinION sequencer or in less than 1 hour on disposable, low cost Flongle flow cells. Our findings suggest that real-time transcriptomics constitutes a drastically efficient solution for the molecular diagnosis of ALL and other diseases, where conventional clinical workflows require days if not weeks to achieve similar results.
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