Identification of cell barcodes from long-read single-cell RNA-seq with BLAZE
The University of Melbourne · Melbourne Genomics Health Alliance · +1 more institution
Abstract
Long-read single-cell RNA sequencing (scRNA-seq) enables the quantification of RNA isoforms in individual cells. However, long-read scRNA-seq using the Oxford Nanopore platform has largely relied upon matched short-read data to identify cell barcodes. We introduce BLAZE, which accurately and efficiently identifies 10x cell barcodes using only nanopore long-read scRNA-seq data. BLAZE outperforms the existing tools and provides an accurate representation of the cells present in long-read scRNA-seq when compared to matched short reads. BLAZE simplifies long-read scRNA-seq while improving the results, is compatible with downstream tools accepting a cell barcode file, and is available at…
Citation impact
- FWCI
- 25.00
- Percentile
- 100%
- References
- 46
Authors
7- YYYupei YouCorresponding
The University of Melbourne, Melbourne Genomics Health Alliance
- YDYair D. J. Prawer
The University of Melbourne
- RDRicardo De Paoli‐Iseppi
The University of Melbourne
- CPCameron P. J. Hunt
The University of Melbourne, Florey Institute of Neuroscience and Mental Health
- CLClare L. Parish
The University of Melbourne, Florey Institute of Neuroscience and Mental Health
Topics & keywords
- Barcode
- Nanopore sequencing
- Biology
- RNA
- Identification (biology)
- RNA-Seq
- Computational biology
- Single-cell analysis