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使用 FLASH-seq 进行快速且高度灵敏的全长单细胞 RNA 测序。

Fast and highly sensitive full-length single-cell RNA sequencing using FLASH-seq.

机构信息

Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.

Department of Ophthalmology, University of Basel, Basel, Switzerland.

出版信息

Nat Biotechnol. 2022 Oct;40(10):1447-1451. doi: 10.1038/s41587-022-01312-3. Epub 2022 May 30.

DOI:10.1038/s41587-022-01312-3
PMID:35637419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9546769/
Abstract

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.

摘要

我们提出了 FLASH-seq(FS)方法,与 Smart-seq3 相比,该方法具有更高的灵敏度和更低的人工操作时间,可实现全长单细胞 RNA 测序(scRNA-seq)。整个 FS 方案可在~4.5 小时内完成,易于自动化,并可轻松微型化以减少资源消耗。FS 方案还可以使用独特的分子标识符(UMIs)进行分子计数,同时显示减少的链入侵伪影。FS 将特别有助于在多个样本中以高分辨率描述基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5194/9546769/ac495d5d45e7/41587_2022_1312_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5194/9546769/6c30ac4d590e/41587_2022_1312_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5194/9546769/ac495d5d45e7/41587_2022_1312_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5194/9546769/6c30ac4d590e/41587_2022_1312_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5194/9546769/ac495d5d45e7/41587_2022_1312_Fig2_HTML.jpg

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