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Single-cell RNA-seq analysis of mouse preimplantation embryos by third-generation sequencing.


ABSTRACT: The development of next generation sequencing (NGS) platform-based single-cell RNA sequencing (scRNA-seq) techniques has tremendously changed biological researches, while there are still many questions that cannot be addressed by them due to their short read lengths. We developed a novel scRNA-seq technology based on third-generation sequencing (TGS) platform (single-cell amplification and sequencing of full-length RNAs by Nanopore platform, SCAN-seq). SCAN-seq exhibited high sensitivity and accuracy comparable to NGS platform-based scRNA-seq methods. Moreover, we captured thousands of unannotated transcripts of diverse types, with high verification rate by reverse transcription PCR (RT-PCR)-coupled Sanger sequencing in mouse embryonic stem cells (mESCs). Then, we used SCAN-seq to analyze the mouse preimplantation embryos. We could clearly distinguish cells at different developmental stages, and a total of 27,250 unannotated transcripts from 9,338 genes were identified, with many of which showed developmental stage-specific expression patterns. Finally, we showed that SCAN-seq exhibited high accuracy on determining allele-specific gene expression patterns within an individual cell. SCAN-seq makes a major breakthrough for single-cell transcriptome analysis field.

SUBMITTER: Fan X 

PROVIDER: S-EPMC7773192 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Single-cell RNA-seq analysis of mouse preimplantation embryos by third-generation sequencing.

Fan Xiaoying X   Tang Dong D   Liao Yuhan Y   Li Pidong P   Zhang Yu Y   Wang Minxia M   Liang Fan F   Wang Xiao X   Gao Yun Y   Wen Lu L   Wang Depeng D   Wang Yang Y   Tang Fuchou F  

PLoS biology 20201230 12


The development of next generation sequencing (NGS) platform-based single-cell RNA sequencing (scRNA-seq) techniques has tremendously changed biological researches, while there are still many questions that cannot be addressed by them due to their short read lengths. We developed a novel scRNA-seq technology based on third-generation sequencing (TGS) platform (single-cell amplification and sequencing of full-length RNAs by Nanopore platform, SCAN-seq). SCAN-seq exhibited high sensitivity and acc  ...[more]

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