Xu Ziye, Lyu Yuexiao, Chen Haide, Chen Yu, Wang Yongcheng
Department of Laboratory Medicine of The First Affiliated Hospital & Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, China.
Zhejiang Key Laboratory of Clinical In Vitro Diagnostic Techniques, Hangzhou, China.
Nat Protoc. 2025 Apr 25. doi: 10.1038/s41596-025-01170-8.
Formalin-fixed paraffin-embedded (FFPE) samples represent a vast and valuable resource of patient material, often linked to extensive clinical history and follow-up data. However, achieving single-cell or single-nucleus RNA (sc/snRNA) profiling in these archived tissues remains challenging. To address this, we have developed snRandom-seq, a droplet- and random primer-based single-nucleus total RNA sequencing technology specifically designed for FFPE tissues. This method captures total RNAs by using random primers and demonstrates a low doublet rate (0.3%), increased RNA coverage and enhanced detection of non-coding and nascent RNAs compared to state-of-the-art high-throughput sc/snRNA-seq technologies. This protocol provides a comprehensive guide to isolating single nuclei from FFPE samples; performing in situ DNA blocking, reverse transcription and dA tailing reactions; barcoding single-nucleus droplets; and preparing sequencing libraries. The entire snRandom-seq process can be completed in 4 d. This platform serves as a powerful tool for snRNA-seq of clinical specimens, with broad applications in studying complex biological systems.
福尔马林固定石蜡包埋(FFPE)样本是大量宝贵的患者材料资源,通常与详尽的临床病史和随访数据相关联。然而,在这些存档组织中实现单细胞或单细胞核RNA(sc/snRNA)分析仍然具有挑战性。为解决这一问题,我们开发了snRandom-seq,这是一种基于液滴和随机引物的单细胞核全RNA测序技术,专为FFPE组织设计。该方法通过使用随机引物捕获总RNA,与最先进的高通量sc/snRNA测序技术相比,具有较低的双细胞率(0.3%)、更高的RNA覆盖率以及对非编码RNA和新生RNA更强的检测能力。本方案提供了从FFPE样本中分离单细胞核、进行原位DNA封闭、逆转录和dA加尾反应、对单细胞核液滴进行条形码标记以及制备测序文库的全面指南。整个snRandom-seq过程可在4天内完成。该平台是临床样本snRNA测序的强大工具,在研究复杂生物系统方面具有广泛应用。