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Advances in long-read single-cell transcriptomics

delete2024-05-24
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OA
AI
P
Pallawi Kumari
M
Manmeet Kaur
K
Kiran Dindhoria
B
Bruce Ashford
S
Shanika L. Amarasinghe
A
Amarinder Singh Thind *
DOI:10.1007/s00439-024-02678-xdelete
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Abstract

Abstract

En 中文
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.
Keywords:
RNA-SEQ
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Human Genetics cover
Human Genetics
IF:
3.6
Papers:
4.6K
Citations:
8.9K

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Monash University
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