Single-cell nucleosome, methylome, and transcriptome (scNMT) sequencing is a recently developed method that allows multiomics profiling of single cells. In this scNMT protocol, we describe profiling of cells from mouse brain and pancreatic organoids, using liquid handling platforms to increase throughput from 96-well to 384-well plate format. Our approach miniaturizes reaction volumes and incorporates the latest Smart-seq3 protocol to obtain higher numbers of detected genes and genomic DNA (gDNA) CpGs per cell. We outline normalization steps to optimally distribute per-cell sequencing depth. For complete details on the use and execution of this protocol, please refer to Kremer et al. and other works.(1)(,)(2)(,)(3)(,)(4)(,)(5)(,)(6)(,)(7) This protocol is an update to Cerrizuela et al.(7).
Protocol update to: High-throughput scNMT protocol for multiomics profiling of single cells from mouse brain and pancreatic organoids.
方案更新:用于对小鼠脑和胰腺类器官的单个细胞进行多组学分析的高通量 scNMT 方案
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作者:Cerrizuela Santiago, Kaya Oguzhan, Kremer Lukas P M, Sarvari Andrea, Ellinger Tobias, Straub Jannes, Brunken Jan, Sanz-Morejón Andrés, Korkmaz Aylin, MartÃn-Villalba Ana
| 期刊: | STAR Protocols | 影响因子: | 1.300 |
| 时间: | 2025 | 起止号: | 2025 Jul 24; 6(3):103980 |
| doi: | 10.1016/j.xpro.2025.103980 | 种属: | Mouse |
| 研究方向: | 细胞生物学 | ||
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