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整合中胚层诱导胚胎干细胞的单细胞转录组、染色质可及性和多组学分析。

Integrating single-cell transcriptomes, chromatin accessibility, and multiomics analysis of mesoderm-induced embryonic stem cells.

作者信息

Ko Kyung Dae, Jiang Kan, Dell'Orso Stefania, Sartorelli Vittorio

机构信息

Laboratory of Muscle Stem Cells and Gene Regulation, NIAMS, NIH, Bethesda, MD, USA.

Biodata Mining and Discovery Section, NIAMS, NIH, Bethesda, MD, USA.

出版信息

STAR Protoc. 2023 May 15;4(2):102307. doi: 10.1016/j.xpro.2023.102307.

DOI:10.1016/j.xpro.2023.102307
PMID:37192048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10199178/
Abstract

Here, we present workflows for integrating independent transcriptomic and chromatin accessibility datasets and analyzing multiomics. First, we describe steps for integrating independent transcriptomic and chromatin accessibility measurements. Next, we detail multimodal analysis of transcriptomes and chromatin accessibility performed in the same sample. We demonstrate their use by analyzing datasets obtained from mouse embryonic stem cells induced to differentiate toward mesoderm-like, myogenic, or neurogenic phenotypes. For complete details on the use and execution of this protocol, please refer to Khateb et al..

摘要

在此,我们展示了整合独立转录组学和染色质可及性数据集以及分析多组学的工作流程。首先,我们描述整合独立转录组学和染色质可及性测量的步骤。接下来,我们详细介绍在同一样本中进行的转录组和染色质可及性的多模态分析。我们通过分析从小鼠胚胎干细胞诱导分化为中胚层样、成肌或神经源性表型所获得的数据集来展示它们的用途。有关本方案使用和执行的完整详细信息,请参考Khateb等人的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/a6c47709bf63/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/433ab9a7af18/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/647376b78ef4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/0b66a41c8af9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/0db8e8f2b9c1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/498ac29fab60/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/deb7ac9ce36d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/4b0ba62c7516/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/a6c47709bf63/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/433ab9a7af18/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/647376b78ef4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/0b66a41c8af9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/0db8e8f2b9c1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/498ac29fab60/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/deb7ac9ce36d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/4b0ba62c7516/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ada/10199178/a6c47709bf63/gr7.jpg

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本文引用的文献

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Cell Rep. 2022 Aug 16;40(7):111219. doi: 10.1016/j.celrep.2022.111219.
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Single-cell chromatin state analysis with Signac.使用 Signac 进行单细胞染色质状态分析。
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