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treekoR:通过阐明高维细胞仪数据中的层次关系来识别细胞表型关联。

treekoR: identifying cellular-to-phenotype associations by elucidating hierarchical relationships in high-dimensional cytometry data.

机构信息

School of Mathematics and Statistics, The University of Sydney, Sydney, New South Wales, Australia.

Charles Perkins Centre, The University of Sydney, Sydney, New South Wales, Australia.

出版信息

Genome Biol. 2021 Nov 29;22(1):324. doi: 10.1186/s13059-021-02526-5.

DOI:10.1186/s13059-021-02526-5
PMID:34844647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8628061/
Abstract

High-throughput single-cell technologies hold the promise of discovering novel cellular relationships with disease. However, analytical workflows constructed for these technologies to associate cell proportions with disease often employ unsupervised clustering techniques that overlook the valuable hierarchical structures that have been used to define cell types. We present treekoR, a framework that empirically recapitulates these structures, facilitating multiple quantifications and comparisons of cell type proportions. Our results from twelve case studies reinforce the importance of quantifying proportions relative to parent populations in the analyses of cytometry data - as failing to do so can lead to missing important biological insights.

摘要

高通量单细胞技术有望发现与疾病相关的新型细胞关系。然而,为将细胞比例与疾病相关联而构建的这些技术的分析工作流程通常采用无监督聚类技术,而忽略了已用于定义细胞类型的有价值的层次结构。我们提出了 treekoR,这是一个经验上再现这些结构的框架,促进了细胞类型比例的多种量化和比较。我们从十二个案例研究中得出的结果,强调了在分析细胞测定数据时相对于父群体进行比例量化的重要性 - 因为未能这样做可能会导致错过重要的生物学见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/7f36f5f42bfc/13059_2021_2526_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/4976c34db606/13059_2021_2526_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/3c350f426618/13059_2021_2526_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/0b662b10a6ad/13059_2021_2526_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/7f36f5f42bfc/13059_2021_2526_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/4976c34db606/13059_2021_2526_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/3c350f426618/13059_2021_2526_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/0b662b10a6ad/13059_2021_2526_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873e/8628450/7f36f5f42bfc/13059_2021_2526_Fig4_HTML.jpg

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本文引用的文献

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A streamlined whole blood CyTOF workflow defines a circulating immune cell signature of COVID-19.一种简化的全血 CyTOF 工作流程定义了 COVID-19 的循环免疫细胞特征。
Cytometry A. 2021 May;99(5):446-461. doi: 10.1002/cyto.a.24317. Epub 2021 Feb 16.
3
Increased IL-10-producing regulatory T cells are characteristic of severe cases of COVID-19.
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Clin Transl Immunology. 2020 Nov 13;9(11):e1204. doi: 10.1002/cti2.1204. eCollection 2020.
4
Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications.深度免疫剖析 COVID-19 患者,揭示具有治疗意义的不同免疫类型。
Science. 2020 Sep 4;369(6508). doi: 10.1126/science.abc8511. Epub 2020 Jul 15.
5
Marked T cell activation, senescence, exhaustion and skewing towards TH17 in patients with COVID-19 pneumonia.COVID-19 肺炎患者中标记的 T 细胞激活、衰老、衰竭和向 TH17 的倾斜。
Nat Commun. 2020 Jul 6;11(1):3434. doi: 10.1038/s41467-020-17292-4.
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Deep immune profiling of patients treated with lenalidomide and dexamethasone with or without daratumumab.来那度胺和地塞米松联合或不联合达雷妥尤单抗治疗患者的深度免疫分析。
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