Nature Biotechnology ( IF 33.1 ) Pub Date : 2022-05-30 , DOI: 10.1038/s41587-022-01312-3 Vincent Hahaut 1, 2 , Dinko Pavlinic 1, 2 , Walter Carbone 3 , Sven Schuierer 3 , Pierre Balmer 1, 2 , Mathieu Quinodoz 1, 2 , Magdalena Renner 1, 2 , Guglielmo Roma 3 , Cameron S Cowan 1, 2 , Simone Picelli 1, 2
We present FLASH-seq (FS), a full-length single-cell RNA sequencing (scRNA-seq) method with increased sensitivity and reduced hands-on time compared to Smart-seq3. The entire FS protocol can be performed in ~4.5 hours, is simple to automate and can be easily miniaturized to decrease resource consumption. The FS protocol can also use unique molecular identifiers (UMIs) for molecule counting while displaying reduced strand-invasion artifacts. FS will be especially useful for characterizing gene expression at high resolution across multiple samples.
中文翻译:
使用 FLASH-seq 进行快速、高灵敏度的全长单细胞 RNA 测序
我们推出了 FLASH-seq (FS),这是一种全长单细胞 RNA 测序 (scRNA-seq) 方法,与 Smart-seq3 相比,其灵敏度更高,操作时间更短。整个 FS 协议可以在约 4.5 小时内完成,易于自动化,并且可以轻松小型化以减少资源消耗。 FS 协议还可以使用独特的分子标识符 (UMI) 进行分子计数,同时显示减少的链侵入伪影。 FS 对于以高分辨率表征多个样本的基因表达尤其有用。