基因亚型
核糖核酸
生物
计算生物学
转录组
等位基因
生物信息学
基因
外显子
细胞
遗传学
基因表达
RNA序列
作者
Michael Hagemann-Jensen,Christoph Ziegenhain,Ping Chen,Daniel Ramsköld,Gert‐Jan Hendriks,Anton J. M. Larsson,Omid R. Faridani,Rickard Sandberg
标识
DOI:10.1038/s41587-020-0497-0
摘要
Large-scale sequencing of RNA from individual cells can reveal patterns of gene, isoform and allelic expression across cell types and states1. However, current short-read single-cell RNA-sequencing methods have limited ability to count RNAs at allele and isoform resolution, and long-read sequencing techniques lack the depth required for large-scale applications across cells2,3. Here we introduce Smart-seq3, which combines full-length transcriptome coverage with a 5′ unique molecular identifier RNA counting strategy that enables in silico reconstruction of thousands of RNA molecules per cell. Of the counted and reconstructed molecules, 60% could be directly assigned to allelic origin and 30–50% to specific isoforms, and we identified substantial differences in isoform usage in different mouse strains and human cell types. Smart-seq3 greatly increased sensitivity compared to Smart-seq2, typically detecting thousands more transcripts per cell. We expect that Smart-seq3 will enable large-scale characterization of cell types and states across tissues and organisms. Smart-seq3 enables isoform- and allele-specific reconstruction of RNA molecules.
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