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IsoCirc catalogs full-length circular RNA isoforms in human transcriptomes.


ABSTRACT: Circular RNAs (circRNAs) have emerged as an important class of functional RNA molecules. Short-read RNA sequencing (RNA-seq) is a widely used strategy to identify circRNAs. However, an inherent limitation of short-read RNA-seq is that it does not experimentally determine the full-length sequences and exact exonic compositions of circRNAs. Here, we report isoCirc, a strategy for sequencing full-length circRNA isoforms, using rolling circle amplification followed by nanopore long-read sequencing. We describe an integrated computational pipeline to reliably characterize full-length circRNA isoforms using isoCirc data. Using isoCirc, we generate a comprehensive catalog of 107,147 full-length circRNA isoforms across 12 human tissues and one human cell line (HEK293), including 40,628 isoforms ≥500 nt in length. We identify widespread alternative splicing events within the internal part of circRNAs, including 720 retained intron events corresponding to a class of exon-intron circRNAs (EIciRNAs). Collectively, isoCirc and the companion dataset provide a useful strategy and resource for studying circRNAs in human transcriptomes.

SUBMITTER: Xin R 

PROVIDER: S-EPMC7803736 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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isoCirc catalogs full-length circular RNA isoforms in human transcriptomes.

Xin Ruijiao R   Gao Yan Y   Gao Yuan Y   Wang Robert R   Kadash-Edmondson Kathryn E KE   Liu Bo B   Wang Yadong Y   Lin Lan L   Xing Yi Y  

Nature communications 20210112 1


Circular RNAs (circRNAs) have emerged as an important class of functional RNA molecules. Short-read RNA sequencing (RNA-seq) is a widely used strategy to identify circRNAs. However, an inherent limitation of short-read RNA-seq is that it does not experimentally determine the full-length sequences and exact exonic compositions of circRNAs. Here, we report isoCirc, a strategy for sequencing full-length circRNA isoforms, using rolling circle amplification followed by nanopore long-read sequencing.  ...[more]

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