生物
转录组
小核RNA
核糖核酸
电池类型
核心
细胞核
细胞
单细胞分析
基因
RNA序列
RNA剪接
基因表达
细胞生物学
计算生物学
基因表达谱
遗传学
非编码RNA
作者
Trygve E. Bakken,Rebecca D. Hodge,Jeremy A. Miller,Zizhen Yao,Thuc Nghi Nguyen,Brian D. Aevermann,Eliza Barkan,Darren Bertagnolli,Tamara Casper,Nick Dee,Emma Garren,Jeff Goldy,Lucas T. Graybuck,Matthew Kroll,Roger S. Lasken,Kanan Lathia,Sheana Parry,Christine Rimorin,Richard H. Scheuermann,Nicholas J. Schork
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2018-12-26
卷期号:13 (12): e0209648-e0209648
被引量:641
标识
DOI:10.1371/journal.pone.0209648
摘要
Transcriptomic profiling of complex tissues by single-nucleus RNA-sequencing (snRNA-seq) affords some advantages over single-cell RNA-sequencing (scRNA-seq). snRNA-seq provides less biased cellular coverage, does not appear to suffer cell isolation-based transcriptional artifacts, and can be applied to archived frozen specimens. We used well-matched snRNA-seq and scRNA-seq datasets from mouse visual cortex to compare cell type detection. Although more transcripts are detected in individual whole cells (~11,000 genes) than nuclei (~7,000 genes), we demonstrate that closely related neuronal cell types can be similarly discriminated with both methods if intronic sequences are included in snRNA-seq analysis. We estimate that the nuclear proportion of total cellular mRNA varies from 20% to over 50% for large and small pyramidal neurons, respectively. Together, these results illustrate the high information content of nuclear RNA for characterization of cellular diversity in brain tissues.
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