蛋白质组
转录组
表观基因组
计算生物学
蛋白质组学
生物
单细胞分析
基因组
基因
细胞
遗传学
基因表达
DNA甲基化
作者
James Fulcher,Lye Meng Markillie,Hugh Mitchell,Sarah Williams,Kristin Engbrecht,Ronald J. Moore,Joshua Cantlon-Bruce,Johannes W. Bagnoli,Anjali Seth,Ljiljana Paša‐Tolić,Ying Zhu
标识
DOI:10.1101/2022.05.17.492137
摘要
ABSTRACT Single-cell multiomics can provide comprehensive insights into gene regulatory networks, cellular diversity, and temporal dynamics. While tools for co-profiling the single-cell genome, transcriptome, and epigenome are available, accessing the proteome in parallel is more challenging. To overcome this limitation, we developed nanoSPLITS (nanodroplet SPlitting for Linked-multimodal Investigations of Trace Samples), a platform that enables unbiased measurement of the transcriptome and proteome from same single cells using RNA sequencing and mass spectrometry-based proteomics, respectively. We demonstrated the nanoSPLITS can robustly profile > 5000 genes and > 2000 proteins per single cell, and identify cell-type-specific markers from both modalities.
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