Abstract
Long-read single-cell transcriptomics (scRNA-Seq) is revolutionizing the way we profile heterogeneity in disease. Traditional short-read scRNA-Seq methods are limited in their ability to provide complete transcript coverage, resolve isoforms, and identify novel transcripts. The scRNA-Seq protocols developed for long-read sequencing platforms overcome these limitations by enabling the characterization of full-length transcripts. Long-read scRNA-Seq techniques initially suffered from comparatively poor accuracy compared to short read scRNA-Seq. However, with improvements in accuracy, accessibility, and cost efficiency, long-reads are gaining popularity in the field of scRNA-Seq. This review details the advances in long-read scRNA-Seq, with an emphasis on library preparation protocols and downstream bioinformatics analysis tools.
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CITATION STYLE
Kumari, P., Kaur, M., Dindhoria, K., Ashford, B., Amarasinghe, S. L., & Thind, A. S. (2024, October 1). Advances in long-read single-cell transcriptomics. Human Genetics. Springer Science and Business Media Deutschland GmbH. https://doi.org/10.1007/s00439-024-02678-x
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